首页> 外文期刊>European Journal of Pharmacology: An International Journal >Novel hexarelin analogs stimulate feeding in the rat through a mechanism not involving growth hormone release.
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Novel hexarelin analogs stimulate feeding in the rat through a mechanism not involving growth hormone release.

机译:新颖的hexarelin类似物通过不涉及生长激素释放的机制刺激大鼠进食。

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摘要

Growth hormone-releasing peptides (GHRPs) are a class of small peptides that stimulate growth hormone (GH) release in several animal species, including the human. Moreover, GHRPs injected into the brain ventricles stimulate feeding in the rat. The aim of this study was to evaluate the GH-releasing properties of a series of novel GHRP analogs and the possible existence of functional correlations between the GH-releasing activity and the effects on feeding behavior. Two well-known hexapeptides, GHRP-6 and hexarelin, given s.c., dose dependently stimulated both GH release and feeding behavior in satiated rats. However, in a series of tri-, penta- and hexapeptide analogs of hexarelin, some compounds were active either on GH release or on eating behavior. Interestingly, even minor structural modifications resulted in major changes of the pharmacological profile. We conclude that GHRPs have orexigenic properties after systemic administration which are largely independent from the effects they exert on GH release.
机译:生长激素释放肽(GHRPs)是一类小肽,可刺激包括人类在内的几种动物体内的生长激素(GH)释放。而且,注入脑室的GHRP刺激了大鼠的进食。这项研究的目的是评估一系列新颖的GHRP类似物的GH释放特性,以及GH释放活性和对喂养行为的影响之间可能存在功能相关性。皮下注射两种众所周知的六肽GHRP-6和hexarelin剂量依赖性地刺激饱足大鼠的GH释放和进食行为。但是,在一系列的hexarelin三肽,五肽和六肽类似物中,某些化合物对GH释放或进食行为具有活性。有趣的是,即使微小的结构修饰也导致药理学特征的重大变化。我们得出的结论是,GHRPs在全身给药后具有致癌性,这在很大程度上与它们对GH释放的作用无关。

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