M Korbonits, J A Little, C Camacho-Hübner, P J Trainer, G M Besser, A B Grossman
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引用次数: 0
摘要
本研究旨在通过体外大鼠下丘脑模型研究胰岛素样生长因子- i (IGF-I)和IGF-II与下丘脑激素生长激素释放激素(GHRH)和生长抑素(SS)之间的反馈回路。IGF- i和较小程度的IGF- ii都激活1型IGF受体,而2型受体仅由IGF- ii激活。IGF-I、IGF-II及其各种特异性类似物(Des[1-3]IGF-I、[Arg54/Arg55]IGF-II和[Leu27]IGF-II)、胰岛素和2型受体拮抗剂β -半乳糖苷酶单独或联合使用,研究其对GHRH和SS释放的影响。我们的研究结果表明,在体外系统中,IGF对GHRH释放的负反馈效应需要同时激活1型和2型IGF受体,这与早期在体内的研究结果一致。任何多肽组合都不会改变生长抑素。
Insulin-like growth factor-I and- II in combination inhibit the release of growth hormone-releasing hormone from the rat hypothalamus in vitro.
This study was designed to investigate the feedback loop between insulin-like growth factor-I (IGF-I) and IGF-II and the hypothalamic hormones growth hormone-releasing hormone (GHRH) and somatostatin (SS) using an in vitro rat hypothalamic model. IGF-I and, to lesser extent, IGF-II, both activate type 1 IGF receptors, while type 2 receptors are activated by IGF-II alone. IGF-I, IGF-II, their various specific analogues (Des[1-3]IGF-I, [Arg54/Arg55]IGF-II and [Leu27]IGF-II), insulin and the type 2 receptor antagonist beta-galactosidase were used on their own or in combination to study their effect on GHRH and SS release. Our results suggest that the simultaneous activation of type 1 and type 2 IGF receptors is needed for the negative feedback effect of IGFs on GHRH release in this in vitro system, in agreement with earlier findings in vivo. Somatostatin was not altered by any combination of peptides.