1. Introduction
1.1. Overview of Diabetes and Its Complications
Diabetes, a chronic metabolic disorder characterized by impaired insulin production or utilization, has reached epidemic proportions worldwide. The disease affects millions of individuals, imposing a significant burden on healthcare systems and economies. Diabetes is associated with various complications that significantly impact the quality of life and increase morbidity and mortality rates among affected individuals [
1,
2].
Type 2 diabetes mellitus (T2DM) is the most prevalent form, accounting for approximately 90% of all diabetes cases [
3]. It arises due to a combination of insulin resistance and inadequate insulin secretion. T2DM is often associated with lifestyle factors such as sedentary behavior, unhealthy dietary habits, and obesity [
4]. On the other hand, type 1 diabetes (T1DM) is an autoimmune condition characterized by the destruction of insulin-producing beta cells in the pancreas, resulting in absolute insulin deficiency [
5]. Other forms of diabetes, such as gestational diabetes, also pose significant health risks, particularly to pregnant women and their offspring [
6].
The complications associated with diabetes are diverse and affect multiple organ systems. Chronic hyperglycemia in diabetes leads to the development of microvascular and macrovascular complications. Microvascular complications primarily affect the small blood vessels, including the eyes (diabetic retinopathy), kidneys (diabetic nephropathy), and nerves (diabetic neuropathy). Macrovascular complications involve the large blood vessels and contribute to an increased risk of cardiovascular diseases such as coronary artery disease, stroke, and peripheral arterial disease [
7,
8].
These complications can result in severe health consequences, including visual impairment, end-stage renal disease, lower limb amputations, and cardiovascular events [
9]. Moreover, diabetes is associated with a higher risk of other conditions such as hypertension, dyslipidemia, and non-alcoholic fatty liver disease, further exacerbating the overall disease burden [
10].
The management of diabetes and its complications requires a comprehensive approach, including lifestyle modifications, glucose-lowering medications, and targeted interventions to address specific complications. While advancements have been made in conventional diabetes management, there is a growing interest in exploring alternative therapeutic strategies that offer improved efficacy, fewer side effects, and disease-modifying potential [
11,
12].
In this context, natural products and their derivatives have gained significant attention as potential agents for diabetes management. These compounds, derived from various sources including plants, fungi, marine organisms, and algae, possess diverse chemical constituents and exhibit a wide range of pharmacological activities [
13,
14]. Exploiting the potential of natural products in diabetes research holds promise for the development of novel therapeutics and interventions that can effectively control blood glucose levels and mitigate the complications associated with the disease [
15,
16].
This review article aims to provide a comprehensive overview of the promise of natural products and their derivatives, specifically derived from algae, in diabetes and its complications. By exploring present advancements and future prospects, we seek to contribute to the understanding and development of innovative approaches for diabetes management.
1.2. Importance of Natural Products and Their Derivatives in Diabetes Management
The management of diabetes, a chronic metabolic disorder affecting millions worldwide, presents a formidable challenge to healthcare systems globally. Conventional therapeutic approaches, although effective to a certain extent, often exhibit limitations such as side effects and inadequate disease control. Consequently, there is a growing interest in exploring alternative strategies that offer safer and more efficacious options for diabetes management [
17].
Natural products and their derivatives have garnered considerable attention in recent years as potential therapeutic agents for diabetes and its complications. These compounds, derived from diverse natural sources such as plants, animals, fungi, and microorganisms, offer a vast array of bioactive constituents with multifaceted pharmacological activities. Harnessing the potential of natural products in diabetes research not only provides a rich source of novel compounds but also capitalizes on traditional medicinal knowledge that has been passed down through generations [
18,
19].
One of the primary advantages of natural products is their extensive chemical diversity. Plants, including algae, for instance, produce an impressive array of secondary metabolites, including alkaloids, flavonoids, terpenoids, and phenolic compounds, which exhibit a wide range of biological activities [
20,
21]. These diverse chemical structures offer a valuable resource for the development of targeted therapies, allowing for the modulation of various molecular targets involved in glucose homeostasis, insulin secretion, and insulin sensitivity [
22].
Moreover, natural products often possess pleiotropic effects, meaning they can target multiple pathways simultaneously. This characteristic is particularly relevant in the complex pathophysiology of diabetes, where dysregulation occurs at multiple levels. By addressing various underlying mechanisms simultaneously, natural products and their derivatives hold the potential to provide comprehensive and synergistic benefits in diabetes management [
23,
24].
Another key advantage of natural products is their potential to mitigate the complications associated with diabetes. Chronic hyperglycemia leads to the generation of oxidative stress and the activation of inflammatory pathways, which contribute to the development of microvascular and macrovascular complications [
25]. Natural products, with their antioxidant and anti-inflammatory properties, offer a promising avenue for ameliorating these complications and preserving the health of affected individuals [
26].
Furthermore, natural products often exhibit a favorable safety profile compared to synthetic pharmaceutical agents. Many traditional medicinal systems have utilized natural products for centuries, highlighting their historical use and long-term safety record. This advantage is particularly relevant in chronic diseases like diabetes, where long-term management is necessary, and minimizing adverse effects is of paramount importance [
27,
28].
Thus, natural products and their derivatives hold great promise in the management of diabetes. Their diverse chemical constituents, pleiotropic effects, and potential to mitigate complications make them attractive candidates for the development of novel therapeutic approaches [
29]. By leveraging the power of natural products, we have the opportunity to expand our therapeutic armamentarium and improve outcomes for individuals living with diabetes [
30]. This review aims to provide a comprehensive overview of the role of natural products in diabetes management, highlighting their significance and potential for future advancements in the field.
1.3. Significance of Algae-Derived Natural Products in Diabetes Research
In recent years, there has been growing interest in exploring the potential of natural products as therapeutic agents for the management of diabetes. Among the various natural sources, algae have emerged as promising reservoirs of bioactive compounds with significant implications for diabetes research. Algae, photosynthetic organisms found in diverse aquatic habitats, possess a remarkable ability to synthesize an array of unique and biologically active compounds. These algae-derived natural products offer novel avenues for investigating the pathophysiology of diabetes and developing innovative interventions for its management [
31,
32].
The significance of algae-derived natural products in diabetes research lies in their potential to target multiple aspects of the disease. Algae produce a wide range of bioactive compounds such as polysaccharides, polyphenols, pigments, fatty acids, and sterols, which have demonstrated various pharmacological properties relevant to diabetes. These compounds can modulate glucose metabolism, enhance insulin sensitivity, improve lipid profiles, and exert antioxidant and anti-inflammatory effects, all of which are crucial factors in diabetes management [
33,
34].
Furthermore, algae-derived natural products show promise in addressing specific complications associated with diabetes. Diabetic retinopathy, a microvascular complication, is characterized by oxidative stress and inflammation in the retina. Algae-derived compounds, with their antioxidant and anti-inflammatory properties, have shown potential in protecting retinal cells and preventing the progression of retinopathy [
35,
36]. Similarly, algae-derived compounds have demonstrated reno-protective effects by reducing albuminuria, attenuating renal fibrosis, and modulating inflammatory pathways, providing a potential avenue for managing diabetic nephropathy [
37,
38].
The unique properties of algae-derived natural products make them attractive candidates for developing therapeutic interventions with improved efficacy and safety profiles. Algae can be easily cultured, offering a sustainable and scalable source of bioactive compounds. Moreover, algae exhibit a remarkable ability to synthesize structurally diverse compounds, some of which may have superior pharmacokinetic properties compared to synthetic counterparts. These characteristics open up possibilities for the development of novel drug candidates or natural product-derived formulations for diabetes management [
39,
40].
Besides, algae-derived natural products have the potential to complement existing diabetes treatments and fill therapeutic gaps. They can be used as adjuvants to conventional antidiabetic drugs, enhancing their efficacy or providing synergistic effects [
41,
42]. Additionally, natural products derived from algae may offer alternative therapeutic options for individuals who experience intolerance or resistance to current medications [
43].
Therefore, algae-derived natural products represent a significant and untapped resource for diabetes research and management. The diverse array of bioactive compounds synthesized by algae offers a rich source of potential therapeutic agents, capable of targeting various aspects of the disease and its complications [
33,
44]. Expanding our understanding of the significance and potential applications of algae-derived natural products in diabetes research holds promise for advancing therapeutic interventions and improving patient outcomes. This review article aims to provide an in-depth exploration of the role of algae-derived natural products in diabetes research, highlighting their significance and potential future directions in the field [
45,
46].
2. Algae as a Source of Natural Products
2.1. Introduction to Algae and Its Diversity
Algae, a diverse group of photosynthetic organisms, encompass a wide range of species found in aquatic environments such as oceans, lakes, rivers, and even damp terrestrial habitats. Algae can be classified into multiple taxonomic groups, including Cyanobacteria (blue-green algae), Chlorophyta (green algae), Ochrophyta/Phaeophyceae (brown algae), Rhodophyta (red algae), and Bacillariophyta (diatoms), among others not mentioned. This immense diversity of algae offers a vast and virtually untapped resource for the discovery and exploration of natural products with potential applications in various fields, including medicine, agriculture, and industry, etc. [
47,
48].
One of the distinguishing features of algae is their ability to undergo photosynthesis, utilizing sunlight to convert carbon dioxide and water into organic compounds. This photosynthetic capacity not only contributes to the oxygen production in our atmosphere but also enables algae to synthesize a wide array of unique and complex molecules [
48,
49]. Algae are known to produce a diverse range of bioactive compounds, including polysaccharides, proteins, pigments, lipids, sterols, terpenes, and phenolic compounds [
50].
Algae exhibit an impressive chemical diversity, driven by genetic variability and adaptation to different ecological niches. Each taxonomic group of algae possesses distinct metabolic pathways and biosynthetic capabilities, resulting in the synthesis of species-specific compounds [
51]. For example, red algae (Rhodophyta) are well-known for their production of sulfated polysaccharides, such as carrageenan and agar, which have demonstrated anticoagulant, antiviral, and anti-inflammatory activities [
52]. Brown algae (Ochrophyta, Phaeophyceae), on the other hand, are rich in unique polysaccharides called fucoidans, which have shown promising immunomodulatory and anticancer properties [
53].
Furthermore, algae have the ability to produce secondary metabolites as a response to environmental stresses such as light intensity, nutrient availability, temperature, and predation. These secondary metabolites serve various ecological functions, including defense mechanisms against pathogens and predators. Many of these compounds have exhibited bioactivity and therapeutic potential in the context of human health [
47].
The cultivation and harvesting of algae for the production of natural products have gained significant attention in recent years. Algae can be cultured in large-scale photobioreactors or open ponds, offering a sustainable and scalable source of bioactive compounds [
54]. Additionally, advances in algae biotechnology and genetic engineering have facilitated the optimization of algae strains to enhance the production of specific compounds of interest [
55].
Thus, algae represent a diverse and promising source of natural products with vast potential for various applications. Their photosynthetic capacity, genetic diversity, and ability to adapt to different environments contribute to the synthesis of a wide range of bioactive compounds [
56]. The exploration of algae as a source of natural products opens up avenues for the discovery of novel therapeutic agents, including those with potential applications in diabetes and its complications. Understanding the diversity and biosynthetic capabilities of algae is crucial for harnessing their potential and advancing the field of natural product research [
57].
2.2. Bioactive Compounds Present in Algae with Potential Antidiabetic Properties
Algae, with their remarkable chemical diversity, have been found to contain numerous bioactive compounds with potential antidiabetic properties. These compounds offer a rich source of natural products that can be explored for the development of novel therapeutic interventions in diabetes management. Here, we highlight some of the bioactive compounds present in algae that have shown promise in modulating key pathways involved in glucose homeostasis and diabetes-related complications [
13,
34].
2.2.1. Polysaccharides
Algae are known to produce a variety of polysaccharides with potential antidiabetic effects. For example, sulfated polysaccharides derived from red algae, such as carrageenan and agar, have demonstrated antihyperglycemic activity by inhibiting α-glucosidase and α-amylase enzymes involved in carbohydrate digestion, thereby reducing postprandial glucose levels. Additionally, these polysaccharides possess antioxidant properties and can enhance insulin sensitivity [
58,
59].
2.2.2. Polyphenols
Algae-derived polyphenols, including flavonoids and phenolic acids, have attracted attention for their potential antidiabetic effects. These compounds exhibit antioxidant and anti-inflammatory properties, which can help mitigate oxidative stress and chronic inflammation associated with diabetes. Some brown algae-derived polyphenols, such as phlorotannins, have shown inhibitory effects on α-glucosidase and α-amylase enzymes, leading to reduced glucose absorption and improved glycemic control [
60,
61].
2.2.3. Pigments
Algae are rich in pigments such as chlorophylls, carotenoids, and phycobiliproteins, which possess diverse biological activities. Fucoxanthin, a carotenoid found in brown algae, has shown promise in diabetes management by stimulating glucose uptake in skeletal muscle cells and adipocytes, improving insulin sensitivity. Moreover, certain algae-derived pigments possess antioxidant and anti-inflammatory properties, contributing to their potential role in mitigating diabetes-related complications [
33,
62].
2.2.4. Lipids
Algae-derived lipids, particularly omega-3 fatty acids such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), have been extensively studied for their beneficial effects in diabetes. These fatty acids have demonstrated antihyperglycemic, anti-inflammatory, and insulin-sensitizing properties [
63]. Additionally, lipids derived from microalgae, such as Chlorella and Spirulina, have shown potential in improving lipid profiles and reducing triglyceride levels in individuals with diabetes [
64].
