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甲状腺激素给药对青春期前大鼠支持细胞雄激素代谢影响的随访研究。

Follow-up study on the effects of thyroid hormone administration on androgen metabolism of peripubertal rat Sertoli cells.

作者信息

Panno M L, Salerno M, Lanzino M, De Luca G, Maggiolini M, Straface S V, Prati M, Palmero S, Bolla E, Fugassa E, Andò S

机构信息

Dipartimento di Biologia Cellulare, Università degli Studi della Calabria, Cosenza, Italy.

出版信息

Eur J Endocrinol. 1995 Feb;132(2):236-41. doi: 10.1530/eje.0.1320236.

Abstract

The inhibitory effect of triiodothyronine (T3) given in early postnatal life on Sertoli cell proliferative activity, leading to their precocious terminal differentiation, has been demonstrated previously. However, data concerning the role of thyroid hormone on androgen metabolism of Sertoli cells during the same period are still lacking. In this study we performed a time-course investigation on the effects of T3 treatment on testosterone metabolism in Sertoli cells isolated from 2-, 3- and 4-weeks-old euthyroid rats. Triiodothyronine (3 micrograms/100 g body wt) was given ip., during the last week prior to sacrifice. Sertoli cells from all animal groups initially were cultured under basal conditions during the first 24 h and subsequently in the presence of testosterone (0.5 mumol/l) with or without T3 (1 nmol/l) for an additional 24 h. This treatment given to 2-week-old animals resulted in reduced testicular growth. As far as androgen metabolism is concerned, T3 in vivo and in vitro treatment in 2- and 3-week-old animals induced a lowering of dihydrotestosterone + 3 alpha-diol with an enhancement of the two other 5 alpha-reduced androgens. The effect was much less pronounced in the oldest group. In both 2- and 3-week-old treated rats a marked reduction of oestradiol was observed, which indicates an inhibition of aromatase activity, mainly in younger animals. This enzyme has been reported to be extremely active in Sertoli cells of rats (of the same strain) between the age of 5 and 20 days, but it decreases rapidly thereafter.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

出生后早期给予三碘甲状腺原氨酸(T3)对支持细胞增殖活性具有抑制作用,可导致其过早终末分化,这一点此前已得到证实。然而,关于同一时期甲状腺激素对支持细胞雄激素代谢作用的数据仍然缺乏。在本研究中,我们对T3处理对从2周龄、3周龄和4周龄甲状腺功能正常的大鼠分离出的支持细胞中睾酮代谢的影响进行了一项时间进程研究。在处死前的最后一周,腹腔注射三碘甲状腺原氨酸(3微克/100克体重)。所有动物组的支持细胞最初在基础条件下培养24小时,随后在存在或不存在T3(1纳摩尔/升)的情况下,于睾酮(0.5微摩尔/升)中再培养24小时。对2周龄动物进行这种处理导致睾丸生长减缓。就雄激素代谢而言,2周龄和3周龄动物体内和体外给予T3均导致二氢睾酮+3α -二醇降低,同时另外两种5α -还原雄激素增加。在最年长的组中,这种作用不太明显。在2周龄和3周龄接受处理的大鼠中均观察到雌二醇显著降低,这表明芳香化酶活性受到抑制,主要在较年幼的动物中。据报道,这种酶在5至20日龄大鼠(同一品系)的支持细胞中极其活跃,但此后迅速下降。(摘要截短于250字)

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