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Aqueous fruit extract of Mimusops elengi causes reversible suppression of spermatogenesis and fertility in male mice

机译:Mimusops elengi的水果提取物可逆抑制雄性小鼠的精子发生和生育能力

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摘要

Antifertility efficacy of oral administration of aqueous fruit extract of Mimusops elengi (200, 400 and 600mgkg(-1) body weight/day for 35days) was evaluated in Parkes strain male mice. Various reproductive end points such as histopathology, sperm parameters, testosterone level, haematology, serum biochemistry and fertility indices were assessed; activities of 3- and 17-hydroxysteroid dehydrogenases, and immunoblot expressions of StAR and P450scc in the testis were also assessed. Histologically, testes in Mimusops-treated mice showed nonuniform and diverse degenerative changes in the seminiferous tubules; both affected and normal tubules were observed in the same sections of testis. The treatment had adverse effects on testicular hydroxysteroid dehydrogenases and StAR and P450scc, serum level of testosterone and on motility, viability and number of spermatozoa in cauda epididymis. However, serum levels of alanine aminotransferase, aspartate aminotransferase and creatinine, and haematological parameters were not affected by the treatment. Also, libido was not affected in treated males, but their fertility was markedly suppressed. By 56days of treatment withdrawal, the alterations caused in the above parameters recovered to control levels, suggesting that Mimusops treatment causes reversible suppression of spermatogenesis and fertility in Parkes mice. Further, there were no detectable signs of toxicity in treated males.
机译:在Parkes品系雄性小鼠中评估了口服Mimusops elengi的水性水果提取物(200、400和600mgkg(-1)体重/天,共35天)的抗生育功效。评估了各种生殖终点,例如组织病理学,精子参数,睾丸激素水平,血液学,血清生化指标和生育指数。还评估了3-和17-羟基类固醇脱氢酶的活性,以及​​睾丸中StAR和P450scc的免疫印迹表达。从组织学上看,用Mimusops处理的小鼠的睾丸显示出生精小管的不均匀和多样的变性变化。在睾丸的同一部分观察到了受影响的和正常的肾小管。该治疗对睾丸羟基类固醇脱氢酶和StAR和P450scc,睾丸激素的血清水平以及附睾马尾精子的活力,生存力和精子数量有不利影响。但是,血清丙氨酸转氨酶,天冬氨酸转氨酶和肌酐的水平以及血液学参数不受治疗的影响。同样,性欲受治疗的男性没有受到影响,但其生育能力受到了明显抑制。停药56天后,上述参数引起的改变恢复到控制水平,这表明Mimusops治疗可逆地抑制Parkes小鼠的精子发生和生育能力。此外,在治疗的男性中没有可检测到的毒性迹象。

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