2.2.5. Peptides and Proteins
Algae produce a wide range of peptides and proteins with various biological activities, including antidiabetic effects. Some algae-derived peptides have demonstrated inhibitory effects on dipeptidyl peptidase-4 (DPP-4), an enzyme involved in the degradation of incretin hormones. By inhibiting DPP-4, these peptides can prolong the action of incretins, leading to enhanced insulin secretion and improved glucose control [
65].
These are just a few examples of the bioactive compounds present in algae that hold promise for diabetes management. The multifaceted pharmacological activities of these compounds, including their ability to modulate glucose metabolism, enhance insulin sensitivity, and mitigate diabetes-related complications, make them attractive candidates for further exploration and development. Continued research into the bioactive compounds derived from algae will contribute to the discovery of novel therapeutic agents for effective diabetes management and improved patient outcomes [
33,
66].
2.3. Mechanisms of Action of Algae-Derived Natural Products in Diabetes Management
Algae-derived natural products exhibit diverse mechanisms of action that contribute to their potential in diabetes management. These bioactive compounds target key pathways involved in glucose homeostasis, insulin sensitivity, and the prevention or mitigation of diabetes-related complications. Understanding the mechanisms underlying the actions of algae-derived natural products is essential for harnessing their therapeutic potential. Here, we discuss some of the mechanisms by which these compounds exert their effects in diabetes management [
33,
67].
2.3.1. Regulation of Glucose Metabolism
Algae-derived natural products have been found to modulate enzymes involved in glucose metabolism, such as α-glucosidase and α-amylase. By inhibiting these enzymes, algae-derived compounds can slow down the breakdown and absorption of carbohydrates, leading to reduced postprandial glucose levels. This effect is particularly important in managing blood glucose fluctuations after meals [
33,
68].
2.3.2. Enhancement of Insulin Sensitivity
Insulin resistance, a hallmark of type 2 diabetes, is characterized by impaired response to insulin and reduced glucose uptake by cells. Algae-derived natural products have shown potential in improving insulin sensitivity. They can activate signaling pathways involved in insulin action, such as the PI3K/Akt pathway, promoting glucose uptake and utilization by cells. By enhancing insulin sensitivity, these compounds contribute to better glycemic control and metabolic regulation [
69,
70].
2.3.3. Antioxidant and Anti-Inflammatory Activities
Chronic hyperglycemia in diabetes leads to the production of reactive oxygen species (ROS) and the activation of inflammatory pathways, contributing to oxidative stress and chronic inflammation. Algae-derived natural products possess antioxidant and anti-inflammatory properties, effectively neutralizing ROS and reducing inflammatory responses. This antioxidant and anti-inflammatory activity can help mitigate the cellular damage and tissue dysfunction associated with diabetes [
71].
2.3.4. Modulation of Adipokine Secretion
Adipokines are signaling molecules secreted by adipose tissue that play a crucial role in glucose and lipid metabolism. Algae-derived natural products have been shown to influence adipokine secretion, including adiponectin and leptin. Adiponectin, an insulin-sensitizing hormone, promotes glucose utilization and enhances insulin sensitivity [
72]. Algae-derived compounds can increase adiponectin levels, thereby improving insulin action and glucose metabolism. Conversely, modulation of leptin levels by algae-derived compounds may help regulate appetite and body weight, which are important factors in diabetes management [
73].
2.3.5. Prevention of Diabetes-Related Complications
Algae-derived natural products have demonstrated potential in mitigating diabetes-related complications such as diabetic retinopathy and nephropathy. These compounds possess antiangiogenic and anti-inflammatory properties, which can protect retinal cells and prevent the development or progression of retinopathy [
74]. Additionally, algae-derived compounds have shown reno-protective effects by reducing albuminuria, attenuating renal fibrosis, and modulating inflammatory pathways. These effects contribute to the preservation of renal function in individuals with diabetes [
75].
The multifaceted mechanisms of action exhibited by algae-derived natural products make them promising candidates for diabetes management. Their ability to modulate glucose metabolism, enhance insulin sensitivity, exert antioxidant and anti-inflammatory effects, and prevent complications highlights their potential therapeutic value. Continued research into the mechanisms underlying the actions of algae-derived compounds will facilitate the development of targeted interventions for effective diabetes management and improved patient outcomes [
33,
34].
3. Algae-Derived Natural Products in Glycemic Control
3.1. Exploration of Algae-Derived Compounds in Regulating Blood Glucose Levels
Algae-derived natural products have shown promise in regulating blood glucose levels and improving glycemic control. These compounds possess diverse mechanisms of action that contribute to their potential as antidiabetic agents. Here, we explore the role of algae-derived compounds in glycemic control and their potential applications in diabetes management [
13,
33].
3.1.1. Inhibition of Carbohydrate-Digesting Enzymes
Algae-derived compounds have been found to inhibit enzymes involved in the digestion and absorption of carbohydrates, such as α-glucosidase and α-amylase. By inhibiting these enzymes, algae-derived compounds can delay the breakdown of complex carbohydrates into glucose and reduce the rate of glucose absorption from the intestine. This results in a slower and more controlled release of glucose into the bloodstream, preventing postprandial hyperglycemia [
44,
68].
3.1.2. Stimulation of Glucose Uptake
Algae-derived natural products have demonstrated the ability to enhance glucose uptake by cells, particularly in skeletal muscle and adipose tissue. These compounds can activate signaling pathways, such as the PI3K/Akt pathway, which are involved in insulin-mediated glucose uptake. By promoting glucose uptake, algae-derived compounds help to lower blood glucose levels and improve insulin sensitivity [
44,
76].
3.1.3. Modulation of Insulin Secretion
Algae-derived compounds have been found to influence insulin secretion from pancreatic β-cells. Some compounds have shown the ability to enhance insulin secretion in response to elevated glucose levels, helping to maintain proper glucose homeostasis. This effect is particularly beneficial in individuals with impaired insulin secretion, such as those with type 2 diabetes [
33,
44].
3.1.4. Regulation of Hepatic Glucose Production
The liver plays a crucial role in maintaining glucose balance by producing and releasing glucose into the bloodstream. Algae-derived compounds have been shown to regulate hepatic glucose production by modulating key enzymes involved in gluconeogenesis and glycogenolysis [
77]. By inhibiting these enzymes, algae-derived compounds can reduce excessive glucose production by the liver and contribute to improved glycemic control [
13,
33].
3.1.5. Anti-Inflammatory and Antioxidant Effects
Chronic inflammation and oxidative stress are closely associated with insulin resistance and impaired glucose metabolism. Algae-derived compounds possess anti-inflammatory and antioxidant properties, which can help mitigate these underlying factors in diabetes. By reducing inflammation and oxidative stress, these compounds contribute to improved glycemic control and overall metabolic health [
78].
The exploration of algae-derived compounds in regulating blood glucose levels holds promise for the development of novel therapeutic interventions in diabetes management. These compounds offer unique mechanisms of action that complement existing antidiabetic therapies and may help address the limitations of current treatment approaches [
33]. Continued research and optimization of algae-derived compounds will contribute to their potential application as adjunctive therapies or as lead compounds for the development of new antidiabetic agents. Harnessing the glycemic-regulating properties of algae-derived natural products has the potential to improve glycemic control, enhance insulin sensitivity, and ultimately improve the quality of life for individuals living with diabetes [
79].
3.2. Evaluation of the Effects of Algae Extracts on Insulin Secretion and Sensitivity
The effects of algae extract on insulin secretion and sensitivity have been the subject of extensive investigation, shedding light on their potential in glycemic control and diabetes management. Algae-derived natural products offer a diverse array of bioactive compounds that have demonstrated promising effects in modulating insulin secretion and enhancing insulin sensitivity. Here, we evaluate the effects of algae extracts on insulin-related parameters and their implications for glycemic control [
13,
33].
3.2.1. Insulin Secretion
Algae extracts have been found to influence insulin secretion from pancreatic β-cells. Studies have shown that certain algae-derived compounds can stimulate insulin secretion in response to glucose stimulation. These compounds act through various mechanisms, including the closure of ATP-sensitive potassium channels and the subsequent influx of calcium ions, leading to the release of insulin vesicles. By promoting insulin secretion, algae extracts can help regulate blood glucose levels and maintain glucose homeostasis [
13,
33].
3.2.2. Insulin Sensitivity
Insulin resistance, characterized by reduced responsiveness of target tissues to insulin, is a key feature of type 2 diabetes. Algae extracts have demonstrated the ability to enhance insulin sensitivity in different cell types and animal models. These extracts can activate intracellular signaling pathways, such as the PI3K/Akt pathway, which play a critical role in insulin-mediated glucose uptake. By improving insulin sensitivity, algae extracts facilitate the efficient utilization of glucose by cells and contribute to better glycemic control [
80].
3.2.3. Adipocyte Function
Adipose tissue is an important regulator of insulin sensitivity and glucose metabolism. Algae extracts have been shown to modulate adipocyte function, influencing adipokine secretion and adipocyte differentiation. Adipokines, such as adiponectin, play a crucial role in glucose and lipid metabolism. Algae extracts can increase adiponectin secretion, which enhances insulin sensitivity and improves glucose uptake by cells. Additionally, algae extracts have been found to inhibit adipocyte hypertrophy and promote the browning of white adipose tissue, further contributing to metabolic improvements [
73,
81].
3.2.4. Mitochondrial Function
Impaired mitochondrial function has been implicated in insulin resistance and glucose intolerance. Algae extracts have demonstrated the ability to improve mitochondrial function, enhancing cellular energy metabolism and insulin sensitivity. These extracts can promote mitochondrial biogenesis, increase mitochondrial respiration, and enhance ATP production. By improving mitochondrial function, algae extracts optimize cellular energy utilization and promote glucose uptake and metabolism [
82].
3.2.5. Inflammatory and Oxidative Stress Modulation
Chronic inflammation and oxidative stress contribute to insulin resistance and impaired glucose metabolism. Algae extracts possess anti-inflammatory and antioxidant properties, which can attenuate inflammation and reduce oxidative stress in insulin-responsive tissues. By mitigating these underlying factors, algae extracts improve insulin sensitivity and promote better glycemic control [
83].
The evaluation of algae extracts on insulin secretion and sensitivity provides valuable insights into their potential therapeutic applications in glycemic control and diabetes management. These extracts offer a multitude of bioactive compounds that target key pathways involved in insulin regulation and glucose metabolism. Continued research is needed to unravel the specific mechanisms of action of algae extracts and identify the active components responsible for their effects. Harnessing the potential of algae-derived natural products in improving insulin secretion and sensitivity holds great promise for the development of novel therapeutic interventions for diabetes [
84].
3.3. Algae-Based Natural Products as Inhibitors of Carbohydrate-Digesting Enzymes
Algae-based natural products have shown promising inhibitory effects on carbohydrate-digesting enzymes, making them potential candidates for glycemic control and the management of diabetes. Carbohydrate-digesting enzymes, such as α-glucosidase and α-amylase, play a critical role in the breakdown of complex carbohydrates into glucose. Inhibition of these enzymes can help regulate postprandial blood glucose levels and prevent glucose spikes. Here, we explore the inhibitory effects of algae-based natural products on carbohydrate-digesting enzymes and their implications for glycemic control [
85,
86].
3.3.1. α-. Glucosidase Inhibition
Algae-based natural products have been found to inhibit α-glucosidase, an enzyme responsible for the final step in the breakdown of complex carbohydrates into glucose. By inhibiting α-glucosidase, algae-based compounds delay the digestion and absorption of carbohydrates, leading to a slower release of glucose into the bloodstream. This inhibition helps prevent rapid glucose spikes after meals and contributes to better glycemic control [
68,
85].
3.3.2. α-. Amylase Inhibition
Algae-based natural products have also demonstrated inhibitory effects on α-amylase, an enzyme that initiates the digestion of starch into smaller carbohydrate units. Inhibition of α-amylase by algae-based compounds slows down the breakdown of starch, reducing the rate at which glucose is released into the bloodstream. By inhibiting α-amylase, algae-based natural products can help regulate postprandial blood glucose levels and prevent excessive glucose fluctuations [
87,
88].
3.3.3. Mechanisms of Inhibition
The inhibitory effects of algae-based (for example from
Halimeda tuna, Chlorophyta,
Figure 1) natural products on carbohydrate-digesting enzymes are attributed to their bioactive components, such as polyphenols, flavonoids, and polysaccharides. These compounds interact with the active sites of α-glucosidase and α-amylase, preventing their enzymatic activity and substrate binding. This inhibition leads to reduced carbohydrate breakdown and glucose absorption, resulting in improved glycemic control [
89,
90].
3.3.4. Synergistic Effects
Algae-based natural products often contain a complex mixture of bioactive compounds that can act synergistically to enhance their inhibitory effects on carbohydrate-digesting enzymes. The combined action of multiple compounds may result in more potent enzyme inhibition and better glycemic control. Additionally, the presence of other bioactive components in algae-based natural products, such as antioxidants and anti-inflammatory compounds, can provide additional health benefits and contribute to overall metabolic improvements [
32,
33].
3.3.5. Therapeutic Potential
The inhibition of carbohydrate-digesting enzymes by algae-based (for example from
Ascophyllum nodosum, Fucus vesiculosus and
Undaria pinnatifida, Phaeophyceae,
Figure 2) natural products presents an attractive therapeutic approach for glycemic control and diabetes management. By slowing down carbohydrate digestion and reducing glucose absorption, these natural products offer a natural and potentially safer alternative to synthetic enzyme inhibitors. Furthermore, the use of algae-based natural products as enzyme inhibitors aligns with the growing interest in plant-based therapies and the development of functional foods or dietary supplements for diabetes management [
13,
68].
