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首页> 外文期刊>Neuroendocrinology: International Journal for Basic and Clinical Studies on Neuroendocrine Relationships >Differential orexigenic effects of hexarelin and its analogs in the rat hypothalamus: indication for multiple growth hormone secretagogue receptor subtypes.
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Differential orexigenic effects of hexarelin and its analogs in the rat hypothalamus: indication for multiple growth hormone secretagogue receptor subtypes.

机译:hexarelin及其类似物在大鼠下丘脑中的不同致癌作用:多种生长激素促分泌素受体亚型的指征。

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We have previously reported that hexarelin and some of its analogs, including EP 50885, stimulated GH secretion and feeding after systemic administration in the rat, whereas EP 40904 selectively stimulated food intake and EP 40737 only GH release. The precise mechanism of growth hormone-releasing peptides (GHRPs) actions is still unclear, but the integrity of the arcuate nucleus of the hypothalamus (ARC) appears crucial for their endocrine effects. To better characterize the site(s) and mechanisms(s) of the orexigenic action of GHRPs, we have investigated their effects after infusion into the arcuate, paraventricular, ventromedial and medial preoptic areas of the hypothalamus. Food intake was measured for 60 min following injection of the test compound (2 microg/rat). Hexarelin, EP 40904 and EP 50885 had significant orexigenic effects after injection into the ARC. A specific NPY antagonist significantly inhibited the effect of hexarelin, whereas a GHRH antagonist was ineffective. In the paraventricular nucleus, only EP 50885 stimulated feeding, whereas all peptides were ineffective in the ventromedial nucleus and medial preoptic area. Taken altogether, these results demonstrate that GHRPs are endowed with site-specific orexigenic actions and that endogenous NPY, but not GHRH, mediates these effects. The additional orexigenic action of EP 50885 in the paraventricular nucleus suggests the existence of a GHRP receptor subtype different from the already cloned one. Copyright 2000 S. Karger AG, Basel
机译:先前我们曾报道过,六氯瑞林及其某些类似物(包括EP 50885)在大鼠全身性给药后可刺激GH分泌和喂养,而EP 40904则选择性刺激食物摄入,而EP 40737仅刺激GH释放。尚不清楚生长激素释放肽(GHRPs)作用的确切机制,但下丘脑(ARC)弓形核的完整性对其内分泌作用至关重要。为了更好地表征GHRP的致食作用的部位和机制,我们已经研究了它们注入下丘脑的弓形,室旁,腹膜外和内侧视前区后的作用。注射测试化合物(2微克/大鼠)后60分钟测量食物摄入量。 Hexarelin,EP 40904和EP 50885在注入ARC后具有明显的致癌作用。特定的NPY拮抗剂可显着抑制hexarelin的作用,而GHRH拮抗剂无效。在心室旁核中,只有EP 50885刺激进食,而所有肽在腹侧核和视前内侧区域均无效。总而言之,这些结果表明GHRP具有位点特异性的致病作用,并且内源性NPY而非GHRH介导了这些作用。 EP 50885在心室旁核中的其他致癌作用表明存在与已克隆的人不同的GHRP受体亚型。版权所有2000 S. Karger AG,巴塞尔

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