强迫性进食中的多巴胺D2受体及其下游信号传导。

IF 2.8 3区 医学 Q3 NEUROSCIENCES
Caden Leung, Kabirullah Lutfy
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引用次数: 0

摘要

肥胖已经成为一个重大的公共卫生危机,并成为其他慢性代谢疾病的潜在条件。中脑边缘多巴胺系统的抑制和调节机制失调,特别是多巴胺D2受体(D2Rs),在驱动过度饮食和强迫饮食习惯中起着至关重要的作用。根据目前的文献,长期食用高脂肪食物会引起享乐感,并有可能下调和脱敏D2Rs,损害其信号传导和抑制作用。因此,这种损伤改变了D2Rs的下游信号传导,包括抑制腺苷酸环化酶和相关的级联反应。虽然已经研究了这一途径的各个组成部分,但尚未建立全面的合成。本文旨在探讨D2R下调与脱敏的关系及其对下游信号级联的影响。我们假设这一通路的改变可能导致厌氧神经肽表达失调,从而导致暴饮暴食行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dopamine D2 Receptors and Its Downstream Signaling in Compulsive Eating.

Obesity has become a major public health crisis and serves as an underlying condition for other chronic metabolic diseases. The dysregulation of the inhibitory and regulatory mechanisms of the mesolimbic dopamine system, particularly dopamine D2 receptors (D2Rs), plays a critical role in driving excessive food consumption and compulsive eating habits. Based on the current literature, chronic consumption of high-fat foods elicits hedonic sensations and has the potential to downregulate and desensitize D2Rs, impairing their signaling and inhibitory action. This impairment thereby alters the downstream signaling of the D2Rs, involving the inhibition of adenylyl cyclase and the associated cascade. Although individual components of this proposed pathway have been studied, a comprehensive synthesis has not been established. This review aims to explore the relationship between D2R downregulation and desensitization and their effects on the downstream signaling cascade. We hypothesize that alterations in this pathway may lead to the dysregulation of the expression of orexigenic and anorexigenic neuropeptides, contributing to binge-eating behaviors.

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来源期刊
Brain Sciences
Brain Sciences Neuroscience-General Neuroscience
CiteScore
4.80
自引率
9.10%
发文量
1472
审稿时长
18.71 days
期刊介绍: Brain Sciences (ISSN 2076-3425) is a peer-reviewed scientific journal that publishes original articles, critical reviews, research notes and short communications in the areas of cognitive neuroscience, developmental neuroscience, molecular and cellular neuroscience, neural engineering, neuroimaging, neurolinguistics, neuropathy, systems neuroscience, and theoretical and computational neuroscience. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
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