5α-还原酶I型、P450芳香化酶及雄激素和雌激素受体在不同出生龄附睾脂肪切除术小鼠睾丸中的表达变化

Development & reproduction Pub Date : 2024-12-01 Epub Date: 2024-12-31 DOI:10.12717/DR.2024.28.4.153
Yong-Seung Lee, Ki-Ho Lee
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引用次数: 0

摘要

附睾脂肪是维持正常精子发生所必需的,在不同出生年龄的附睾脂肪切除术导致几种睾丸类固醇生成酶的表达模式被破坏。本研究探讨了不同出生年龄附睾脂肪切除术对小鼠睾丸细胞色素5α-还原酶I、细胞色素P450芳香化酶、雄激素受体(AR)、雌激素受体(ER) α和β表达的影响。产后2月龄行附睾脂肪切除术后,细胞色素5α-还原酶I、细胞色素P450芳香化酶、AR、ER α和β表达水平显著升高。然而,在出生后5个月,睾丸中这些基因的表达在附睾脂肪切除术后显著降低。在出生后8个月和12个月进行附睾脂肪切除术对细胞色素5α-还原酶I、细胞色素P450芳香化酶、AR和ER β的表达水平没有影响。然而,在出生后12个月,切除附睾脂肪后,ER α明显降低。这些观察结果表明,受附睾脂肪影响的睾丸中这些基因的表达在出生后早期比在出生后后期更容易受到影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expressional Alternation of 5α-Reductase Type I, P450 Aromatase, and Androgen and Estrogen Receptors in the Mouse Testis Induced by the Lipectomy of the Epididymal Fat at Different Postnatal Ages.

The epididymal fat is required for the maintenance of normal spermatogenesis, and the lipectomy of epididymal fat at different postnatal age results in disrupted expression patterns of several testicular steroidogenic enzymes. The current research examined the effect of epididymal fat lipectomy at different postnatal ages on expression of cytochrome 5α-reductase I, cytochrome P450 aromatase, androgen receptor (AR), and estrogen receptors (ER) α and β in the mouse testis after 2 weeks of the lipectomy. The lipectomy of epididymal fat at 2 months of postnatal age resulted in significant increases of expression levels of cytochrome 5α-reductase I, cytochrome P450 aromatase, AR, and ER α and β. However, expressions of these genes in the testis were significantly decreased by the lipectomy of epididymal fat at 5 months of postnatal age. The lipectomy of epididymal fat at 8 months and 12 months of postnatal ages did not influence expression levels of cytochrome 5α-reductase I, cytochrome P450 aromatase, AR, and ER β. However, a significant decrease of ER α was detected with the lipectomy of epididymal fat at 12 months of postnatal age. These observations suggest that expression of these genes in the testis by the influence of the epididymal fat is more susceptible at the earlier postnatal development than at the later postnatal period.

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