慢性乙醇和曲马多对成年雄性白化大鼠睾丸组织的相互作用:实验生化和组织病理学研究

Ahmed Gad Allaha, Mohamed Hemeda
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引用次数: 0

摘要

背景和目的在世界各地的发展中国家和发达国家,年轻人有喝酒和滥用其他药物的倾向。本研究旨在探讨两种常见滥用物质乙醇和曲马多慢性毒性对成年雄性白化大鼠睾丸功能的生化和组织病理学影响。材料与方法将40只动物平均分为4组:对照组只给予生理盐水,乙醇组给予乙醇[30% (v/v)]口服,剂量为2g /kg,曲马多组皮下给予曲马多60mg /kg,乙醇+曲马多组按上述途径按上述剂量给予乙醇+曲马多,持续60 d。末次给药24小时后处死大鼠,取血样,测定血清睾酮水平。取下睾丸并称重。在睾丸中评估谷胱甘肽、超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶和丙二醛水平和组织学(苏木精和伊红)。结果与对照组相比,各试验组睾丸激素水平、睾丸相对重量、睾丸谷胱甘肽、过氧化氢酶、超氧化物歧化酶和谷胱甘肽过氧化物酶均显著降低。相反,与对照组相比,所有实验组的丙二醛均显著升高。乙醇和/或曲马多的睾丸组织学显示结构畸变,与抗氧化剂消耗和氧化应激一致。结论滥用乙醇和曲马多对男性生殖功能具有类似、附加或协同作用,其作用机制可能是由于乙醇和曲马多对雄性生殖功能的抗氧化防御系统产生影响,导致睾丸组织氧化损伤和结构畸变。
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Chronic ethanol and tramadol interaction on the testicular tissues in adult male Albino rats: an experimental biochemical and histopathological study
Background and aim In the developing and advanced countries across the world, young people have the tendency of consuming alcohol in combination with other abused substances. This study aimed to investigate the biochemical and histopathological effects of chronic toxic effects of two commonly abused substances, ethanol and/or tramadol, on testicular function in adult male Albino rats. Materials and methods Forty animals were equally divided into four groups: control group that received normal saline only, ethanol group that received ethanol [30% (v/v)] orally at a dose of 2 g/kg, tramadol group that received tramadol subcutaneously at a dose of 60 mg/kg, and ethanol+tramadol group that received ethanol+tramadol by the route and at the dose described above for 60 days. Twenty-four hours after the administration of the last dose, rats were sacrificed, blood samples were obtained, and serum testosterone was determined. Testes were harvested and weighed. Glutathione, superoxide dismutase, catalase, glutathione peroxidase, and malondialdehyde levels and histology (hematoxylin and eosin) were evaluated in the testis. Results Testosterone level, relative testicular weights, and testicular glutathione, catalase, superoxide dismutase, and glutathione peroxidase were significantly reduced in all experimental groups compared with controls. Conversely, malondialdehyde was significantly increased in all experimental groups compared with controls. Testicular histology in ethanol and/or tramadol showed structural aberrations that are consistent with antioxidant depletion and oxidative stress. Conclusion Abuse of ethanol and/or tramadol exerted similar, additive, and synergistic, adversely affected the male-reproductive functions, which may be due to the effects on the antioxidant-defense system and caused oxidative tissue injury as well as testicular structural aberrations.
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