Identification of specific sites of hormonal regulation in spermatogenesis in rats, monkeys, and man.

R. McLachlan, L. O’Donnell, S. Meachem, P. Stanton, deKretser Dm, K. Pratis, D. Robertson
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引用次数: 437

Abstract

A detailed understanding of the hormonal regulation of spermatogenesis is required for the informed assessment and management of male fertility and, conversely, for the development of safe and reversible male hormonal contraception. An approach to the study of these issues is outlined based on the use of well-defined in vivo models of gonadotropin/androgen deprivation and replacement, the quantitative assessment of germ cell number using stereological techniques, and the directed study of specific steps in spermatogenesis shown to be hormone dependent. Drawing together data from rat, monkey, and human models, we identify differences between species and formulate an overview of the hormonal regulation of spermatogenesis. There is good evidence for both separate and synergistic roles for both testosterone and follicle-stimulating hormone (FSH) in achieving quantitatively normal spermatogenesis. Based on relatively selective withdrawal and replacement studies, FSH has key roles in the progression of type A to B spermatogonia and, in synergy with testosterone, in regulating germ cell viability. Testosterone is an absolute requirement for spermatogenesis. In rats, it has been shown to promote the adhesion of round spermatids to Sertoli cells, without which they are sloughed from the epithelium and spermatid elongation fails. The release of mature elongated spermatids from the testis (spermiation) is also under FSH/testosterone control in rats. Data from monkeys and men treated with steroidal contraceptives indicate that impairment of spermiation is a key to achieving azoospermia. The contribution of 5alpha-reduced androgens in the testis to the regulation of spermatogenesis is also relevant, as 5alpha-reduced androgens are maintained during gonadotropin suppression and may act to maintain low levels of germ cell development. These concepts are also discussed in the context of male hormonal contraceptive development.
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大鼠、猴子和人类精子发生中激素调控的特定位点的鉴定。
对精子发生的激素调节的详细了解,对于男性生育能力的知情评估和管理是必要的,反过来,对于开发安全和可逆的男性激素避孕也是必要的。研究这些问题的方法是基于使用明确定义的促性腺激素/雄激素剥夺和替代的体内模型,使用立体学技术对生殖细胞数量进行定量评估,以及对精子发生中显示依赖激素的特定步骤的定向研究。从大鼠、猴子和人类模型中收集数据,我们确定了物种之间的差异,并概述了精子发生的激素调节。有充分的证据表明,睾酮和促卵泡激素(FSH)在实现定量正常精子发生中的单独和协同作用。基于相对选择性的停药和替代研究,FSH在A型精原细胞向B型精原细胞的进展中起关键作用,并与睾酮协同作用,调节生殖细胞活力。睾丸素是精子形成的绝对需要。在大鼠中,它已被证明可以促进圆形精子细胞与支持细胞的粘附,如果没有这种粘附,它们就会从上皮脱落,精子细胞的延伸就会失败。大鼠睾丸中成熟细长精子的释放(精子)也受到FSH/睾酮的控制。用类固醇避孕药治疗的猴子和男性的数据表明,精子受损是实现无精子症的关键。睾丸中5α -减少的雄激素对精子发生的调节也有作用,因为在促性腺激素抑制期间维持5α -减少的雄激素,并可能维持低水平的生殖细胞发育。这些概念也在男性激素避孕发展的背景下进行了讨论。
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