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参与胃饥饿素促食欲作用的中枢机制。

Central mechanisms involved in the orexigenic actions of ghrelin.

机构信息

Department of Physiology, Monash University, Clayton, Victoria 3183, Australia.

出版信息

Peptides. 2011 Nov;32(11):2248-55. doi: 10.1016/j.peptides.2011.05.014. Epub 2011 May 17.

Abstract

Ghrelin is a stomach hormone, secreted into the bloodstream, that initiates food intake by activating NPY/AgRP neurons in the hypothalamic acruate nucleus. This review focuses on recent evidence that details the mechanisms through which ghrelin activate receptors on NPY neurons and downstream signaling within NPY neurons. The downstream signaling involves a novel CaMKK-AMPK-CPT1-UCP2 pathway that enhances mitochondrial efficiency and buffers reactive oxygen species in order to maintain an appropriate firing response in NPY. Recent evidence that shows metabolic status affects ghrelin signaling in NPY is also described. In particular, ghrelin does not activate NPY neurons in diet-induced obese mice and ghrelin does not increase food intake. The potential mechanisms and implications of ghrelin resistance are discussed.

摘要

胃饥饿素是一种胃激素,分泌到血液中,通过激活下丘脑弓状核中的 NPY/AgRP 神经元来启动进食。本综述重点介绍了最近的证据,详细说明了胃饥饿素激活 NPY 神经元上的受体以及 NPY 神经元内下游信号转导的机制。下游信号转导涉及一种新型的 CaMKK-AMPK-CPT1-UCP2 途径,可增强线粒体效率并缓冲活性氧,以维持 NPY 中适当的发射反应。还描述了最近的证据表明代谢状态会影响 NPY 中的胃饥饿素信号。特别是,在饮食诱导的肥胖小鼠中,胃饥饿素不会激活 NPY 神经元,也不会增加食物摄入。讨论了胃饥饿素抵抗的潜在机制和意义。

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