The exploration of algae-based (for example,
Dictyopteris polypodioides, Phaeophyceae,
Figure 3) natural products as inhibitors of carbohydrate-digesting enzymes highlights their potential in glycemic control and diabetes management. The inhibitory effects of these natural products on α-glucosidase and α-amylase contribute to the regulation of postprandial blood glucose levels and the prevention of glucose spikes [
91]. Further research is needed to identify the active compounds responsible for these inhibitory effects and to evaluate their safety and efficacy in clinical settings. Incorporating algae-based natural products as enzyme inhibitors may offer a novel and natural approach to support glycemic control in individuals with diabetes.
4. Algae-Derived Natural Products in Diabetic Complications
4.1. Role of Algae-Derived Compounds in Preventing and Managing Diabetic Retinopathy
Algae-derived (for example from
Alaria, Palmaria and
Ulva,
Figure 4) natural products have shown potential in preventing and managing diabetic retinopathy, a common complication of diabetes that affects the eyes [
92]. Diabetic retinopathy is characterized by damage to the blood vessels in the retina, leading to vision impairment and, in severe cases, blindness. Here, we explore the role of algae-derived compounds in preventing and managing diabetic retinopathy and their underlying mechanisms of action [
35].
4.1.1. Anti-Angiogenic Effects
Diabetic retinopathy is associated with abnormal blood vessel growth in the retina, a process known as angiogenesis [
93]. Algae-derived compounds have demonstrated anti-angiogenic properties by inhibiting the proliferation and migration of endothelial cells, which are essential for blood vessel formation. These compounds target various signaling pathways involved in angiogenesis, such as vascular endothelial growth factor (VEGF) signaling, to suppress abnormal blood vessel growth and reduce the risk of diabetic retinopathy progression [
94].
4.1.2. Antioxidant and Anti-Inflammatory Properties
Oxidative stress and chronic inflammation play significant roles in the development and progression of diabetic retinopathy [
95]. Algae-derived compounds possess antioxidant and anti-inflammatory properties, which help mitigate these damaging processes. These compounds scavenge reactive oxygen species, reduce oxidative stress, and suppress inflammatory signaling pathways. By alleviating oxidative stress and inflammation, algae-derived compounds protect retinal cells from damage and promote retinal health [
83].
4.1.3. Neuroprotective Effects
Diabetic retinopathy involves not only vascular changes but also neuronal damage in the retina. Algae-derived (for example, Acetabularia acetabulum, Chlorophyta,
Figure 5) compounds have shown neuroprotective effects by preserving retinal ganglion cells, photoreceptor cells, and other retinal neurons. These compounds can enhance neuronal survival, promote neurite outgrowth, and modulate neurotrophic factors. By protecting retinal neurons, algae-derived compounds contribute to the prevention and management of diabetic retinopathy-related vision loss [
96,
97].
4.1.4. Modulation of Retinal Blood Flow
Algae-derived (for example,
Dunaliella salina, Chlorophyta,
Figure 6) compounds have the potential to modulate retinal blood flow, which is often compromised in diabetic retinopathy. These compounds can improve blood circulation, enhance microvascular perfusion, and regulate endothelial function. By optimizing retinal blood flow, algae-derived compounds support proper oxygen and nutrient supply to retinal cells, reducing the risk of ischemia and further damage [
98].
4.1.5. Restoration of Retinal Barrier Function
Disruption of the blood-retinal barrier is a hallmark of diabetic retinopathy, leading to increased vascular permeability and fluid leakage [
99]. Algae-derived compounds have shown the ability to restore the integrity of the blood-retinal barrier by regulating tight junction proteins and reducing endothelial permeability. By preserving the barrier function, these compounds prevent the accumulation of fluid in the retina and inhibit the progression of diabetic retinopathy [
100].
The role of algae-derived compounds in preventing and managing diabetic retinopathy is promising and offers new possibilities for therapeutic interventions. Their anti-angiogenic, antioxidant, anti-inflammatory, neuroprotective, and vascular modulatory effects contribute to the overall preservation of retinal health [
101]. Further research is needed to identify specific algae-derived compounds and elucidate their mechanisms of action in diabetic retinopathy. Harnessing the potential of algae-derived natural products may provide novel approaches for preventing and managing diabetic retinopathy, ultimately improving visual outcomes and quality of life for individuals with diabetes [
102].
4.2. Algae-Based Interventions for Diabetic Nephropathy and Its Associated Complications
Algae-derived natural products, particularly those derived from specific algae species (for example,
Fucus spiralis and
Taonia atomaria, Phaeophyceae,
Figure 7), hold promise as interventions for diabetic nephropathy and its associated complications [
13,
33]. Diabetic nephropathy, a progressive kidney disease caused by diabetes, is characterized by kidney damage and impaired renal function. Here, we explore the potential of algae-based interventions, focusing on specific algae species, in preventing and managing diabetic nephropathy and its associated complications.
4.2.1. Reno-Protective Effects
Studies have shown that extracts from the brown macroalga species
Fucus vesiculosus possess reno-protective effects by preserving renal function and attenuating kidney damage. The antioxidant and anti-inflammatory properties of
F. vesiculosus extracts help mitigate oxidative stress and inflammation in the kidneys, key contributors to diabetic nephropathy [
103].
4.2.2. Anti-Fibrotic Properties
Extracts from the macroalga species
Gracilariopsis lemaneiformis (formerly
Gracilaria lemaneiformis) (Rhodophyta) have demonstrated anti-fibrotic effects in diabetic nephropathy models. These extracts inhibit the production and deposition of collagen and other fibrotic markers in the kidneys, thereby preventing the progression of renal fibrosis and preserving renal function [
104].
4.2.3. Blood Pressure Regulation
The green microalga species
Chlorella vulgaris has been investigated for its blood pressure-regulating effects [
105].
C. vulgaris supplementation has shown promising results in regulating blood pressure levels by modulating vasoactive factors and improving endothelial function [
106].
4.2.4. Glycemic Control
Extracts from the Cyanobacteria
Arthrospira platensis (formerly
Spirulina platensis) have been shown to regulate blood glucose levels and improve insulin sensitivity [
107]. A. platensis supplementation contributes to better glycemic control, reducing the burden on the kidneys and minimizing the risk of renal complications [
108].
4.2.5. Mineral and Electrolyte Balance
The brown macroalga species
Ecklonia cava has been investigated for its ability to maintain proper mineral and electrolyte balance. E. cava extracts have been shown to regulate serum levels of potassium, sodium, calcium, and phosphate, supporting renal homeostasis and preventing complications associated with electrolyte imbalances [
109].
4.2.6. Anti-Inflammatory and Antioxidant Effects
Extracts from the green microalga species
Dunaliella salina possess anti-inflammatory and antioxidant properties. These extracts help reduce inflammation and oxidative stress in the kidneys, alleviating renal damage and promoting renal health [
110].
The use of specific algae species, such as
Fucus vesiculosus, Pyropia yezoensis (
Figure 8)
, Chlorella vulgaris, Arthrospira platensis, Ecklonia cava, and
Dunaliella salina, in diabetic nephropathy research offers targeted therapeutic strategies [
13,
33,
102,
103,
104,
105,
106,
107,
108,
109,
110]. Their reno-protective, anti-fibrotic, blood pressure-regulating, glycemic control, mineral and electrolyte balancing, anti-inflammatory, and antioxidant effects collectively contribute to the prevention and management of diabetic nephropathy. Further research is needed to explore the full potential of these algae species and their derived compounds in clinical settings. Incorporating algae-based interventions from specific species may provide novel therapeutic options for individuals with diabetic nephropathy, aiming to slow disease progression, preserve renal function, and improve overall patient outcomes [
111].
4.3. Algae-Derived Natural Products as Potential Therapeutics for Diabetic Neuropathy
Algae-derived natural products have shown potential as potential therapeutics for diabetic neuropathy, a common complication of diabetes characterized by nerve damage and dysfunction. The diverse chemical constituents of various algae species offer a rich source of bioactive compounds with neuroprotective properties. Here, we explore the potential of specific algae species and their derived natural products in the management of diabetic neuropathy [
112].
Extracts from the brown macroalga
Ecklonia cava have demonstrated neuroprotective effects in diabetic neuropathy models. These extracts contain phlorotannins, a class of polyphenols known for their antioxidant and anti-inflammatory properties. E. cava extracts have been shown to protect nerve cells from oxidative stress, reduce inflammation, and improve nerve function in diabetic neuropathy [
111,
113].
The green macroalga
Ulva lactuca has been investigated for its potential neuroprotective effects.
U. lactuca extracts contain bioactive compounds such as ulvan, which exhibits antioxidant and anti-inflammatory activities. These extracts have shown promise in reducing nerve damage and improving nerve conduction velocity in diabetic neuropathy models [
114].
Extracts from the red seaweed
Gracilaria edulis have been studied for their potential in diabetic neuropathy management.
G. edulis extracts contain sulfated polysaccharides, which possess antioxidant and anti-inflammatory properties. These extracts have shown promising effects in protecting nerve cells, improving nerve conduction, and reducing neuropathic pain in diabetic neuropathy models [
115].
The brown algae genus Sargassum has been investigated for its potential in diabetic neuropathy. Sargassum spp. extracts contain various bioactive compounds such as fucoidan, fucoxanthin, and phlorotannins, which exhibit antioxidant, anti-inflammatory, and neuroprotective activities. These extracts have shown potential in protecting nerve cells and improving nerve function in diabetic neuropathy models [
116].
Extracts from the red macroalga
Gelidium elegans have been studied for their neuroprotective effects in diabetic neuropathy.
G. elegans extracts contain bioactive compounds such as agarobiose and agar-oligosaccharides, which possess antioxidant and anti-inflammatory properties. These extracts have shown potential in improving nerve function and reducing neuropathic pain in diabetic neuropathy models [
117].
The use of specific algae species, including
Ecklonia cava, Ulva lactuca, Gracilaria edulis, Sargassum spp., and
Gelidium elegans, offers exciting prospects for the development of natural therapeutics for diabetic neuropathy. Their neuroprotective, antioxidant, and anti-inflammatory properties contribute to the preservation of nerve health and function [
118]. Further research is needed to explore the specific mechanisms of action and identify key bioactive compounds within these algae species. Incorporating algae-derived natural products may provide novel therapeutic options for individuals with diabetic neuropathy, aiming to alleviate symptoms, improve nerve function, and enhance the quality of life [
32].
5. Mechanistic Insights and Molecular Targets
5.1. Elucidating the Molecular Mechanisms Underlying the Antidiabetic Effects of Algae-Derived Compounds
Elucidating the molecular mechanisms underlying the antidiabetic effects of algae-derived compounds is crucial for understanding their therapeutic potential. Extensive research has been conducted to unravel the intricate pathways and molecular targets involved. Here, we provide an overview of the current understanding of the mechanisms of action of algae-derived compounds in diabetes management, shedding light on their molecular targets [
119].
5.1.1. AMP-Activated Protein Kinase (AMPK) Activation
AMPK is a key regulator of energy metabolism and glucose homeostasis. Several algae-derived compounds, such as fucoidan from the brown macroalga
F. vesiculosus [
120], and phycocyanin from the blue-green microalga
Arthrospira platensis [
121], have been found to activate AMPK. Activation of AMPK leads to increased glucose uptake, enhanced insulin sensitivity, and improved glycemic control.
5.1.2. Peroxisome Proliferator-Activated Receptor Gamma (PPARγ) Modulation
PPARγ is a nuclear receptor involved in insulin sensitivity and glucose metabolism. Some algae-derived compounds, such as fucoxanthin from brown algae [
122] and ulvan from de green macroalga
Ulva lactuca [
32], have been shown to modulate PPARγ activity. Activation of PPARγ by these compounds can improve insulin sensitivity, promote adipocyte differentiation, and regulate lipid metabolism [
122].
5.1.3. Inhibition of Carbohydrate-Digesting Enzymes
Algae-derived compounds, including sulfated polysaccharides from the red macroalga
Gracilaria edulis [
13] and fucoidan from brown algae (
F. vesiculosus and
A. nodosum) [
124], have demonstrated inhibitory effects on carbohydrate-digesting enzymes such as α-amylase and α-glucosidase. By inhibiting these enzymes, algae-derived compounds can reduce postprandial glucose levels and attenuate hyperglycemia.
5.1.4. Antioxidant and Anti-Inflammatory Effects
Oxidative stress and chronic inflammation play crucial roles in the development and progression of diabetes. Algae-derived compounds, such as phlorotannins from
Ecklonia cava [
125], and sulfated polysaccharides from
Pyropia tenera (formerly
Porphyra tenera) (
Figure 9) [
126], exhibit potent antioxidant and anti-inflammatory activities. These compounds can mitigate oxidative stress, suppress inflammatory pathways, and protect pancreatic beta cells from damage.
5.1.5. Modulation of Insulin Signaling Pathway
Algae-derived compounds have been found to modulate various components of the insulin signaling pathway. For instance, Phycocyanin from
Arthrospira maxima and
A. platensis have been shown to increase insulin receptor substrate 1 (IRS-1) phosphorylation and activate downstream signaling cascades [
33,
127]. These compounds can improve insulin signaling, promote glucose uptake, and regulate insulin secretion.
5.2. Identification of Key Molecular Targets Influenced by Algae-Derived Natural Products
Identification of key molecular targets influenced by algae-derived natural products is crucial for understanding their mechanisms of action in diabetes management. Extensive research has been conducted to unravel the intricate pathways and molecular targets involved. Here, we provide an overview of the current understanding of the molecular targets influenced by algae-derived (for example,
Ulva reticulata, Chlorophyta) compounds and their implications in antidiabetic effects [
128].
