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Ghrelin and glucose homeostasis.

机译:生长激素释放肽和葡萄糖稳态。

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Ghrelin plays an important physiological role in modulating GH secretion, insulin secretion and glucose metabolism. Ghrelin has direct effects on pancreatic islet function. Also, ghrelin is part of a mechanism that integrates the physiological response to fasting. However, pharmacologic studies indicate the important obesogenic/diabetogenic properties of ghrelin. This is very likely of physiological relevance, deriving from a requirement to protect against seasonal periods of food scarcity by building energy reserves, predominantly in the form of fat. Available data indicate the potential of ghrelin blockade as a means to prevent its diabetogenic effects. Several studies indicate a negative correlation between ghrelin levels and the incidence of type 2 diabetes and insulin resistance. However, it is unclear if low ghrelin levels are a risk factor or a compensatory response. Direct antagonism of the receptor does not always have the desired effects, however, since it can cause increased body weight gain. Pharmacological suppression of the ghrelin/des-acyl ghrelin ratio by treatment with des-acyl ghrelin may also be a viable alternative approach which appears to improve insulin sensitivity. A promising recently developed approach appears to be through the blockade of GOAT activity, although the longer term effects of this treatment remain to be investigated.
机译:Ghrelin在调节GH分泌,胰岛素分泌和葡萄糖代谢中起重要的生理作用。 Ghrelin对胰腺胰岛功能有直接影响。另外,生长素释放肽是整合对禁食的生理反应的机制的一部分。但是,药理研究表明,生长素释放肽具有重要的致肥胖/致糖尿病特性。这很可能与生理相关,这源于通过建立主要以脂肪形式的能量储备来防止季节性食物短缺的需求。现有数据表明,ghrelin阻断有可能作为预防其促糖尿病作用的手段。多项研究表明,生长素释放肽水平与2型糖尿病和胰岛素抵抗的发生率呈负相关。然而,目前还不清楚低的生长激素释放肽水平是否是危险因素或代偿性反应。然而,受体的直接拮抗作用并不总是具有所需的作用,因为它可以引起体重增加。通过用去酰基生长素释放肽治疗来抑制生长素释放肽/去酰基生长素释放肽比例的药理学抑制也可能是可行的替代方法,其似乎改善了胰岛素敏感性。尽管该治疗方法的长期作用尚待研究,但似乎有希望通过抑制GOAT活性来开发一种有前途的新方法。

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