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Leptin, the brain and energy homeostasis: From an apparently simple to a highly complex neuronal system

机译:瘦素、大脑和能量稳态:从看似简单到高度复杂的神经元系统

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摘要

Abstract Leptin, produced and secreted by white adipose tissue in tight relationship with adipose mass, informs the brain about the status of the energy stores serving as the main peripheral signal for energy balance regulation through interaction with a multitude of highly interconnected neuronal populations. Most obese patients display resistance to the anorectic effect of the hormone. The present review unravels the multiple levels of complexity that trigger hypothalamic response to leptin with the objective of highlighting those critical hubs that, mainly in the hypothalamic arcuate nucleus, may undergo obesity-induced alterations and create an obstacle to leptin action. Several mechanisms underlying leptin resistance have been proposed, possibly representing useful targets to empower leptin effects. Among these, a special focus is herein dedicated to detail how leptin gains access into the brain and how neuronal plasticity may interfere with leptin function.
机译:摘要 瘦素由白色脂肪组织产生和分泌,与脂肪团密切相关,通过与众多高度互联的神经元群的相互作用,告知大脑能量储存的状态,作为能量平衡调节的主要外周信号。大多数肥胖患者表现出对激素厌食作用的抵抗力。本综述揭示了触发下丘脑对瘦素反应的多个层次的复杂性,目的是强调那些主要在下丘脑弓状核中可能发生肥胖诱导的改变并对瘦素作用造成障碍的关键枢纽。已经提出了几种瘦素耐药的潜在机制,可能代表了增强瘦素作用的有用靶点。其中,本文特别关注瘦素如何进入大脑,以及神经元可塑性如何干扰瘦素功能。

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