5.2.1. Peroxisome Proliferator-Activated Receptor Gamma (PPARγ)
PPARγ is a nuclear receptor involved in insulin sensitivity and glucose metabolism. Several algae-derived compounds, such as fucoxanthin from brown algae [
130], and ulvan from
Ulva lactuca [
130], have been shown to modulate PPARγ activity. Activation of PPARγ improves insulin sensitivity, promotes adipocyte differentiation, and regulates lipid metabolism.
5.2.2. AMP-Activated Protein Kinase (AMPK)
AMPK is a key regulator of energy metabolism and glucose homeostasis. Algae-derived compounds, including fucoidan from
F. vesiculosus [
131] and phycocyanin from A. platensis [
127], have been found to activate AMPK. Activation of AMPK leads to increased glucose uptake, enhanced insulin sensitivity, and improved glycemic control.
5.2.3. Protein Tyrosine Phosphatase 1B (PTP1B)
PTP1B is a negative regulator of insulin signaling and a therapeutic target for diabetes. Algae-derived compounds, such as phlorotannins from
Ecklonia cava [
132], and sulfated polysaccharide (porphyran) from
Pyropia yezoensis [
133], have been shown to inhibit PTP1B activity. Inhibition of PTP1B improves insulin signaling and glucose metabolism.
5.2.4. Nuclear Factor-Kappa B (NF-κB)
NF-κB is a transcription factor involved in inflammation and insulin resistance. Algae-derived compounds, including phlorotannins from
Ecklonia cava [
134], and fucoidan from brown algae (for example,
Sargassum siliquastrum) [
135], have demonstrated anti-inflammatory effects by suppressing NF-κB activation. Inhibition of NF-κB signaling pathway alleviates inflammation and improves insulin sensitivity.
5.2.5. Alpha-Glucosidase and Alpha-Amylase
Algae-derived compounds, such as sulfated polysaccharides from
G. edulis, and fucoidan from brown algae, have shown inhibitory effects on carbohydrate-digesting enzymes, including alpha-glucosidase and alpha-amylase. Inhibition of these enzymes reduces postprandial glucose levels and attenuates hyperglycemia [
32].
Understanding the molecular targets influenced by algae-derived natural products provides insights into their mechanisms of action in diabetes management. By targeting key molecular pathways, such as PPARγ, AMPK, PTP1B, NF-κB, and carbohydrate-digesting enzymes, algae-derived compounds exhibit promising antidiabetic effects. Further research is needed to elucidate the specific molecular mechanisms and interactions between these compounds and their molecular targets [
32,
67].
6. Challenges and Future Directions
6.1. Current Limitations and Challenges in Utilizing Algae-Derived Natural Products for Diabetes Management
Despite the promising potential of algae-derived natural products in diabetes management, several limitations and challenges need to be addressed for their successful utilization. Understanding these challenges and finding suitable solutions is crucial for the future development and application of algae-based interventions. Here, we discuss the current limitations and propose potential strategies for overcoming these challenges [
13,
33].
6.1.1. Standardization and Quality Control
One of the major challenges in utilizing algae-derived natural products is the lack of standardized extraction methods and quality control measures. Variations in algae species, growth conditions, harvesting methods, and extraction procedures can significantly impact the composition and bioactivity of the extracted compounds. Establishing standardized protocols for algae cultivation, extraction, and quality control is essential to ensure consistent and reproducible results [
54,
136].
6.1.2. Bioavailability and Pharmacokinetics
The bioavailability and pharmacokinetic profiles of algae-derived compounds are critical factors influencing their therapeutic efficacy. Some bioactive compounds may exhibit poor solubility, limited absorption, or rapid metabolism, leading to reduced bioavailability and efficacy. Strategies such as nanoencapsulation, formulation optimization, and prodrug approaches can be explored to enhance the bioavailability and pharmacokinetic properties of algae-derived compounds [
137,
138].
6.1.3. Safety and Toxicity Assessment
While algae-derived natural products are generally considered safe, comprehensive safety evaluations are essential to determine potential adverse effects and establish appropriate dosage guidelines [
139]. Toxicity studies, including acute and chronic toxicity assessments, should be conducted to ensure the safety of algae-based interventions [
140]. Furthermore, long-term studies are needed to evaluate the potential for accumulation of algae-derived compounds in tissues or organs [
31].
6.1.4. Translation to Clinical Applications
Although preclinical studies have shown promising results, the translation of algae-derived natural products to clinical applications faces several challenges. Rigorous clinical trials are necessary to validate the efficacy, safety, and optimal dosage regimens of algae-based interventions. Additionally, cost-effectiveness analyses and regulatory considerations should be considered for successful integration into clinical practice [
141].
6.1.5. Sustainability and Scalability
The sustainable production and scalability of algae-derived natural products are important considerations. Algae cultivation methods that minimize resource consumption, optimize productivity, and reduce environmental impact need to be developed. Additionally, the establishment of large-scale cultivation facilities and extraction technologies is crucial for meeting the increasing demand for algae-based interventions [
54].
Addressing these challenges requires interdisciplinary collaborations among researchers, industry partners, regulatory agencies, and healthcare providers. Overcoming these limitations and finding solutions will pave the way for the successful utilization of algae-derived natural products in diabetes management, ultimately benefiting patients worldwide [
142].
6.2. Strategies to Optimize the Therapeutic Potential of Algae-Based Interventions
To optimize the therapeutic potential of algae-based interventions in diabetes management, several strategies can be employed. Addressing the challenges and implementing these strategies will contribute to the development of effective algae-based therapeutics. Here, we discuss potential approaches to optimize the therapeutic potential of algae-based interventions and improve their efficacy [
33,
143].
6.2.1. Standardization and Quality Control
Standardizing algae cultivation, harvesting, and extraction methods is crucial for ensuring consistent composition and bioactivity of algae-derived natural products [
144]. Implementing quality control measures, such as standard operating procedures and rigorous testing, will enhance the reproducibility and reliability of algae-based interventions [
145].
6.2.2. Formulation Optimization
Developing appropriate formulations can improve the stability, solubility, and bioavailability of algae-derived compounds. Encapsulation techniques, such as nanoencapsulation or microencapsulation, can protect sensitive compounds, improve their delivery, and enhance their therapeutic efficacy [
146]. Formulation optimization also enables controlled release and targeted delivery of bioactive compounds to specific tissues or organs [
147].
6.2.3. Combination Therapy
Exploring the synergistic effects of algae-derived compounds with existing antidiabetic drugs or natural products can lead to enhanced therapeutic outcomes. Combining algae-derived compounds with complementary mechanisms of action may potentiate their antidiabetic effects and improve overall glycemic control. Synergistic interactions can also help reduce drug dosage and minimize side effects [
13,
32].
6.2.4. Pharmacokinetic Enhancements
Enhancing the pharmacokinetic properties of algae-derived compounds can improve their bioavailability and therapeutic efficacy. Strategies such as prodrug design, chemical modification, or co-administration with absorption enhancers can enhance drug absorption, distribution, metabolism, and excretion [
148]. Pharmacokinetic enhancements ensure optimal drug levels in target tissues and prolong the duration of action [
149].
6.2.5. Personalized Medicine Approaches
Taking individual patient characteristics, such as genetics, lifestyle, and comorbidities, into account can optimize the efficacy of algae-based interventions. Personalized medicine approaches can help tailor treatment regimens, dosage adjustments, and treatment durations to maximize therapeutic outcomes and minimize adverse effects [
33,
150].
6.2.6. Translational Research and Clinical Trials
Conducting well-designed translational research studies and large-scale clinical trials is essential for validating the safety and efficacy of algae-based interventions. Robust clinical evidence will enable the integration of algae-derived therapeutics into standard clinical practice and regulatory frameworks. These strategies require collaborative efforts among researchers, healthcare professionals, regulatory bodies, and industry partners to overcome the challenges associated with algae-based interventions and ensure their successful translation into clinical applications.
6.3. Future Prospects and Opportunities for Further Research and Development
The field of algae-based interventions in diabetes management holds immense potential for future research and development. Several opportunities and future prospects can further advance the utilization of algae-derived natural products [
33,
151,
152]. Here, we highlight the potential areas for exploration and opportunities for further research.
6.3.1. Identification of Novel Bioactive Compounds
Despite significant progress, the full spectrum of bioactive compounds present in algae and their potential effects on diabetes and its complications is yet to be fully explored. Further investigation into unexplored algae species and their unique metabolites may unveil novel bioactive compounds with potent antidiabetic properties. Advanced analytical techniques, such as metabolomics and proteomics, can facilitate the identification and characterization of these compounds [
44,
56,
66].
6.3.2. Mechanistic Elucidation
Understanding the precise mechanisms of action underlying the antidiabetic effects of algae-derived compounds is crucial for their targeted development and optimization. Future studies should focus on elucidating the molecular pathways and cellular targets influenced by algae-derived natural products, shedding light on their therapeutic mechanisms. Advances in omics technologies and molecular biology tools can aid in unraveling the intricate mechanisms involved [
153,
154,
155].
6.3.3. Preclinical and Clinical Studies
Robust preclinical studies and well-designed clinical trials are essential for establishing the safety and efficacy of algae-based interventions [
156]. Future research should aim to conduct comprehensive preclinical investigations to validate the therapeutic potential of algae-derived compounds in relevant animal models of diabetes and its complications. Subsequently, well-controlled clinical trials involving diverse patient populations will provide valuable insights into the efficacy, optimal dosage, and long-term effects of algae-based interventions [
32,
36].
6.3.4. Combination Therapies and Synergistic Approaches
Exploring the potential synergistic effects of algae-derived compounds with existing antidiabetic medications or natural products can enhance therapeutic outcomes. Combinatorial approaches involving algae-derived compounds and conventional antidiabetic drugs may lead to improved glycemic control and reduced side effects [
157]. Further investigation into synergistic interactions and combination therapies holds promise for enhanced therapeutic efficacy [
158].
6.3.5. Sustainable Cultivation and Extraction
Developing sustainable and scalable methods for algae cultivation and extraction is crucial for large-scale production of algae-derived natural products. Future research should focus on optimizing cultivation techniques, exploring novel cultivation systems, and implementing eco-friendly extraction methods [
159,
160]. These advancements will ensure a stable and reliable supply of algae-derived compounds for clinical applications.
6.3.6. Formulation Development and Drug Delivery Systems
Designing innovative formulations and drug delivery systems can enhance the bioavailability, stability, and targeted delivery of algae-derived compounds. Nanotechnology-based approaches, such as nanoparticles, liposomes, or hydrogels, offer opportunities for controlled release and site-specific delivery of bioactive compounds [
161,
162]. Developing optimized formulations will maximize the therapeutic potential of algae-based interventions.
By addressing these future prospects and opportunities, further research and development in algae-based interventions for diabetes and its complications can lead to novel therapeutic strategies, improved patient outcomes, and a better understanding of the potential of natural products derived from algae.
7. Conclusions
Algae-derived natural products have emerged as promising candidates for the management of diabetes and its complications [
13,
33]. The diverse chemical constituents and multifaceted pharmacological activities of algae make them attractive sources of bioactive compounds with potential antidiabetic properties. Throughout this review article, we have highlighted the significance of natural products and their derivatives in diabetes management, specifically focusing on algae-derived compounds [
31,
163].
We discussed the importance of algae-derived natural products in diabetes research, emphasizing their unique potential in addressing the global burden of this disease. The exploration of algae as a source of natural products revealed a vast diversity of bioactive compounds, including polysaccharides, polyphenols, pigments, and peptides, which exhibit potential antidiabetic effects [
13,
33,
44]. Mechanistic insights into the therapeutic properties of algae-derived compounds have shed light on their ability to regulate blood glucose levels, enhance insulin secretion and sensitivity, and inhibit carbohydrate-digesting enzymes [
33,
154,
164]. Furthermore, algae-based interventions have shown promise in preventing and managing diabetic complications, such as retinopathy and nephropathy [
33,
36,
104,
111].
While significant progress has been made in understanding the potential of algae-derived natural products in diabetes management, there is still much to be explored. Continued research and exploration in this field are crucial to unraveling the full potential of algae and their bioactive compounds. Further investigation into unexplored algae species and their metabolites may lead to the discovery of novel bioactive compounds with enhanced antidiabetic properties [
66,
165].
Additionally, it is important to elucidate the molecular mechanisms underlying the antidiabetic effects of algae-derived compounds. Future studies should focus on identifying key molecular targets influenced by these compounds, as this knowledge will facilitate targeted development and optimization of algae-based interventions [
32,
33].
Furthermore, conducting robust preclinical studies and well-designed clinical trials will provide valuable evidence on the safety, efficacy, and optimal use of algae-derived interventions in diverse patient populations. Translating the promising preclinical findings into clinical practice requires rigorous evaluation and validation [
141,
166].
Collaborative efforts among researchers, healthcare professionals, regulatory bodies, and industry partners are essential to overcome the challenges associated with algae-based interventions and ensure their successful translation into clinical applications [
167]. Continued research and exploration in this field hold the potential to revolutionize diabetes management and improve patient outcomes.
Author Contributions
Conceptualization, L.P. and A.V.; writing—original draft preparation, L.P.; writing—review and editing, L.P. and A.V. All authors have read and agreed to the published version of the manuscript.
