短暂性新生儿甲状腺功能减退症促进成年Wistar大鼠睾丸雌二醇合成

N. Venkatesh, M. K. Kumar, S. Sambavi, N. Kalpana, A. M. S. John, J. Anbalagan, R. Ilangovan, M. Aruldhas
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引用次数: 1

摘要

一过性新生儿甲状腺功能减退症可增加成年时的支持细胞(SC)、间质细胞(LC)和生殖细胞(GC)数量。现有的报告将LCs的类固醇生成潜力降低归因于这类大鼠的血清睾酮未改变/降低,尽管细胞数量增加。然而,这些研究忽略了雌二醇在这种情况下的地位。在本研究中,我们验证了“短暂性新生儿甲状腺功能减退可能导致成年大鼠睾丸激素生成向雌二醇生成的时间转移”的假设。从出生后第1天(PND 1)到第14天或从第1天到第29天,通过在饮用水中添加0.05%的甲巯咪唑(MMI)诱导新生儿甲状腺功能减退。试验期结束后,给予不含MMI的饮水,用PND 91处死。未接触MMI的同龄大鼠作为对照。放射免疫分析显示血清促黄体生成素(LH)、促卵泡激素(FSH)、生长激素(GH)和催乳素(PRL)滴度降低;血清睾酮维持不变,但睾丸间质液(TIF)睾酮水平下降。在睾酮的两种主要代谢物中,血清和TIF中5α-二氢睾酮(DHT)浓度下降,而雌二醇在两者中均显著升高。新生儿发作的短暂性甲状腺功能减退降低了LCs中3β-羟基类固醇脱氢酶(3β-HSD)的活性,但增加了17β-HSD的活性。放射受体测定显示,甲状腺功能减退组LHR和ER浓度降低,AR和PRLR浓度升高。与对照大鼠相比,LCs的芳香酶活性下降,而SCs的芳香酶活性随着FSHR的增加而增加。LHR和FSHR水平以及芳香化酶的变化与各自基因的表达水平一致。本研究支持上述假设,并提示新生儿发作性甲状腺功能减退引起的成年大鼠睾丸中一过性雌二醇升高可能是由于这些大鼠sc中芳香化酶的表达和活性以及FSHR含量的增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transient Neonatal-Onset Hypothyroidism Boosts Estradiol Synthesis in the Testis of Adult Wistar Rat
Transient neonatal hypothyroidism is known to boost Sertoli cell (SC), Leydig cell (LC) and germ cell (GC) number at adult age. Existing reports attribute decreased steroidogenic potential of LCs to unaltered/decreased serum testosterone in such rats, despite a boost in the cell number. However, these studies have ignored the status of estradiol in such conditions. In this present study, we tested the hypothesis "transient neonatal-onset hypothyroidism may lead to a temporal shift in adult rat testicular steroidogenesis towards estradiol production". Hypothyroidism was induced in neonates by providing methimazole (MMI) in drinking water (0.05%) to lactating mothers and pups for a transient period from postnatal day 1 (PND 1) to PND 14 or from PND 1 to PND 29. After the experimental period, the pups were provided drinking water free of MMI and sacrificed on PND 91. Coeval rats without MMI exposure served as control. Radioimmunoassay revealed decreased serum titres of luteinizing hormone (LH), follicle stimulating hormone (FSH), growth hormone (GH) and prolactin (PRL); while serum testosterone remained unaltered, its level in testicular interstitial fluid (TIF) decreased. Between the two major metabolites of testosterone, 5α-dihydrotestosterone (DHT) concentration decreased in serum and TIF, whereas estradiol recorded a significant increase in both. Transient neonatal-onset hypothyroidism decreased 3β-hydroxy steroid dehydrogenase (3β-HSD) in LCs but augmented 17β-HSD activity. Radio-receptor assay revealed decreased concentration of LHR and ER in LCs of hypothyroid groups, whereas AR and PRLR increased. While aromatase activity decreased in LCs, it increased along with FSHR in SCs, when compared to control rats. The changes in LHR and FSHR levels and aromatase were consistent with the expression level of the respective genes. The present study supports the proposed hypothesis and suggests that transient neonatal-onset hypothyroidism-induced boost in estradiol in adult rat testis may be due to augmented expression and activity of aromatase, and FSHR content in SCs of these rats.
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