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孕期暴露于乙炔雌二醇所致小鼠性腺发育不全。

Gonadal dysgenesis induced by prenatal exposure to ethinyl estradiol in mice.

作者信息

Yasuda Y, Kihara T, Tanimura T, Nishimura H

出版信息

Teratology. 1985 Oct;32(2):219-27. doi: 10.1002/tera.1420320210.

Abstract

Daily oral administration of ethinyl estradiol (0.02, 0.2, or 2.0 mg/kg of body weight) to pregnant Jc1:ICR mice resulted in ovotestis and intra-abdominal testis with persistent Müllerian duct and Wolffian duct in male fetuses and ovarian hypoplasia in female fetuses when it was given from day 11 through day 17 of gestation (before gonadal differentiation in the fetus). The ovotestis consisted of testicular and ovarian portions. In the testicular portion, a few solid seminiferous tubules containing spermatogonia, some with pachytene nuclei with Sertoli cells and compact interstitial tissue including Leydig cells, were seen. In the ovarian portion, pachytene nuclei were seen. The intra-abdominal testis was smaller and contained more spermatogonia per tubule in cross section than the control testis. These findings suggest that in male fetuses ethinyl estradiol affects Sertoli cell differentiation resulting in suppression of Müllerian inhibiting factor. On the other hand, in the ovarian hypoplasia, the primordial follicles and follicular cells in a primordial follicle were significantly decreased in number, and the number of the degenerated primordial follicles was significantly increased. It seems likely that ethinyl estradiol affects the intimate contact between follicular cells and oocytes to cause degeneration of primordial follicles.

摘要

在妊娠第11天至第17天(胎儿性腺分化之前),每天给怀孕的Jc1:ICR小鼠口服乙炔雌二醇(0.02、0.2或2.0毫克/千克体重),结果导致雄性胎儿出现卵睾和腹腔内睾丸,伴有中肾旁管和中肾管持续存在,雌性胎儿出现卵巢发育不全。卵睾由睾丸和卵巢部分组成。在睾丸部分,可以看到一些含有精原细胞的实性生精小管,有些精原细胞处于粗线期核,伴有支持细胞,还有包括间质细胞的致密间质组织。在卵巢部分,可以看到粗线期核。腹腔内睾丸比对照睾丸小,横切面上每个小管中的精原细胞更多。这些发现表明,在雄性胎儿中,乙炔雌二醇影响支持细胞分化,导致中肾旁管抑制因子受到抑制。另一方面,在卵巢发育不全中,原始卵泡和原始卵泡中的卵泡细胞数量显著减少,退化的原始卵泡数量显著增加。乙炔雌二醇似乎影响卵泡细胞与卵母细胞之间的紧密接触,导致原始卵泡退化。

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