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Prolonged Oral Administration of Ethyl Alcohol Leads to Histopathology of the Epididymis and Seminal Vesicle and Changes of Metabolite Composition in the Tissue Lumen
Taoto, C.; Tangsrisakda, N.; Thukhammee, W.; Phetcharaburanin, J.; Iamsaard, S.; Tanphaichitr, N. Rats Orally Administered with Ethyl Alcohol for a Prolonged Time Show Histopathology of the Epididymis and Seminal Vesicle Together with Changes in the Luminal Metabolite Composition. Biomedicines2024, 12, 1010.
Taoto, C.; Tangsrisakda, N.; Thukhammee, W.; Phetcharaburanin, J.; Iamsaard, S.; Tanphaichitr, N. Rats Orally Administered with Ethyl Alcohol for a Prolonged Time Show Histopathology of the Epididymis and Seminal Vesicle Together with Changes in the Luminal Metabolite Composition. Biomedicines 2024, 12, 1010.
Taoto, C.; Tangsrisakda, N.; Thukhammee, W.; Phetcharaburanin, J.; Iamsaard, S.; Tanphaichitr, N. Rats Orally Administered with Ethyl Alcohol for a Prolonged Time Show Histopathology of the Epididymis and Seminal Vesicle Together with Changes in the Luminal Metabolite Composition. Biomedicines2024, 12, 1010.
Taoto, C.; Tangsrisakda, N.; Thukhammee, W.; Phetcharaburanin, J.; Iamsaard, S.; Tanphaichitr, N. Rats Orally Administered with Ethyl Alcohol for a Prolonged Time Show Histopathology of the Epididymis and Seminal Vesicle Together with Changes in the Luminal Metabolite Composition. Biomedicines 2024, 12, 1010.
Abstract
Prolonged ethanol (EtOH) consumption is associated with male infertility with a decreased spermatogenesis rate as one cause. Defective maturation and development of sperm during their storage in the cauda epididymis and transit in the seminal vesicle can be another cause, possibly occurring before the drastic spermatogenesis disruption. Herein, we demonstrated that the cauda epididymis and seminal vesicle of rats, orally fed with EtOH under a regimen that spermatogenesis was still ongoing, showed histological damage, including lesion and decreased height of the epithelial cells, and increased collagen fibers in the muscle layer, which implicated fibrosis. Lipid peroxidation (shown by malondialdehyde (MDA) levels) was observed, indicating that reactive oxygen species (ROS) was produced along with acetaldehyde during EtOH metabolism by CYP2E1. MDA, acetaldehyde and other lipid peroxidation products could further damage cellular components of the cauda epididymis and seminal vesicle and this was supported by increased apoptosis (shown by TUNEL assay and caspase 9/caspase 3 expression) in these two tissues of EtOH-treated rats. Consequently, functionality of the cauda epididymis and seminal vesicle in EtOH-treated rats was impaired, as demonstrated by decreases in 1H NMR-analyzed metabolites (e.g., carnitine, fructose), which were important for sperm development, metabolism and survival in their lumen.
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