鸡的性别逆转与芳香化酶。

Séverine Vaillant, M. Dorizzi, C. Pieau, N. Richard-Mercier
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引用次数: 112

摘要

在性腺分化前施用芳香酶抑制剂可诱导母鸡性别逆转。为了分析性别逆转的过程,我们对非甾体芳香酶抑制剂Fadrozole在性腺芳香酶活性和女性生殖系统形态和结构方面的变化进行了几个月的跟踪研究。在孵化第4天将法唑注射到卵中,并在胚胎发育期间和孵化后8个月观察其效果。对照雌虫的左右性腺芳香化酶活性在胚胎发育的中间三分之一阶段较高,在孵化前逐渐降低。孵化后,左侧卵巢的芳香酶活性增加,特别是在卵泡发育期间,而右侧退行性腺的芳香酶活性继续下降,直到一个月时达到睾丸水平。在接受治疗的女性中,生殖系统的男性化表现为右侧性腺的维持及其分化为睾丸,左侧性腺分化为卵睾丸或睾丸;然而,在所有个体中,左腰勒氏管和右腰勒氏管后部都被保留。在睾丸和卵泡中,芳香化酶活性低于对照雌虫的性腺(除了在孵化后一个月的右侧性腺),但仍高于对照和处理雄虫的睾丸。此外,在卵泡中,有卵泡部分的芳香酶活性高于无卵泡部分。性腺结构变化主要表现为左侧性腺皮质部分(卵睾)或完全(睾丸)变性,两侧性腺形成白蛋白和睾丸索/管分化。睾丸索/管与卵巢髓索和腔隙发生转分化,其上皮增厚并呈粘液样。转分化发生在胚胎和出生后发育的整个过程中;因此,新的睾丸索/管不断形成,而其他的则退化。性腺性别逆转还表现为纤维间质组织丰富,淋巴样细胞髓质凝聚异常;在持续存在的睾丸索/管中,精子发生延迟和受损。与芳香化酶活性相关,持续过高水平的雌激素可以解释性别逆转女性中输卵管、性腺异常和不孕的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex reversal and aromatase in chicken.
Aromatase inhibitors administered before sexual differentiation of the gonads can induce sex reversal in female chickens. To analyze the process of sex reversal, we have followed for several months the changes induced by Fadrozole, a nonsteroidal aromatase inhibitor, in gonadal aromatase activity and in morphology and structure of the female genital system. Fadrozole was injected into eggs on day four of incubation, and its effects were examined during the embryonic development and for eight months after hatching. In control females, aromatase activity in the right and the left gonad was high in the middle third of embryonic development, and then decreased up to hatching. After hatching, aromatase activity increased in the left ovary, in particular during folliculogenesis, whereas in the right regressing gonad, it continued to decrease to reach testicular levels at one month. In treated females, masculinization of the genital system was characterized by the maintenance of the right gonad and its differentiation into a testis, and by the differentiation of the left gonad into an ovotestis or a testis; however, in all individuals, the left Müllerian duct and the posterior part of the right Müllerian duct were maintained. In testes and ovotestes, aromatase activity was lower than in gonads of control females (except in the right gonad as of one month after hatching) but remained higher than in testes of control and treated males. Moreover, in ovotestes, aromatase activity was higher in parts displaying follicles than in parts devoid of follicles. The main structural changes in the gonads during sex reversal were partial (in ovotestes) or complete (in testes) degeneration of the cortex in the left gonad, and formation of an albuginea and differentiation of testicular cords/tubes in the two gonads. Testicular cords/tubes transdifferentiated from ovarian medullary cords and lacunae whose epithelium thickened and became Sertolian. Transdifferentiation occurred all along embryonic and postnatal development; thus, new testicular cords/tubes were continuously formed while others degenerated. The sex reversed gonads were also characterized by an abundant fibrous interstitial tissue and abnormal medullary condensations of lymphoid-like cells; in the persisting testicular cords/tubes, spermatogenesis was delayed and impaired. Related to aromatase activity, persistence of too high levels of estrogens can explain the presence of oviducts, gonadal abnormalities and infertility in sex reversed females.
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