Habibi H R, Peter R E, Nahorniak C S, Milton R C, Millar R P
Department of Biological Sciences, University of Calgary, Canada.
Regul Pept. 1992 Feb 18;37(3):271-84. doi: 10.1016/0167-0115(92)90620-a.
All non-mammalian vertebrates as well as marsupial mammals have two or more forms of gonadotropin-releasing hormone (GnRH) in the brain. Goldfish brain and pituitary contains two molecular forms of GnRH, salmon GnRH ([Trp7, Leu8]m-GnRH; s-GnRH) and chicken GnRH-II ([His5, Trp7, Tyr8]m-GnRH; cII-GnRH). Both sGnRH and cII-GnRH stimulate gonadotropin (GtH) as well as growth hormone (GH) release from the goldfish pituitary. The purpose of the present study was to study the activity of the five known forms of GnRHs as well as analogs of mammalian GnRH (m-GnRH) with variant amino acid residues in positions 5, 7 and 8 in terms of binding to GnRH receptors, and release of GTH and GH from the perifused fragments of goldfish pituitary in vitro. All five vertebrate GnRH peptides stimulated both GtH and GH release in a dose-dependent manner, although their potencies were very different. cII-GnRH was somewhat more active than s-GnRH in releasing GtH, whereas s-GnRH tended to have a greater potency than cII-GnRH in terms of GH release. Both chicken GnRH-I (cI-GnRH) and lamprey GnRH (l-GnRH) were significantly less potent than mGnRH, s-GnRH and cII-GnRH in releasing GtH and GH. cII-GnRH binds with higher affinity for the high affinity binding sites compared to all other native peptides. The activity of [Trp7]-GnRH was similar to both s-GnRH and cII-GnRH in releasing GtH and GH. Substitution of His5 resulted in a significant decrease in GtH releasing potencies compared to mGnRH, sGnRH and cII-GnRH. [His5]-GnRH also had lower GH releasing potency than mGnRH and sGnRH. Tyr8, His8 and Leu8 substitutions caused significant decreases in GtH releasing potencies compared to mGnRH, s-GnRH and cII-GnRH, but did not cause a significant change in GH releasing potency. The combination of [His5, Trp7]-GnRH had GtH and GH releasing activities similar to m-GnRH, s-GnRH and cII-GnRH.(ABSTRACT TRUNCATED AT 400 WORDS)
所有非哺乳类脊椎动物以及有袋类哺乳动物的大脑中都有两种或更多形式的促性腺激素释放激素(GnRH)。金鱼的大脑和垂体含有两种分子形式的GnRH,即鲑鱼GnRH([Trp7, Leu8]m - GnRH;s - GnRH)和鸡GnRH - II([His5, Trp7, Tyr8]m - GnRH;cII - GnRH)。sGnRH和cII - GnRH都能刺激金鱼垂体释放促性腺激素(GtH)以及生长激素(GH)。本研究的目的是研究五种已知形式的GnRH以及在第5、7和8位具有不同氨基酸残基的哺乳动物GnRH(m - GnRH)类似物在与GnRH受体结合方面的活性,以及它们在体外对金鱼垂体灌流片段释放GTH和GH的影响。所有五种脊椎动物GnRH肽都以剂量依赖性方式刺激GtH和GH的释放,尽管它们的效力差异很大。在释放GtH方面,cII - GnRH比s - GnRH略活跃,而在释放GH方面,s - GnRH的效力往往比cII - GnRH更强。鸡GnRH - I(cI - GnRH)和七鳃鳗GnRH(l - GnRH)在释放GtH和GH方面的效力明显低于mGnRH、s - GnRH和cII - GnRH。与所有其他天然肽相比,cII - GnRH与高亲和力结合位点的结合亲和力更高。[Trp7] - GnRH在释放GtH和GH方面的活性与s - GnRH和cII - GnRH相似。与mGnRH、sGnRH和cII - GnRH相比,His5的取代导致GtH释放效力显著降低。[His5] - GnRH的GH释放效力也低于mGnRH和sGnRH。与mGnRH、s - GnRH和cII - GnRH相比,Tyr8、His8和Leu8的取代导致GtH释放效力显著降低,但在GH释放效力方面没有引起显著变化。[His5, Trp7] - GnRH的GtH和GH释放活性与m - GnRH、s - GnRH和cII - GnRH相似。(摘要截断于400字)