Funding
Leonel Pereira thanks to the Fundação para a Ciência e Tecnologia, I. P (FCT), under the projects UIDB/04292/2020, UIDP/04292/2020, granted to MARE, and LA/P/0069/2020, granted to the Associate Laboratory ARNET.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Not applicable.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Wu, Y.; Ding, Y.; Tanaka, Y.; Zhang, W. , Risk Factors Contributing to Type 2 Diabetes and Recent Advances in the Treatment and Prevention. International Journal of Medical Sciences 2014, 11, 1185–1200. [Google Scholar] [CrossRef]
- Tomic, D.; Shaw, J. E.; Magliano, D. J. , The burden and risks of emerging complications of diabetes mellitus. Nature Reviews Endocrinology 2022, 18, 525–539. [Google Scholar] [CrossRef] [PubMed]
- Galicia-Garcia, U.; Benito-Vicente, A.; Jebari, S.; Larrea-Sebal, A.; Siddiqi, H.; Uribe, K.B.; Ostolaza, H.; Martín, C. Pathophysiology of Type 2 Diabetes Mellitus. Int. J. Mol. Sci. 2020, 21, 6275. [Google Scholar] [CrossRef] [PubMed]
- Kyrou, I. , Tsigos, C., Mavrogianni, C. et al. Sociodemographic and lifestyle-related risk factors for identifying vulnerable groups for type 2 diabetes: a narrative review with emphasis on data from Europe. BMC Endocr. Disord. 2020, 20, 134. [Google Scholar] [CrossRef]
- Popoviciu, M.S.; Kaka, N.; Sethi, Y.; Patel, N.; Chopra, H.; Cavalu, S. Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine. J. Pers. Med. 2023, 13, 422. [Google Scholar] [CrossRef]
- Choudhury, A. A.; Devi Rajeswari, V. , Gestational diabetes mellitus - A metabolic and reproductive disorder. Biomed. & Pharmacother. 2021, 143, 112183. [Google Scholar] [CrossRef]
- Cade, W. T. , Diabetes-Related Microvascular and Macrovascular Diseases in the Physical Therapy Setting. Phys. Ther. 2008, 88, 1322–1335. [Google Scholar] [CrossRef]
- Chawla, A.; Chawla, R.; Jaggi, S. , Microvasular and macrovascular complications in diabetes mellitus: Distinct or continuum? Indian J. Endocrinol. Metab. 2016, 20, 546–551. [Google Scholar] [CrossRef]
- Li K, Ferguson T, Embil J, Rigatto C, Komenda P, Tangri N. Risk of Kidney Failure, Death, and Cardiovascular Events After Lower Limb Complications in Patients With CKD. Kidney Int. Rep. 2020, 6, 381–388. [Google Scholar] [CrossRef]
- Kosmalski, M.; Śliwińska, A.; Drzewoski, J. Non-Alcoholic Fatty Liver Disease or Type 2 Diabetes Mellitus—The Chicken or the Egg Dilemma. Biomedicines 2023, 11, 1097. [Google Scholar] [CrossRef]
- Williams DM, Jones H, Stephens JW. Personalized Type 2 Diabetes Management: An Update on Recent Advances and Recommendations. Diabetes Metab Syndr Obes. 2022, 15, 281–295. [Google Scholar] [CrossRef] [PubMed]
- Davies, M. J.; Aroda, V. R.; Collins, B. S.; Gabbay, R. A.; Green, J.; Maruthur, N. M.; Rosas, S. E.; Del Prato, S.; Mathieu, C.; Mingrone, G.; Rossing, P.; Tankova, T.; Tsapas, A.; Buse, J. B. Management of Hyperglycemia in Type 2 Diabetes, 2022. A Consensus Report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care 2022, 45, 2753–2786. [Google Scholar] [CrossRef] [PubMed]
- Abo-Shady, A.M.; Gheda, S.F.; Ismail, G.A.; Cotas, J.; Pereira, L.; Abdel-Karim, O.H. Antioxidant and Antidiabetic Activity of Algae. Life 2023, 13, 460. [Google Scholar] [CrossRef]
- Quitério, E.; Soares, C.; Ferraz, R.; Delerue-Matos, C.; Grosso, C. Marine Health-Promoting Compounds: Recent Trends for Their Characterization and Human Applications. Foods 2021, 10, 3100. [Google Scholar] [CrossRef] [PubMed]
- Salehi, B.; Ata, A.; V. Anil Kumar, N.; Sharopov, F.; Ramírez-Alarcón, K.; Ruiz-Ortega, A.; Abdulmajid Ayatollahi, S.; Valere Tsouh Fokou, P.; Kobarfard, F.; Amiruddin Zakaria, Z.; et al. Antidiabetic Potential of Medicinal Plants and Their Active Components. Biomolecules 2019, 9, 551. [Google Scholar] [CrossRef]
- Liu, Y.; Zeng, S.; Ji, W.; Yao, H.; Lin, L.; Cui, H.; Santos, H. A.; Pan, G. , Emerging Theranostic Nanomaterials in Diabetes and Its Complications. Adv. Sci. 2022, 9, 2102466. [Google Scholar] [CrossRef]
- Andreozzi, F.; Candido, R.; Corrao, S.; Fornengo, R.; Giancaterini, A.; Ponzani, P.; Ponziani, M. C.; Tuccinardi, F.; Mannino, D. , Clinical inertia is the enemy of therapeutic success in the management of diabetes and its complications: a narrative literature review. Diabetol. Metab. Syndr. 2020, 12, 52. [Google Scholar] [CrossRef]
- Tran, N.; Pham, B.; Le, L. Bioactive Compounds in Anti-Diabetic Plants: From Herbal Medicine to Modern Drug Discovery. Biology 2020, 9, 252. [Google Scholar] [CrossRef]
- Tsivileva, O.M.; Koftin, O.V.; Evseeva, N.V. Coumarins as Fungal Metabolites with Potential Medicinal Properties. Antibiotics 2022, 11, 1156. [Google Scholar] [CrossRef]
- Wink, M. Modes of Action of Herbal Medicines and Plant Secondary Metabolites. Medicines 2015, 2, 251–286. [Google Scholar] [CrossRef]
- Yeshi, K.; Crayn, D.; Ritmejerytė, E.; Wangchuk, P. Plant Secondary Metabolites Produced in Response to Abiotic Stresses Has Potential Application in Pharmaceutical Product Development. Molecules 2022, 27, 313. [Google Scholar] [CrossRef] [PubMed]
- Galicia-Garcia, U.; Benito-Vicente, A.; Jebari, S.; Larrea-Sebal, A.; Siddiqi, H.; Uribe, K.B.; Ostolaza, H.; Martín, C. Pathophysiology of Type 2 Diabetes Mellitus. Int. J. Mol. Sci. 2020, 21, 6275. [Google Scholar] [CrossRef] [PubMed]
- Merabet, N.; Lucassen, P. J.; Crielaard, L.; Stronks, K.; Quax, R.; Sloot, P. M. A.; la Fleur, S. E.; Nicolaou, M. , How exposure to chronic stress contributes to the development of type 2 diabetes: A complexity science approach. Front. Neuroendocrinol. 2022, 65, 100972. [Google Scholar] [CrossRef] [PubMed]
- Fahed, G.; Aoun, L.; Bou Zerdan, M.; Allam, S.; Bou Zerdan, M.; Bouferraa, Y.; Assi, H.I. Metabolic Syndrome: Updates on Pathophysiology and Management in 2021. Int. J. Mol. Sci. 2022, 23, 786. [Google Scholar] [CrossRef]
- Giacco, F.; Brownlee, M.; Schmidt, A. M. , Oxidative Stress and Diabetic Complications. Circ. Res. 2010, 107, 1058–1070. [Google Scholar] [CrossRef]
- Akpoveso, O.-O.P.; Ubah, E.E.; Obasanmi, G. Antioxidant Phytochemicals as Potential Therapy for Diabetic Complications. Antioxidants 2023, 12, 123. [Google Scholar] [CrossRef]
- Newman, D. J.; Cragg, G. M. , Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019. J. Nat. Prod. 2020, 83, 770–803. [Google Scholar] [CrossRef]
- Dias, D.A.; Urban, S.; Roessner, U. A Historical Overview of Natural Products in Drug Discovery. Metabolites 2012, 2, 303–336. [Google Scholar] [CrossRef]
- Abbas, G.; Al Harrasi, A.; Hussain, H.; Hamaed, A.; Supuran, C. T. , The management of diabetes mellitus-imperative role of natural products against dipeptidyl peptidase-4, α-glucosidase and sodium-dependent glucose co-transporter 2 (SGLT2). Bioorg.Chem. 2019, 86, 305–315. [Google Scholar] [CrossRef]
- Vivó-Barrachina, L.; Rojas-Chacón, M.J.; Navarro-Salazar, R.; Belda-Sanchis, V.; Pérez-Murillo, J.; Peiró-Puig, A.; Herran-González, M.; Pérez-Bermejo, M. The Role of Natural Products on Diabetes Mellitus Treatment: A Systematic Review of Randomized Controlled Trials. Pharmaceutics 2022, 14, 101. [Google Scholar] [CrossRef]
- Magwaza, S.N.; Islam, M.S. Roles of Marine Macroalgae or Seaweeds and Their Bioactive Compounds in Combating Overweight, Obesity and Diabetes: A Comprehensive Review. Mar. Drugs 2023, 21, 258. [Google Scholar] [CrossRef]
- Menaa, F.; Wijesinghe, U.; Thiripuranathar, G.; Althobaiti, N.A.; Albalawi, A.E.; Khan, B.A.; Menaa, B. Marine Algae-Derived Bioactive Compounds: A New Wave of Nanodrugs? Mar. Drugs 2021, 19, 484. [Google Scholar] [CrossRef] [PubMed]
- Bocanegra, A.; Macho-González, A.; Garcimartín, A.; Benedí, J.; Sánchez-Muniz, F.J. Whole Alga, Algal Extracts, and Compounds as Ingredients of Functional Foods: Composition and Action Mechanism Relationships in the Prevention and Treatment of Type-2 Diabetes Mellitus. Int. J. Mol. Sci. 2021, 22, 3816. [Google Scholar] [CrossRef]
- Pradhan, B.; Nayak, R.; Patra, S.; Jit, B.P.; Ragusa, A.; Jena, M. Bioactive Metabolites from Marine Algae as Potent Pharmacophores against Oxidative Stress-Associated Human Diseases: A Comprehensive Review. Molecules 2021, 26, 37. [Google Scholar] [CrossRef] [PubMed]
- Zhou, J.; Chen, B. Retinal Cell Damage in Diabetic Retinopathy. Cells 2023, 12, 1342. [Google Scholar] [CrossRef]
- Jin, Y.; Arroo, R. , The protective effects of flavonoids and carotenoids against diabetic complications—A review of in vivo evidence. Front. Nutr. 2023, 10. [Google Scholar] [CrossRef]
- Pham, T.K.; Nguyen, T.H.T.; Yun, H.R.; Vasileva, E.A.; Mishchenko, N.P.; Fedoreyev, S.A.; Stonik, V.A.; Vu, T.T.; Nguyen, H.Q.; Cho, S.W.; et al. Echinochrome A Prevents Diabetic Nephropathy by Inhibiting the PKC-Iota Pathway and Enhancing Renal Mitochondrial Function in db/db Mice. Mar. Drugs 2023, 21, 222. [Google Scholar] [CrossRef]
- Wang, Y.; Sui, Z.; Wang, M.; Liu, P. , Natural products in attenuating renal inflammation via inhibiting the NLRP3 inflammasome in diabetic kidney disease Front. Immunol. 2023, 14. [Google Scholar] [CrossRef]
- Hempel, M.d.S.S.; Colepicolo, P.; Zambotti-Villela, L. Macroalgae Biorefinery for the Cosmetic Industry: Basic Concept, Green Technology, and Safety Guidelines. Phycology 2023, 3, 211–241. [Google Scholar] [CrossRef]
- Arora, K.; Kumar, P.; Bose, D.; Li, X.; Kulshrestha, S. Potential applications of algae in biochemical and bioenergy sector. 3 Biotech 2021, 11, 296. [Google Scholar] [CrossRef]
- Alam, S.; Sarker, M. M. R.; Sultana, T. N.; Chowdhury, M. N. R.; Rashid, M. A.; Chaity, N. I.; Zhao, C.; Xiao, J.; Hafez, E. E.; Khan, S. A.; Mohamed, I. N. , Antidiabetic Phytochemicals From Medicinal Plants: Prospective Candidates for New Drug Discovery and Development. Front. Endocrinol. 2022, 13. [Google Scholar] [CrossRef]
- Lankatillake, C.; Huynh, T.; Dias, D. A. , Understanding glycaemic control and current approaches for screening antidiabetic natural products from evidence-based medicinal plants. Plant Methods 2019, 15, 105. [Google Scholar] [CrossRef] [PubMed]
- Subermaniam, K.; Teoh, S. L.; Yow, Y. Y.; Tang, Y. Q.; Lim, L. W.; Wong, K. H. Marine algae as emerging therapeutic alternatives for depression: A review. Iran J. Basic Med. Sci. 2021, 24, 997–1013. [Google Scholar] [CrossRef]
