合成代谢雄激素类固醇癸酸诺龙对大鼠附睾水通道蛋白1和9表达的调节。

Development & reproduction Pub Date : 2021-12-01 Epub Date: 2021-12-31 DOI:10.12717/DR.2021.25.4.245
Ki-Ho Lee
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引用次数: 0

摘要

精子在附睾中成熟,附睾分为初始节和头、体、尾。水通过附睾上皮的运动对精子成熟的腔内微环境的创造是重要的。水通道蛋白(Aquaporins, Aqps)是水通道蛋白,其表达受雄激素调控。目前的研究重点是研究雄激素合成代谢类固醇癸酸诺龙(ND)对Aqp1和Aqp9的表达调节。以低剂量(2 mg/ kg体重/周)或高剂量(10 mg)给药雄性大鼠皮下注射2周或12周。通过实时定量聚合酶链反应(PCR)检测Aqp1和Aqp9的转录水平。在初始阶段,高剂量治疗12周后Aqp1水平下降,高剂量治疗12周后Aqp9水平下降。在附睾头,Aqp9的表达在低剂量下降低。治疗2周后,附睾Aqp1水平升高,Aqp9表达降低。在附睾中,低剂量处理12周导致Aqp1和Aqp9水平降低,而高剂量处理导致Aqp1表达升高,Aqp9水平降低。大剂量治疗2周和12周后,附睾尾Aqp1表达降低,大剂量治疗2周和大剂量治疗12周时Aqp9表达升高。这些结果表明ND对附睾各节段Aqp1和Aqp9表达的调控存在差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Expressional Modulation of Aquaporin 1 and 9 in the Rat Epididymis by an Anabolic-Androgenic Steroid, Nandrolone Decanoate.

Expressional Modulation of Aquaporin 1 and 9 in the Rat Epididymis by an Anabolic-Androgenic Steroid, Nandrolone Decanoate.

Expressional Modulation of Aquaporin 1 and 9 in the Rat Epididymis by an Anabolic-Androgenic Steroid, Nandrolone Decanoate.

Expressional Modulation of Aquaporin 1 and 9 in the Rat Epididymis by an Anabolic-Androgenic Steroid, Nandrolone Decanoate.

The spermatozoa become mature in the epididymis which is divided into initial segment and caput, corpus, and cauda epididymis. The water movement across the epididymal epithelium is important for creating luminal microenvironment for sperm maturation. Aquaporins (Aqps) are water channel proteins, and expression of Aqps is regulated by androgens. The current research was focused to examine expressional regulation of Aqp1 and Aqp9 by an androgenic-anabolic steroid, nandrolone decanoate (ND). The ND at the low dose (2 mg/ kg body weight/week) or high dose (10 mg) was subcutaneously administrated into male rats for 2 or 12 weeks. Transcript levels of Aqp1 and Aqp9 were determined by quantitative real-time polymerase chain reaction (PCR) analyses. In the initial segment, level of Aqp1 was decreased with 12 week-treatment, while Aqp9 level was decreased by the high dose treatment for 12 weeks. In the caput epididymis, Aqp9 expression was decreased by the low dose treatment. The 2 week-treatment resulted in an increase of Aqp1 level but a decrease of Aqp9 expression in the corpus epididymis. In the corpus epididymis, the 12 week-treatment at the low dose caused the reduction of Aqp1 and Aqp9 levels, but the high dose treatment resulted in an increase of Aqp1 expression and a decrease of Aqp9 level. In the cauda epididymis, Aqp1 expression was decreased by 2 and 12 week-treatments, while increases of Aqp9 levels was detected with the high dose treatment for 2 weeks and with 12 week-treatment. These findings indicate differential regulation of Aqp1 and Aqp9 expression among epididymal segments by ND.

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