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节律性、相互作用的胃饥饿素和瘦素信号传导:肥胖症发展的新见解

Rhythmic, reciprocal ghrelin and leptin signaling: new insight in the development of obesity.

作者信息

Kalra Satya P, Bagnasco Michela, Otukonyong Effiong E, Dube Michael G, Kalra Pushpa S

机构信息

Department of Neuroscience, College of Medicine, University of Florida McKnight Brain Institute, PO Box 100244, Gainesville, FL 32610-0244, USA.

出版信息

Regul Pept. 2003 Mar 28;111(1-3):1-11. doi: 10.1016/s0167-0115(02)00305-1.

Abstract

The hypothalamus integrates metabolic, neural and hormonal signals to evoke an intermittent appetitive drive in the daily management of energy homeostasis. Three major players identified recently in the feedback communication between the periphery and hypothalamus are leptin, ghrelin and neuropeptide Y (NPY). We propose that reciprocal circadian and ultradian rhythmicities in the afferent humoral signals, anorexigenic leptin from adipocytes and orexigenic ghrelin from stomach, encode a corresponding discharge pattern in the appetite-stimulating neuropeptide Y network in the hypothalamus. An exquisitely intricate temporal relationship among these signaling modalities with varied sites of origin is paramount in sustenance of weight control on a daily basis. Our model envisages that subtle and progressive derangements in temporal communication, imposed by environmental shifts in energy intake, impel a positive energy balance culminating in excessive weight gain and obesity. This conceptual advance provides a new target for designing pharmacologic or gene transfer therapies that would normalize the rhythmic patterns of afferent hormonal and efferent neurochemical messages.

摘要

下丘脑整合代谢、神经和激素信号,在能量平衡的日常管理中引发间歇性的食欲驱动。最近在外周与下丘脑之间的反馈通讯中确定的三个主要参与者是瘦素、胃饥饿素和神经肽Y(NPY)。我们提出,传入体液信号中的昼夜节律和超日节律,即来自脂肪细胞的厌食性瘦素和来自胃的促食欲胃饥饿素,在下丘脑刺激食欲的神经肽Y网络中编码相应的放电模式。这些起源部位不同的信号传导方式之间极其复杂的时间关系,对于日常体重控制的维持至关重要。我们的模型设想,能量摄入的环境变化导致的时间通讯中的细微渐进性紊乱,会促使能量正平衡,最终导致体重过度增加和肥胖。这一概念进展为设计药理或基因转移疗法提供了一个新靶点,这些疗法将使传入激素和传出神经化学信息的节律模式正常化。

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