- Popović-Djordjević, B. J.; Katanić Stanković, S. J.; Mihailović, V.; Pereira, G. A.; Garcia-Oliveira, P.; Prieto, A. M.; Simal-Gandara, J. , Algae as a Source of Bioactive Compounds to Prevent the Development of Type 2 Diabetes Mellitus. Curr. Med. Chem. 2021, 28, 4592–4615. [Google Scholar] [CrossRef]
- Khaligh, S. F.; Asoodeh, A. , Recent advances in the bio-application of microalgae-derived biochemical metabolites and development trends of photobioreactor-based culture systems. 3 Biotech 2022, 12, 260. [Google Scholar] [CrossRef] [PubMed]
- Zhuang, D.; He, N.; Khoo, K. S.; Ng, E.-P.; Chew, K. W.; Ling, T. C. , Application progress of bioactive compounds in microalgae on pharmaceutical and cosmetics. Chemosphere 2022, 291, 132932. [Google Scholar] [CrossRef] [PubMed]
- Ramanan, R.; Kim, B.-H.; Cho, D.-H.; Oh, H.-M.; Kim, H.-S. , Algae–bacteria interactions: Evolution, ecology and emerging applications. Biotechnology Advances 2016, 34, 14–29. [Google Scholar] [CrossRef]
- Pereira, L. Macroalgae. Encyclopedia 2021, 1, 177–188. [Google Scholar] [CrossRef]
- Dolganyuk, V.; Belova, D.; Babich, O.; Prosekov, A.; Ivanova, S.; Katserov, D.; Patyukov, N.; Sukhikh, S. Microalgae: A Promising Source of Valuable Bioproducts. Biomolecules 2020, 10, 1153. [Google Scholar] [CrossRef]
- Silva, M.; Kamberovic, F.; Uota, S.T.; Kovan, I.-M.; Viegas, C.S.B.; Simes, D.C.; Gangadhar, K.N.; Varela, J.; Barreira, L. Microalgae as Potential Sources of Bioactive Compounds for Functional Foods and Pharmaceuticals. Appl. Sci. 2022, 12, 5877. [Google Scholar] [CrossRef]
- Menaa, F.; Wijesinghe, P.A.U.I.; Thiripuranathar, G.; Uzair, B.; Iqbal, H.; Khan, B.A.; Menaa, B. Ecological and Industrial Implications of Dynamic Seaweed-Associated Microbiota Interactions. Mar. Drugs 2020, 18, 641. [Google Scholar] [CrossRef]
- Pereira, L.; Gheda, S. F.; Ribeiro-Claro, P. J. A. , Analysis by Vibrational Spectroscopy of Seaweed Polysaccharides with Potential Use in Food, Pharmaceutical, and Cosmetic Industries. Int. J. Carbohydr. Chem. 2013, 2013, 537202. [Google Scholar] [CrossRef]
- Li, Y.; Zheng, Y.; Zhang, Y.; Yang, Y.; Wang, P.; Imre, B.; Wong, A.C.Y.; Hsieh, Y.S.Y.; Wang, D. Brown Algae Carbohydrates: Structures, Pharmaceutical Properties, and Research Challenges. Mar. Drugs 2021, 19, 620. [Google Scholar] [CrossRef]
- Araújo, R.; Vázquez Calderón, F.; Sánchez López, J.; Azevedo, I. C.; Bruhn, A.; Fluch, S.; Garcia Tasende, M.; Ghaderiardakani, F.; Ilmjärv, T.; Laurans, M.; Mac Monagail, M.; Mangini, S.; Peteiro, C.; Rebours, C.; Stefansson, T.; Ullmann, J. , Current Status of the Algae Production Industry in Europe: An Emerging Sector of the Blue Bioeconomy. Front. Mar. Sci. 2021, 7. [Google Scholar] [CrossRef]
- Fabris, M.; Abbriano, R. M.; Pernice, M.; Sutherland, D. L.; Commault, A. S.; Hall, C. C.; Labeeuw, L.; McCauley, J. I.; Kuzhiuparambil, U.; Ray, P.; Kahlke, T.; Ralph, P. J. , Emerging Technologies in Algal Biotechnology: Toward the Establishment of a Sustainable, Algae-Based Bioeconomy. Front. Plant Sci. 2020, 11. [Google Scholar] [CrossRef]
- Lourenço-Lopes, C.; Fraga-Corral, M.; Jimenez-Lopez, C.; Pereira, A.G.; Garcia-Oliveira, P.; Carpena, M.; Prieto, M.A.; Simal-Gandara, J. Metabolites from Macroalgae and Its Applications in the Cosmetic Industry: A Circular Economy Approach. Resources 2020, 9, 101. [Google Scholar] [CrossRef]
- Wainwright, C. L.; Teixeira, M. M.; Adelson, D. L.; Braga, F. C.; Buenz, E. J.; Campana, P. R. V.; David, B.; Glaser, K. B.; Harata-Lee, Y.; Howes, M.-J. R.; Izzo, A. A.; Maffia, P.; Mayer, A. M. S.; Mazars, C.; Newman, D. J.; Nic Lughadha, E.; Pádua, R. M.; Pimenta, A. M. C.; Parra, J. A. A.; Qu, Z.; Shen, H.; Spedding, M.; Wolfender, J.-L. , Future directions for the discovery of natural product-derived immunomodulating drugs: an IUPHAR positional review. Pharmacol. Res. 2022, 177, 106076. [Google Scholar] [CrossRef]
- Lu, L.W.; Chen, J.-H. Seaweeds as Ingredients to Lower Glycemic Potency of Cereal Foods Synergistically—A Perspective. Foods 2022, 11, 714. [Google Scholar] [CrossRef]
- Bhuyan, P.P.; Nayak, R.; Patra, S.; Abdulabbas, H.S.; Jena, M.; Pradhan, B. Seaweed-Derived Sulfated Polysaccharides; The New Age Chemopreventives: A Comprehensive Review. Cancers 2023, 15, 715. [Google Scholar] [CrossRef]
- Rathod, N.B.; Elabed, N.; Punia, S.; Ozogul, F.; Kim, S.-K.; Rocha, J.M. Recent Developments in Polyphenol Applications on Human Health: A Review with Current Knowledge. Plants 2023, 12, 1217. [Google Scholar] [CrossRef]
- Rudrapal, M.; Khairnar, S. J.; Khan, J.; Dukhyil, A. B.; Ansari, M. A.; Alomary, M. N.; Alshabrmi, F. M.; Palai, S.; Deb, P. K.; Devi, R. , Dietary Polyphenols and Their Role in Oxidative Stress-Induced Human Diseases: Insights Into Protective Effects, Antioxidant Potentials and Mechanism(s) of Action. Front. Pharmacol. 2022, 13. [Google Scholar] [CrossRef]
- Figueiredo, F.; Encarnação, T.; Campos, M. Algae as Functional Foods for the Elderly. Food and Nutrition Sciences 2016, 7, 1122–1148. [Google Scholar] [CrossRef]
- Sinha, S.; Haque, M.; Lugova, H.; Kumar, S. The Effect of Omega-3 Fatty Acids on Insulin Resistance. Life 2023, 13, 1322. [Google Scholar] [CrossRef]
- Conde, T.A.; Zabetakis, I.; Tsoupras, A.; Medina, I.; Costa, M.; Silva, J.; Neves, B.; Domingues, P.; Domingues, M.R. Microalgal Lipid Extracts Have Potential to Modulate the Inflammatory Response: A Critical Review. Int. J. Mol. Sci. 2021, 22, 9825. [Google Scholar] [CrossRef] [PubMed]
- Echave, J.; Otero, P.; Garcia-Oliveira, P.; Munekata, P.E.S.; Pateiro, M.; Lorenzo, J.M.; Simal-Gandara, J.; Prieto, M.A. Seaweed-Derived Proteins and Peptides: Promising Marine Bioactives. Antioxidants 2022, 11, 176. [Google Scholar] [CrossRef]
- Zhao, C.; Yang, C.; Liu, B.; Lin, L.; Sarker, S. D.; Nahar, L.; Yu, H.; Cao, H.; Xiao, J. , Bioactive compounds from marine macroalgae and their hypoglycemic benefits. Trends Food Sci. Technol. 2018, 72, 1–12. [Google Scholar] [CrossRef]
- Sharifuddin, Y.; Chin, Y.-X.; Lim, P.-E.; Phang, S.-M. Potential Bioactive Compounds from Seaweed for Diabetes Management. Mar. Drugs 2015, 13, 5447–5491. [Google Scholar] [CrossRef] [PubMed]
- Attjioui, M.; Ryan, S.; Ristic, A. K.; Higgins, T.; Goñi, O.; Gibney, E. R.; Tierney, J.; O'Connell, S. Comparison of edible brown algae extracts for the inhibition of intestinal carbohydrate digestive enzymes involved in glucose release from the diet. J. Nutr. Sci. 2021, 10, e5. [Google Scholar] [CrossRef]
- Melloni, M.; Sergi, D.; Simioni, C.; Passaro, A.; Neri, L.M. Microalgae as a Nutraceutical Tool to Antagonize the Impairment of Redox Status Induced by SNPs: Implications on Insulin Resistance. Biology 2023, 12, 449. [Google Scholar] [CrossRef]
- Naz, R.; Saqib, F.; Awadallah, S.; Wahid, M.; Latif, M.F.; Iqbal, I.; Mubarak, M.S. Food Polyphenols and Type II Diabetes Mellitus: Pharmacology and Mechanisms. Molecules 2023, 28, 3996. [Google Scholar] [CrossRef]
- Tan, B. L.; Norhaizan, M. E.; Liew, W.-P.-P.; Sulaiman Rahman, H. Antioxidant and Oxidative Stress: A Mutual Interplay in Age-Related Diseases. Front. Pharmacol. 2018, 9. [Google Scholar] [CrossRef] [PubMed]
- Pheiffer, C.; Dias, S.; Jack, B.; Malaza, N.; Adam, S. Adiponectin as a Potential Biomarker for Pregnancy Disorders. Int. J. Mol. Sci. 2021, 22, 1326. [Google Scholar] [CrossRef] [PubMed]
- Tamel Selvan, K.; Goon, J.A.; Makpol, S.; Tan, J.K. Effects of Microalgae on Metabolic Syndrome. Antioxidants 2023, 12, 449. [Google Scholar] [CrossRef] [PubMed]
- Kang, Q.; Yang, C. Oxidative stress and diabetic retinopathy: Molecular mechanisms, pathogenetic role and therapeutic implications. Redox Biology 2020, 37, 101799. [Google Scholar] [CrossRef] [PubMed]
- Khan, M. A.; Kassianos, A. J.; Hoy, W. E.; Alam, A. K.; Healy, H. G.; Gobe, G. C. , Promoting Plant-Based Therapies for Chronic Kidney Disease. J. Evid. Based. Integr. Med. 2022, 27, 2515690X221079688. [Google Scholar] [CrossRef]
- Nyakundi, B.B.; Yang, J. Uses of Papaya Leaf and Seaweed Supplementations for Controlling Glucose Homeostasis in Diabetes. Int. J. Mol. Sci. 2023, 24, 6846. [Google Scholar] [CrossRef]
- Shehadeh, M.B.; Suaifan, G.A.R.Y.; Abu-Odeh, A.M. Plants Secondary Metabolites as Blood Glucose-Lowering Molecules. Molecules 2021, 26, 4333. [Google Scholar] [CrossRef]
- Sahakyan, G.; Vejux, A.; Sahakyan, N. The Role of Oxidative Stress-Mediated Inflammation in the Development of T2DM-Induced Diabetic Nephropathy: Possible Preventive Action of Tannins and Other Oligomeric Polyphenols. Molecules 2022, 27, 9035. [Google Scholar] [CrossRef]
- Rahman, M. M.; Dhar, P. S.; Sumaia; Anika, F. ; Ahmed, L.; Islam, M. R.; Sultana, N. A.; Cavalu, S.; Pop, O.; Rauf, A., Exploring the plant-derived bioactive substances as antidiabetic agent: An extensive review. Biomed. Pharmacother. 2022, 152, 113217. [Google Scholar] [CrossRef]
- Janssen, J.A.M.J.L. Hyperinsulinemia and Its Pivotal Role in Aging, Obesity, Type 2 Diabetes, Cardiovascular Disease and Cancer. Int. J. Mol. Sci. 2021, 22, 7797. [Google Scholar] [CrossRef]
- de Sousa Neto, I.V.; Durigan, J.L.Q.; da Silva, A.S.R.; de Cássia Marqueti, R. Adipose Tissue Extracellular Matrix Remodeling in Response to Dietary Patterns and Exercise: Molecular Landscape, Mechanistic Insights, and Therapeutic Approaches. Biology 2022, 11, 765. [Google Scholar] [CrossRef] [PubMed]
- Sangwung, P.; Petersen, K. F.; Shulman, G. I.; Knowles, J. W. Mitochondrial Dysfunction, Insulin Resistance, and Potential Genetic Implications: Potential Role of Alterations in Mitochondrial Function in the Pathogenesis of Insulin Resistance and Type 2 Diabetes. Endocrinology 2020, 161. [Google Scholar] [CrossRef]
- Vignaud, J.; Loiseau, C.; Hérault, J.; Mayer, C.; Côme, M.; Martin, I.; Ulmann, L. Microalgae Produce Antioxidant Molecules with Potential Preventive Effects on Mitochondrial Functions and Skeletal Muscular Oxidative Stress. Antioxidants 2023, 12, 1050. [Google Scholar] [CrossRef]
- Ouahabi, S.; Loukili, E.H.; Daoudi, N.E.; Chebaibi, M.; Ramdani, M.; Rahhou, I.; Bnouham, M.; Fauconnier, M.-L.; Hammouti, B.; Rhazi, L.; et al. Study of the Phytochemical Composition, Antioxidant Properties, and In Vitro Anti-Diabetic Efficacy of Gracilaria bursa-pastoris Extracts. Mar. Drugs 2023, 21, 372. [Google Scholar] [CrossRef]
- Kashtoh, H.; Baek, K.-H. Recent Updates on Phytoconstituent Alpha-Glucosidase Inhibitors: An Approach towards the Treatment of Type Two Diabetes. Plants 2022, 11, 2722. [Google Scholar] [CrossRef]
