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MECHANISMS IN ENDOCRINOLOGY: Hormonal regulation of spermatogenesis: mutant mice challenging old paradigms

机译:内分泌机制:精子发生的激素调节:挑战旧范式的突变小鼠

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The two pituitary gonadotrophins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), and in particular LH-stimulated high intratesticular testosterone (ITT) concentration, are considered crucial for spermatogenesis. We have revisited these concepts in genetically modified mice, one being the LH receptor ( R )-knockout mouse (LuRKO), the other a transgenic mouse expressing in Sertoli cells a highly constitutively active mutated Fshr (Fshr-CAM). It was found that full spermatogenesis was induced by exogenous testosterone treatment in LuRKO mice at doses that restored ITT concentration to a level corresponding to the normal circulating testosterone level in WT mice, ≈5?nmol/L, which is 1.4% of the normal high ITT concentration. When hypogonadal LuRKO and Fshr-CAM mice were crossed, the double-mutant mice with strong FSH signaling, but minimal testosterone production, showed near-normal spermatogenesis, even when their residual androgen action was blocked with the strong antiandrogen flutamide. In conclusion, our findings challenge two dogmas of the hormonal regulation of male fertility: (1) high ITT concentration is not necessary for spermatogenesis and (2) strong FSH stimulation can maintain spermatogenesis without testosterone. These findings have clinical relevance for the development of hormonal male contraception and for the treatment of idiopathic oligozoospermia.
机译:黄体生成激素(LH)和促卵泡激素(FSH)这两种垂体促性腺激素,特别是LH刺激的高睾丸内睾丸激素(ITT)浓度,对于精子发生至关重要。我们在转基因小鼠中重新审视了这些概念,一种是LH受体敲除小鼠(LuRKO),另一种是在Sertoli细胞中表达高度组成性活性的Fshr(Fshr-CAM)的转基因小鼠。发现通过外源性睾丸激素治疗在LuRKO小鼠中诱导了完全的精子形成,其剂量可使ITT浓度恢复至与WT小鼠的正常循环睾丸激素水平相对应的水平,≈5?nmol / L,是正常高水平的1.4%。 ITT浓度。当性腺功能低下的LuRKO和Fshr-CAM小鼠杂交时,具有强FSH信号但睾丸激素产生量很少的双突变小鼠表现出接近正常的精子发生,即使其残余的雄激素作用被强的抗雄激素氟他胺阻断。总之,我们的发现挑战了男性生育力激素调节的两个教条:(1)高ITT浓度对于精子发生不是必需的;(2)强烈的FSH刺激可以在没有睾丸激素的情况下维持精子发生。这些发现对荷尔蒙男性避孕的发展和特发性少精子症的治疗具有临床意义。

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