Zigman Jeffrey M, Bouret Sebastien G, Andrews Zane B
Departments of Internal Medicine (Divisions of Hypothalamic Research and Endocrinology and Metabolism) and Psychiatry, The University of Texas Southwestern Medical Center, Dallas, TX, 75390-9077, USA.
The Saban Research Institute, Developmental Neuroscience Program, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA 90027, USA; Inserm, Jean-Pierre Aubert Research Center, U1172, University Lille 2, Lille, 59045, France.
Trends Endocrinol Metab. 2016 Jan;27(1):54-63. doi: 10.1016/j.tem.2015.09.010. Epub 2015 Nov 2.
Ghrelin is a metabolic hormone that promotes energy conservation by regulating appetite and energy expenditure. Although some studies suggest that antagonizing ghrelin function attenuates body weight gain and glucose intolerance on a high calorie diet, there is little information about the metabolic actions of ghrelin in the obese state. In this review, we discuss the novel concept of obesity-induced central ghrelin resistance in neural circuits regulating behavior, and impaired ghrelin secretion from the stomach. Interestingly, weight loss restores ghrelin secretion and function, and we hypothesize that ghrelin resistance is a mechanism designed to protect a higher body weight set-point established during times of food availability, to maximize energy reserves during a time of food scarcity.
胃饥饿素是一种代谢激素,通过调节食欲和能量消耗来促进能量储备。尽管一些研究表明,拮抗胃饥饿素功能可减轻高热量饮食引起的体重增加和葡萄糖不耐受,但关于肥胖状态下胃饥饿素的代谢作用的信息却很少。在这篇综述中,我们讨论了肥胖诱导的神经回路中调节行为的中枢胃饥饿素抵抗以及胃饥饿素分泌受损的新概念。有趣的是,体重减轻可恢复胃饥饿素的分泌和功能,我们推测胃饥饿素抵抗是一种机制,旨在保护在食物充足时期建立的较高体重设定点,以便在食物短缺时期最大限度地储备能量。