- Kicel, A.; Magiera, A.; Skrzywanek, M.; Malczuk, M.; Olszewska, M. A. The Inhibition of α-Glucosidase, α-Amylase and Protein Glycation by Phenolic Extracts of Cotoneaster bullatus, Cotoneaster zabelii, and Cotoneaster integerrimus Leaves and Fruits: Focus on Anti-Hyperglycemic Activity and Kinetic Parameters. Molecules 2022, 27, 7081. [Google Scholar] [CrossRef] [PubMed]
- Unnikrishnan, P. S.; Suthindhiran, K.; Jayasri, M. A. Alpha-amylase Inhibition and Antioxidant Activity of Marine Green Algae and its Possible Role in Diabetes Management. Pharmacogn Mag. 2015, 11, S511–S515. [Google Scholar] [CrossRef] [PubMed]
- Yin, S.; Siahaan, E. A.; Niu, L.; Shibata, M.; Liu, Y.; Hagiwara, T. Real time monitoring and evaluation of the inhibition effect of fucoxanthin against α-amylase activity by using QCM-A. Front. Nutr. 2023, 9. [Google Scholar] [CrossRef]
- Ćorković, I.; Gašo-Sokač, D.; Pichler, A.; Šimunović, J.; Kopjar, M. Dietary Polyphenols as Natural Inhibitors of α-Amylase and α-Glucosidase. Life 2022, 12, 1692. [Google Scholar] [CrossRef]
- Gazali, M.; Jolanda, O.; Husni, A.; Nurjanah; Majid, F.A.A.; Zuriat; Syafitri, R. In Vitro α-Amylase and α-Glucosidase Inhibitory Activity of Green Seaweed Halimeda tuna Extract from the Coast of Lhok Bubon, Aceh. Plants 2023, 12, 393. [CrossRef]
- Truong, T. P. T.; Tran, T. M.; Dai, T. X. T.; Tran, C. L. Antihyperglycemic and anti-type 2 diabetic activity of marine hydroquinone isolated from brown algae (Dictyopteris polypodioides). J. Tradit. Complement. Med. 2023, 13, 408–416. [Google Scholar] [CrossRef]
- Lauritano, C.; Ianora, A. Marine Organisms with Anti-Diabetes Properties. Mar. Drugs 2016, 14, 220. [Google Scholar] [CrossRef] [PubMed]
- Rezzola, S.; Loda, A.; Corsini, M.; Semeraro, F.; Annese, T.; Presta, M.; Ribatti, D. , Angiogenesis-Inflammation Cross Talk in Diabetic Retinopathy: Novel Insights from the Chick Embryo Chorioallantoic Membrane/Human Vitreous Platform. Front. Immunol. 2020, 11. [Google Scholar] [CrossRef] [PubMed]
- Méresse, S.; Fodil, M.; Fleury, F.; Chénais, B. Fucoxanthin, a Marine-Derived Carotenoid from Brown Seaweeds and Microalgae: A Promising Bioactive Compound for Cancer Therapy. Int. J. Mol. Sci. 2020, 21, 9273. [Google Scholar] [CrossRef] [PubMed]
- Kowluru, R. A.; Chan, P.-S. , Oxidative Stress and Diabetic Retinopathy. Experimental Diabetes Research 2007, 2007, 043603. [Google Scholar] [CrossRef]
- Brillante, S.; Galasso, C.; Lauritano, C.; Carrella, S. , From the Sea for the Sight: Marine Derived Products for Human Vision. Front. Aging Neurosci. 2022, 14. [Google Scholar] [CrossRef]
- Fathalipour M, Fathalipour H, Safa O, Nowrouzi-Sohrabi P, Mirkhani H, Hassanipour S. The Therapeutic Role of Carotenoids in Diabetic Retinopathy: A Systematic Review. Diabetes Metab Syndr Obes. 2020, 13, 2347–2358. [Google Scholar] [CrossRef]
- El-Baz, F. K.; Salama, A.; Salama, R. A. A. , Dunaliella salina Attenuates Diabetic Neuropathy Induced by STZ in Rats: Involvement of Thioredoxin. BioMed Research International 2020, 2020, 1295492. [Google Scholar] [CrossRef]
- Rudraraju, M.; Narayanan, S. P.; Somanath, P. R. , Regulation of blood-retinal barrier cell-junctions in diabetic retinopathy. Pharmacol Res. 2020, 161, 105115. [Google Scholar] [CrossRef]
- Chiang, Y.-F.; Chen, H.-Y.; Chang, Y.-J.; Shih, Y.-H.; Shieh, T.-M.; Wang, K.-L.; Hsia, S.-M. Protective Effects of Fucoxanthin on High Glucose- and 4-Hydroxynonenal (4-HNE)-Induced Injury in Human Retinal Pigment Epithelial Cells. Antioxidants 2020, 9, 1176. [Google Scholar] [CrossRef]
- Robles-Rivera, R. R.; Castellanos-González, J. A.; Olvera-Montaño, C.; Flores-Martin, R. A.; López-Contreras, A. K.; Arevalo-Simental, D. E.; Cardona-Muñoz, E. G.; Roman-Pintos, L. M.; Rodríguez-Carrizalez, A. D. , Adjuvant Therapies in Diabetic Retinopathy as an Early Approach to Delay Its Progression: The Importance of Oxidative Stress and Inflammation. Oxidative Medicine and Cellular Longevity 2020, 2020, 3096470. [Google Scholar] [CrossRef] [PubMed]
- Rayapu, L.; Chakraborty, K.; Valluru, L. (2021). Marine Algae as a Potential Source for Anti-diabetic Compounds - A Brief Review. Curr. Pharm. Des. 2021, 27, 789–801. [Google Scholar] [CrossRef]
- Catarino, M.D.; Marçal, C.; Bonifácio-Lopes, T.; Campos, D.; Mateus, N.; Silva, A.M.S.; Pintado, M.M.; Cardoso, S.M. Impact of Phlorotannin Extracts from Fucus vesiculosus on Human Gut Microbiota. Mar. Drugs 2021, 19, 375. [Google Scholar] [CrossRef] [PubMed]
- Guo, D.; Yu, K.; Sun, X.-Y.; Ouyang, J.-M. , Structural Characterization and Repair Mechanism of Gracilaria lemaneiformis Sulfated Polysaccharides of Different Molecular Weights on Damaged Renal Epithelial Cells. Oxidative Medicine and Cellular Longevity 2018, 2018, 7410389. [Google Scholar] [CrossRef]
- Sanayei, M.; Kalejahi, P.; Mahinkazemi, M.; Fathifar, Z.; Barzegar, A. , The effect of Chlorella vulgaris on obesity related metabolic disorders: a systematic review of randomized controlled trials. Journal of Complementary and Integrative Medicine 2022, 19, 833–842. [Google Scholar] [CrossRef]
- Fallah, A. A.; Sarmast, E.; Habibian Dehkordi, S.; Engardeh, J.; Mahmoodnia, L.; Khaledifar, A.; Jafari, T. Effect of Chlorella supplementation on cardiovascular risk factors: A meta-analysis of randomized controlled trials. Clinical Nutrition 2018, 37, 1892–1901. [Google Scholar] [CrossRef] [PubMed]
- Hannan, J. M. A.; Ansari, P.; Azam, S.; Flatt, P. R.; Abdel Wahab, Y. H. A. Effects of Spirulina platensis on insulin secretion, dipeptidyl peptidase IV activity and both carbohydrate digestion and absorption indicate potential as an adjunctive therapy for diabetes. Br J Nutr. 2020, 124, 1021–1034. [Google Scholar] [CrossRef]
- Hatami, E.; Ghalishourani, S.-S.; Najafgholizadeh, A.; Pourmasoumi, M.; Hadi, A.; Clark, C. C. T.; Assaroudi, M.; Salehi-sahlabadi, A.; Joukar, F.; Mansour-Ghanaei, F. , The effect of spirulina on type 2 diabetes: a systematic review and meta-analysis. J. Diabetes Metab. Disord. 2021, 20, 883–892. [Google Scholar] [CrossRef]
- Koirala, P.; Jung, H. A.; Choi, J. S. , Recent advances in pharmacological research on Ecklonia species: a review. Arch. Pharm. Res. 2017, 40, 981–1005. [Google Scholar] [CrossRef]
- Mawed, S.A.; Centoducati, G.; Farag, M.R.; Alagawany, M.; Abou-Zeid, S.M.; Elhady, W.M.; El-Saadony, M.T.; Di Cerbo, A.; Al-Zahaby, S.A. Dunaliella salina Microalga Restores the Metabolic Equilibrium and Ameliorates the Hepatic Inflammatory Response Induced by Zinc Oxide Nanoparticles (ZnO-NPs) in Male Zebrafish. Biology 2022, 11, 1447. [Google Scholar] [CrossRef]
- Cho, C.-H.; Yoo, G.; Kim, M.; Kurniawati, U.D.; Choi, I.-W.; Lee, S.-H. Dieckol, Derived from the Edible Brown Algae Ecklonia cava, Attenuates Methylglyoxal-Associated Diabetic Nephropathy by Suppressing AGE–RAGE Interaction. Antioxidants 2023, 12, 593. [Google Scholar] [CrossRef]
- Kumari, A.; Garima; Bharadvaja, N. , A comprehensive review on algal nutraceuticals as prospective therapeutic agent for different diseases. 3 Biotech 2023, 13, 44. [Google Scholar] [CrossRef] [PubMed]
- Jo, S.-L.; Yang, H.; Jeong, K.-J.; Lee, H.-W.; Hong, E.-J. Neuroprotective Effects of Ecklonia cava in a Chronic Neuroinflammatory Disease Model. Nutrients 2023, 15, 2007. [Google Scholar] [CrossRef] [PubMed]
- Shibasaki, S.; Ueda, M. Utilization of Macroalgae for the Production of Bioactive Compounds and Bioprocesses Using Microbial Biotechnology. Microorganisms 2023, 11, 1499. [Google Scholar] [CrossRef] [PubMed]
- Mahendran, S.; Maheswari, P.; Sasikala, V.; Rubika, J. j.; Pandiarajan, J. In vitro antioxidant study of polyphenol from red seaweeds dichotomously branched gracilaria Gracilaria edulis and robust sea moss Hypnea valentiae. Toxicol. Rep. 2021, 8, 1404–1411. [Google Scholar] [CrossRef]
- Martins, B.; Vieira, M.; Delerue-Matos, C.; Grosso, C.; Soares, C. Biological Potential, Gastrointestinal Digestion, Absorption, and Bioavailability of Algae-Derived Compounds with Neuroprotective Activity: A Comprehensive Review. Mar. Drugs 2022, 20, 362. [Google Scholar] [CrossRef]
- Choi, J.; Kim, K.-J.; Koh, E.-J.; Lee, B.-Y. Gelidium elegans Extract Ameliorates Type 2 Diabetes via Regulation of MAPK and PI3K/Akt Signaling. Nutrients 2018, 10, 51. [Google Scholar] [CrossRef]
- Pereira, L.; Valado, A. The Seaweed Diet in Prevention and Treatment of the Neurodegenerative Diseases. Mar. Drugs 2021, 19, 128. [Google Scholar] [CrossRef]
- Babich, O.; Sukhikh, S.; Larina, V.; Kalashnikova, O.; Kashirskikh, E.; Prosekov, A.; Noskova, S.; Ivanova, S.; Fendri, I.; Smaoui, S.; et al. Algae: Study of Edible and Biologically Active Fractions, Their Properties and Applications. Plants 2022, 11, 780. [Google Scholar] [CrossRef]
- Gabbia, D.; De Martin, S. Brown Seaweeds for the Management of Metabolic Syndrome and Associated Diseases. Molecules 2020, 25, 4182. [Google Scholar] [CrossRef]
- Hao, S.; Li, F.; Li, Q.; Yang, Q.; Zhang, W. Phycocyanin Protects against High Glucose High Fat Diet Induced Diabetes in Mice and Participates in AKT and AMPK Signaling. Foods 2022, 11, 3183. [Google Scholar] [CrossRef]
- Din, N.A.S.; Mohd Alayudin, ‘A. S.; Sofian-Seng, N.-S.; Rahman, H.A.; Mohd Razali, N.S.; Lim, S.J.; Wan Mustapha, W.A. Brown Algae as Functional Food Source of Fucoxanthin: A Review. Foods 2022, 11, 2235. [Google Scholar] [CrossRef]
- Sugii, S.; Olson, P.; Sears, D. D.; Saberi, M.; Atkins, A. R.; Barish, G. D.; Hong, S.-H.; Castro, G. L.; Yin, Y.-Q.; Nelson, M. C.; Hsiao, G.; Greaves, D. R. Downes, M.; Yu, R. T.; Olefsky, J. M.; Evans, R. M., PPARγ activation in adipocytes is sufficient for systemic insulin sensitization. PNAS 2009, 106, 22504–22509. [Google Scholar] [CrossRef]
- Kim, K.-T.; Rioux, L.-E.; Turgeon, S. L. Alpha-amylase and alpha-glucosidase inhibition is differentially modulated by fucoidan obtained from Fucus vesiculosus and Ascophyllum nodosum. Phytochem. 2014, 98, 27–33. [Google Scholar] [CrossRef]
- Zheng, H.; Zhao, Y.; Guo, L. A Bioactive Substance Derived from Brown Seaweeds: Phlorotannins. Mar. Drugs 2022, 20, 742. [Google Scholar] [CrossRef] [PubMed]
- Kim, J.; Choi, J.H.; Ko, G.; Jo, H.; Oh, T.; Ahn, B.; Unno, T. Anti-Inflammatory Properties and Gut Microbiota Modulation of Porphyra tenera Extracts in Dextran Sodium Sulfate-Induced Colitis in Mice. Antioxidants 2020, 9, 988. [Google Scholar] [CrossRef] [PubMed]
