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解丽君, 赵松, 吕胜敏, 胡文媛. 锌对乙醇长期摄入致大鼠睾丸损伤保护作用[J]. 中国公共卫生, 2009, 25(10): 1252-1254. DOI: 10.11847/zgggws2009-25-10-52
引用本文: 解丽君, 赵松, 吕胜敏, 胡文媛. 锌对乙醇长期摄入致大鼠睾丸损伤保护作用[J]. 中国公共卫生, 2009, 25(10): 1252-1254. DOI: 10.11847/zgggws2009-25-10-52
XIE Li-jun, ZHAO Song, . Protective effect of zinc on oxidative injury of testis induced by chronic alcohol exposure in rats[J]. Chinese Journal of Public Health, 2009, 25(10): 1252-1254. DOI: 10.11847/zgggws2009-25-10-52
Citation: XIE Li-jun, ZHAO Song, . Protective effect of zinc on oxidative injury of testis induced by chronic alcohol exposure in rats[J]. Chinese Journal of Public Health, 2009, 25(10): 1252-1254. DOI: 10.11847/zgggws2009-25-10-52

锌对乙醇长期摄入致大鼠睾丸损伤保护作用

Protective effect of zinc on oxidative injury of testis induced by chronic alcohol exposure in rats

  • 摘要: 目的观察锌对乙醇长期摄入所致大鼠睾丸损伤的保护作用机制。方法30只健康雄性成年SD大鼠随机分为对照组、乙醇组、乙醇+葡萄糖酸锌组,各组每日分别灌胃0,7.5g/kg乙醇、7.5g/kg乙醇+7.7mg/kg葡萄糖酸锌,连续13周后检测精子计数、活动率、精子畸形率,血清睾酮;光、电镜观察睾丸的形态改变,同时测定睾丸线粒体中丙二醛(MDA)的产生量,免疫组织化学法和蛋白印迹(western-blot)检测睾丸组织中诱导型一氧化氮合酶(iNOS)的表达。结果与对照组(38.0±7.9)×106/mL比较,乙醇组精子计数为(8.2±5.1)×106/mL,减少了78%(P<0.05),精子活动率下降了71%(P<0.05),精子畸形率明显升高(P<0.05),血清睾酮水平明显降低(P<0.05);睾丸生精上皮结构破坏,支持细胞和各级生精细胞均有退化变性;睾丸生精细胞iNOS表达明显增强(P<0.05);睾丸线粒体丙二醛含量明显升高。乙醇+葡萄糖酸锌组较单纯乙醇组精子计数、精子活动率上升,生精细胞退化变性程度减轻,睾丸生精细胞iNOS表达减弱(P<0.05),睾丸线粒体MDA减少,但血清睾酮仍低于对照组。结论长期摄入乙醇会抑制精子生成和睾酮合成,补充锌可以抑制乙醇引起的睾丸过氧化损伤,保护睾丸的生精功能。

     

    Abstract: ObjectiveTo study testicular structural and functional disturbance induced by chronic alcohol exposure in rats and the protective effect of zinc against the injury.MethodsThirty healthy Sprague-Dawley adult male rats were randomly divided into 3 groups: control, alcohol (7.5g/kg) and alcohol (7.5g/kg)+zinc gluconate (7.7mg/kg).Alcohol and zinc gluconate were administmted to the rats for 13 weeks by gastric tube Speun counting, motility and the percent of abnounal speun were observed Semm sexual hounones(T) were deteun fined The pathological changes of testicle tissue were observed by light and electron microscopy The malonaldehyde (MDA)content of testicular mitochondrial was sinultaneously deteunined.The expression of NOS in testis was detected by inmunohistochemistry and western blot.ResultsCompared with the control group, the speun counting and motility of the alcohol group were decreased (P<0.05);the frequency of abnounal speun was increased(P<0.05);and the seaun T level significantly decreased (P<0.05).The MDA content and the expression of NOS were markedly higher than that of control(P<0.05).Histological evaluation of testis revealed that seminiferous epithelium was disorganized and that sertoli cells and geun cells were degenerated in alcohol-treated rats Zinc supplementation decreased the testicularm itochondrial MDA founation and the expression of NOS in testis and the degeneration of geun cells was inproved Speun counting and motilitywere higher than that of alcohol treated group.But the seaun T level declined.ConclusionChronic alcohol intake leads to speun atogenesis and steroidogenesis inhibition in testis of rats Zinc supplementation inhibits the testicularperoxidation injury.

     

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