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促性腺激素释放激素作为垂体外部位的旁分泌激素和神经递质。

Gonadotropin-releasing hormone as a paracrine hormone and neurotransmitter in extra-pituitary sites.

作者信息

Hsueh A J, Schaeffer J M

出版信息

J Steroid Biochem. 1985 Nov;23(5B):757-64. doi: 10.1016/s0022-4731(85)80011-x.

DOI:10.1016/s0022-4731(85)80011-x
PMID:2867249
Abstract

Gonadotropin-releasing hormone (GnRH), in addition to its classical releasing action at the pituitary level, acts on multiple extrapituitary sites to regulate various reproductive functions. In the rat ovary, specific high affinity GnRH receptors have been identified in granulosa and theca cells. These binding sites mediate the inhibitory effects of GnRH and its agonists on gonadotropin-stimulated estrogen, progestin and androgen biosynthesis. At the granulose cell level, GnRH treatment decreases aromatase activity as well as the biosynthesis of pregnenolone and progesterone via inhibition of cholesterol side-chain cleavage and 3 beta-hydroxysteroid dehydrogenase enzymes. High concentrations of GnRH also stimulate low but significant levels of various steroids. In addition, treatment with high concentrations of GnRH induces ovulation and oocyte maturation in hypophysectomized rats. This is associated with the ability of GnRH to stimulate plasminogen activator activity in cultured granulosa cells. In the rat testis, GnRH receptors have been identified in Leydig but not Sertoli cells. Treatment with GnRH inhibits gonadotropin-stimulated androgen biosynthesis by the cultured Leydig cells. The inhibitory effect of GnRH on testicular androgen production occurs at sites distal to the formation of cyclic AMP and pregnenolone and may be due to decreases in the activity of the enzyme 17 alpha-hydroxylase and 17-20 desmolase. Since hypothalamic GnRH is unlikely to act at the gonadal level, several laboratories have attempted to isolate gonadal GnRH-like peptide which may serve as the ligand for specific gonadal GnRH receptors. Although the presence of ovarian GnRH-like substance still remains elusive, testicular GnRH-like substance has been identified. This gonadal peptide(s) may be an important local paracrine hormone. In addition to its action at the gonadal level, GnRH or GnRH-like peptides may play an important role as a neurotransmitter in the central nervous system. Exogenous administration of GnRH in selected brain areas has been shown to modulate sexual behavior in experimental animals, while neural pathways containing GnRH-like immunoreactive substances have been identified in several brain areas. We have recently synthesized a bioluminescent GnRH analog capable of serving as a specific GnRH ligand for a bioluminescent ligand receptor assay which is more sensitive than classical 125I-ligand assays. We have identified GnRH receptors in small, discrete brain regions. Thus, GnRH and GnRH-like peptides may play important paracrine and neurotransmitter roles in the regulation of various reproductive functions in extra-pituitary sites.

摘要

促性腺激素释放激素(GnRH),除了在垂体水平具有经典的释放作用外,还作用于多个垂体外位点以调节各种生殖功能。在大鼠卵巢中,已在颗粒细胞和卵泡膜细胞中鉴定出特异性高亲和力GnRH受体。这些结合位点介导GnRH及其激动剂对促性腺激素刺激的雌激素、孕激素和雄激素生物合成的抑制作用。在颗粒细胞水平,GnRH处理通过抑制胆固醇侧链裂解酶和3β-羟基类固醇脱氢酶来降低芳香化酶活性以及孕烯醇酮和孕酮的生物合成。高浓度的GnRH也刺激各种类固醇的低但显著水平。此外,用高浓度的GnRH处理可诱导去垂体大鼠排卵和卵母细胞成熟。这与GnRH刺激培养的颗粒细胞中纤溶酶原激活剂活性的能力有关。在大鼠睾丸中,已在睾丸间质细胞而非支持细胞中鉴定出GnRH受体。用GnRH处理可抑制培养的睾丸间质细胞中促性腺激素刺激的雄激素生物合成。GnRH对睾丸雄激素产生的抑制作用发生在环磷酸腺苷和孕烯醇酮形成的远端位点,可能是由于17α-羟化酶和17-20碳链裂解酶活性降低所致。由于下丘脑GnRH不太可能在性腺水平起作用,几个实验室已尝试分离可能作为特异性性腺GnRH受体配体的性腺GnRH样肽。尽管卵巢GnRH样物质的存在仍然难以捉摸,但睾丸GnRH样物质已被鉴定出来。这种性腺肽可能是一种重要的局部旁分泌激素。除了在性腺水平的作用外,GnRH或GnRH样肽可能作为中枢神经系统中的神经递质发挥重要作用。在选定的脑区外源性给予GnRH已被证明可调节实验动物的性行为,而在几个脑区已鉴定出含有GnRH样免疫反应物质的神经通路。我们最近合成了一种生物发光GnRH类似物,它能够作为生物发光配体受体测定的特异性GnRH配体,该测定比经典的125I配体测定更敏感。我们已在小的离散脑区中鉴定出GnRH受体。因此,GnRH和GnRH样肽可能在垂体外位点调节各种生殖功能中发挥重要的旁分泌和神经递质作用。

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