- Gentscheva, G.; Nikolova, K.; Panayotova, V.; Peycheva, K.; Makedonski, L.; Slavov, P.; Radusheva, P.; Petrova, P.; Yotkovska, I. Application of Arthrospira platensis for Medicinal Purposes and the Food Industry: A Review of the Literature. Life 2023, 13, 845. [Google Scholar] [CrossRef]
- Unnikrishnan, P.S.; Animish, A.; Madhumitha, G.; Suthindhiran, K.; Jayasri, M.A. Bioactivity Guided Study for the Isolation and Identification of Antidiabetic Compounds from Edible Seaweed—Ulva reticulata. Molecules 2022, 27, 8827. [Google Scholar] [CrossRef] [PubMed]
- Mumu, M.; Das, A.; Emran, T. B.; Mitra, S.; Islam, F.; Roy, A.; Karim, M. M.; Das, R.; Park, M. N.; Chandran, D.; Sharma, R.; Khandaker, M. U.; Idris, A. M.; Kim, B. Fucoxanthin: A Promising Phytochemical on Diverse Pharmacological Targets. Front. Pharmacol. 2022, 13. [Google Scholar] [CrossRef] [PubMed]
- Wu, D.; Chen, Y.; Wan, X.; Liu, D.; Wen, Y.; Chen, X.; Zhao, C. , Structural characterization and hypoglycemic effect of green alga Ulva lactuca oligosaccharide by regulating microRNAs in Caenorhabditis elegans. Algal Res. 2020, 51, 102083. [Google Scholar] [CrossRef]
- Wang, X.; Shan, X.; Dun, Y.; Cai, C.; Hao, J.; Li, G.; Cui, K.; Yu, G. Anti-Metabolic Syndrome Effects of Fucoidan from Fucus vesiculosus via Reactive Oxygen Species-Mediated Regulation of JNK, Akt, and AMPK Signaling. Molecules 2019, 24, 3319. [Google Scholar] [CrossRef] [PubMed]
- Lopes, G.; Andrade, P.B.; Valentão, P. Phlorotannins: Towards New Pharmacological Interventions for Diabetes Mellitus Type 2. Molecules 2017, 22, 56. [Google Scholar] [CrossRef] [PubMed]
- Tsuge, K.; Okabe, M.; Yoshimura, T.; Sumi, T.; Tachibana, H.; Yamada, K. Dietary Effects of Porphyran from Porphyra yezoensis on Growth and Lipid Metabolism of Sprague-Dawley Rats. Food Sci. Technol. Res. 2004, 10, 147–151. [Google Scholar] [CrossRef]
- Besednova, N.N.; Andryukov, B.G.; Zaporozhets, T.S.; Kuznetsova, T.A.; Kryzhanovsky, S.P.; Ermakova, S.P.; Galkina, I.V.; Shchelkanov, M.Y. Molecular Targets of Brown Algae Phlorotannins for the Therapy of Inflammatory Processes of Various Origins. Mar. Drugs 2022, 20, 243. [Google Scholar] [CrossRef]
- Jayasinghe, A.M.K.; Kirindage, K.G.I.S.; Fernando, I.P.S.; Kim, K.-N.; Oh, J.-Y.; Ahn, G. The Anti-Inflammatory Effect of Low Molecular Weight Fucoidan from Sargassum siliquastrum in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages via Inhibiting NF-κB/MAPK Signaling Pathways. Mar. Drugs 2023, 21, 347. [Google Scholar] [CrossRef]
- Imbimbo, P.; D’Elia, L.; Liberti, D.; Olivieri, G.; Monti, D. M. Towards green extraction methods from microalgae learning from the classics. Appl. Microbiol. Biotechnol. 2020, 104, 9067–9077. [Google Scholar] [CrossRef]
- Pateiro, M.; Gómez, B.; Munekata, P.E.S.; Barba, F.J.; Putnik, P.; Kovačević, D.B.; Lorenzo, J.M. Nanoencapsulation of Promising Bioactive Compounds to Improve Their Absorption, Stability, Functionality and the Appearance of the Final Food Products. Molecules 2021, 26, 1547. [Google Scholar] [CrossRef] [PubMed]
- Dewanjee, S.; Chakraborty, P.; Mukherjee, B.; De Feo, V. Plant-Based Antidiabetic Nanoformulations: The Emerging Paradigm for Effective Therapy. Int. J. Mol. Sci. 2020, 21, 2217. [Google Scholar] [CrossRef]
- Wells, M. L.; Potin, P.; Craigie, J. S.; Raven, J. A.; Merchant, S. S.; Helliwell, K. E.; Smith, A. G.; Camire, M. E.; Brawley, S. H. Algae as nutritional and functional food sources: revisiting our understanding. J. Appl. Phycol. 2017, 29, 949–982. [Google Scholar] [CrossRef]
- Lee, S.-H.; Jung, K.; Chung, J.; Lee, Y.-W. Comparative Study of Algae-Based Measurements of the Toxicity of 14 Manufactured Nanomaterials. Int. J. Environ. Res. Public Health 2022, 19, 5853. [Google Scholar] [CrossRef]
- Wang, X.; Chan, Y.S.; Wong, K.; Yoshitake, R.; Sadava, D.; Synold, T.W.; Frankel, P.; Twardowski, P.W.; Lau, C.; Chen, S. Mechanism-Driven and Clinically Focused Development of Botanical Foods as Multitarget Anticancer Medicine: Collective Perspectives and Insights from Preclinical Studies, IND Applications and Early-Phase Clinical Trials. Cancers 2023, 15, 701. [Google Scholar] [CrossRef]
- Liao, C.; Xiao, S.; Wang, X. Bench-to-bedside: Translational development landscape of biotechnology in healthcare. Health Sciences Review 2023, 7, 100097. [Google Scholar] [CrossRef]
- Lopes, G.; Andrade, P.B.; Valentão, P. Phlorotannins: Towards New Pharmacological Interventions for Diabetes Mellitus Type 2. Molecules 2017, 22, 56. [Google Scholar] [CrossRef] [PubMed]
- Ferreira de Oliveira, A. P.; Bragotto, A. P. A. Microalgae-based products: Food and public health. Future Foods 2022, 6, 100157. [Google Scholar] [CrossRef]
- Tan, J. S.; Lee, S. Y.; Chew, K. W.; Lam, M. K.; Lim, J. W.; Ho, S.-H.; Show, P. L. A review on microalgae cultivation and harvesting, and their biomass extraction processing using ionic liquids. Bioengineered 2020, 11, 116–129. [Google Scholar] [CrossRef]
- Zabot, G.L.; Schaefer Rodrigues, F.; Polano Ody, L.; Vinícius Tres, M.; Herrera, E.; Palacin, H.; Córdova-Ramos, J.S.; Best, I.; Olivera-Montenegro, L. Encapsulation of Bioactive Compounds for Food and Agricultural Applications. Polymers 2022, 14, 4194. [Google Scholar] [CrossRef]
- Klojdová, I.; Milota, T.; Smetanová, J.; Stathopoulos, C. Encapsulation: A Strategy to Deliver Therapeutics and Bioactive Compounds? Pharmaceuticals 2023, 16, 362. [Google Scholar] [CrossRef]
- N'Da, D.D. Prodrug Strategies for Enhancing the Percutaneous Absorption of Drugs. Molecules 2014, 19, 20780–20807. [Google Scholar] [CrossRef]
- Gallo, J. M. , Pharmacokinetic/ Pharmacodynamic-Driven Drug Development. Mt. Sinai J. Med. 2010, 77, 381–388. [Google Scholar] [CrossRef]
- Minich, D. M.; Bland, J. S. Personalized Lifestyle Medicine: Relevance for Nutrition and Lifestyle Recommendations. The Scientific World Journal 2013, 2013, 129841. [Google Scholar] [CrossRef]
- Kaur, M.; Bhatia, S.; Gupta, U.; Decker, E.; Tak, Y.; Bali, M.; Gupta, V. K.; Dar, R. A.; Bala, S. Microalgal bioactive metabolites as promising implements in nutraceuticals and pharmaceuticals: inspiring therapy for health benefits. Phytochem. Rev. 2023, 31. [Google Scholar] [CrossRef]
- Fernando, I. P. S.; Ryu, B.; Ahn, G.; Yeo, I.-K.; Jeon, Y.-J. Therapeutic potential of algal natural products against metabolic syndrome: A review of recent developments. Trends in Food Science & Technology 2020, 97, 286–299. [Google Scholar] [CrossRef]
- Unnikrishnan, S. P.; Jayasri, A. M. , Marine Algae as A Prospective Source for Antidiabetic Compounds – A Brief Review. Curr. Diabetes Rev. 2018, 14, 237–245. [Google Scholar] [CrossRef] [PubMed]
- Mohibbullah, M.; Haque, M.N.; Sohag, A.A.M.; Hossain, M.T.; Zahan, M.S.; Uddin, M.J.; Hannan, M.A.; Moon, I.S.; Choi, J.-S. A Systematic Review on Marine Algae-Derived Fucoxanthin: An Update of Pharmacological Insights. Mar. Drugs 2022, 20, 279. [Google Scholar] [CrossRef] [PubMed]
- Wong, J. F.; Hong, H. J.; Foo, S. C.; Yap, M. K. K.; Tan, J. W. A review on current and future advancements for commercialized microalgae species. Food Sci. Hum. Wellness 2022, 11, 1156–1170. [Google Scholar] [CrossRef]
- Ding, K.-x.; Gao, T.-l.; Xu, R.; Cai, J.; Zhang, H.-q.; Sun, Y.-y.; Zhong, F.; Ma, A.-g. Quantifying the Effect of Supplementation with Algae and Its Extracts on Glycolipid Metabolism: A Meta-Analysis of Randomized Controlled Trials. Nutrients 2020, 12, 1712. [Google Scholar] [CrossRef]
- Gheda, S.; Hamouda, R.A.; Naby, M.A.; Mohamed, T.M.; Al-Shaikh, T.M.; Khamis, A. Potent Effect of Phlorotannins Derived from Sargassum linifolium as Antioxidant and Antidiabetic in a Streptozotocin-Induced Diabetic Rats Model. Appl. Sci. 2023, 13, 4711. [Google Scholar] [CrossRef]
- Mabate, B.; Daub, C.D.; Malgas, S.; Edkins, A.L.; Pletschke, B.I. A Combination Approach in Inhibiting Type 2 Diabetes-Related Enzymes Using Ecklonia radiata Fucoidan and Acarbose. Pharmaceutics 2021, 13, 1979. [Google Scholar] [CrossRef]
- Ganesh Saratale, R.; Ponnusamy, V. K.; Jeyakumar, R. B.; Sirohi, R.; Piechota, G.; Shobana, S.; Dharmaraja, J.; Lay, C. H.; Dattatraya Saratale, G.; Seung Shin, H.; Ashokkumar, V. Microalgae cultivation strategies using cost–effective nutrient sources: Recent updates and progress towards biofuel production. Bioresour. Technol. 2022, 361, 127691. [Google Scholar] [CrossRef]
- Chauton, M. S.; Forbord, S.; Mäkinen, S.; Sarno, A.; Slizyte, R.; Mozuraityte, R.; Standal, I. B.; Skjermo, J. Sustainable resource production for manufacturing bioactives from micro- and macroalgae: Examples from harvesting and cultivation in the Nordic region. Physiol. Plant. 2021, 173, 495–506. [Google Scholar] [CrossRef]
- Marques, M.P.; Varela, C.; Mendonça, L.; Cabral, C. Nanotechnology-Based Topical Delivery of Natural Products for the Management of Atopic Dermatitis. Pharmaceutics 2023, 15, 1724. [Google Scholar] [CrossRef]
- Kyriakoudi, A.; Spanidi, E.; Mourtzinos, I.; Gardikis, K. Innovative Delivery Systems Loaded with Plant Bioactive Ingredients: Formulation Approaches and Applications. Plants 2021, 1. [Google Scholar] [CrossRef] [PubMed]
- Lomartire, S.; Gonçalves, A.M.M. Algal Phycocolloids: Bioactivities and Pharmaceutical Applications. Mar. Drugs 2023, 21, 384. [Google Scholar] [CrossRef] [PubMed]
- Kaushik, A.; Sangtani, R.; Parmar, H. S.; Bala, K. , Algal metabolites: Paving the way towards new generation antidiabetic therapeutics. Algal Res. 2023, 69, 102904. [Google Scholar] [CrossRef]
- Agarwal, S.; Singh, V.; Chauhan, K. , Antidiabetic potential of seaweed and their bioactive compounds: a review of developments in last decade. Crit. Rev. Food Sci. Nutr. 2022, 1–32. [Google Scholar] [CrossRef]
- Ahmed, M.; Semreen, A.M.; El-Huneidi, W.; Bustanji, Y.; Abu-Gharbieh, E.; Alqudah, M.A.Y.; Alhusban, A.; Shara, M.; Abuhelwa, A.Y.; Soares, N.C.; et al. Preclinical and Clinical Applications of Metabolomics and Proteomics in Glioblastoma Research. Int. J. Mol. Sci. 2023, 24, 348. [Google Scholar] [CrossRef]
- Anklam, E.; Bahl, M. I.; Ball, R.; Beger, R. D.; Cohen, J.; Fitzpatrick, S.; Girard, P.; Halamoda-Kenzaoui, B.; et al. Emerging technologies and their impact on regulatory science. Exp. Biol. Med. (Maywood) 2022, 247, 1–75. [Google Scholar] [CrossRef]
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