棉酚与甲基睾酮和炔雌醇对大鼠精原干细胞分化无影响。

G Cui, W Zheng, Y Sun, Q Zhang, X Deng, X Chen
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引用次数: 0

摘要

本研究旨在探讨棉酚(12mg /kg/d)联合甲基睾酮(20mg /kg/d)和炔雌醇(100 mg/kg/d)长期24周是否会影响大鼠精原干细胞的存在和分化。通过tdt介导的dUTP缺口末端标记检测、精原干细胞移植和生育恢复评估来评估这一点。结果显示,对照组正常大鼠睾丸均出现自发凋亡,凋亡指数(AI)平均为10.24+/-1.52。在方案治疗组中,主要凋亡细胞是精母细胞和精小管中的精子细胞。精原细胞无凋亡(AI平均113.42+/-13.24)。将治疗组大鼠分离的精原干细胞移植到受体裸鼠体内2 ~ 3个月后,在受体裸鼠的精管中发现了细长的大鼠精细胞。停药6周后,与对照组相比,给药组大鼠生育能力恢复。治疗组雌鼠产仔数平均为9.88+/-0.166,对照组为10.30+/-0.171,第一代产仔数基本正常。这些结果表明,给药不影响给药大鼠精原干细胞的存在和分化潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gossypol with methyltestosterone and ethinylestradiol male does not affect rat spermatogonial stem cell differentiation.

The purpose of this study was to investigate whether administration of the regimen of gossypol at 12 mg/kg/day combined with methyltestosterone at 20 mg/kg/day and ethinylestradiol at 100 microg/kg/day for a long term of twenty-four weeks could affect the existence and differentiation of rat spermatogonial stem cell. This was assessed by conducting TdT-mediated dUTP nick end-labeling detection, spermatogonial stem cell transplantation and fertility recovery evaluation. Our results showed that spontaneous apoptosis was observed in normal rats' testes from the control group with an apoptotic index (AI) average of 10.24+/-1.52. In the regimen-treated group, the predominant apoptotic cells were spermatocytes and spermatids in the seminiferous tubules. Spermatogonia were not apoptotic (AI averaged 113.42+/-13.24). Two to three months after transplantation of spermatogonial stem cells isolated from regimen-treated rats into recipient nude mice, elongated rat spermatids were identified in the seminiferous tubules of recipient nude mice. Six weeks after withdrawal of the administration, fertility of the regimen-treated rats was recovered compared with that of the control group. The number of litters produced by females mated with regimen-treated males averaged 9.88+/-0.166 matched 10.30+/-0.171 of control group and the litters of the first generation appeared to be normal. These results indicated that the administration of this regimen did not affect the existence and differentiation potential of spermatogonial stem cells of the regimen-treated rats.

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