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食欲素基因与人类行为调节相关表型(包括物质使用)之间的遗传关联。

Genetic associations between orexin genes and phenotypes related to behavioral regulation in humans, including substance use.

作者信息

Aliev Fazil, De Sa Nogueira David, Aston-Jones Gary, Dick Danielle M

机构信息

Department of Psychiatry, Rutgers Robert Wood Johnson Medical School, Piscataway, NJ, 08854, USA.

Rutgers Addiction Research Center, Brain Health Institute, Rutgers University and Rutgers Health, Piscataway, NJ, 08854, USA.

出版信息

Mol Psychiatry. 2025 Jan 29. doi: 10.1038/s41380-025-02895-4.

Abstract

The hypothalamic neuropeptide system of orexin (hypocretin) neurons provides projections throughout the neuraxis and has been linked to sleep regulation, feeding and motivation for salient rewards including drugs of abuse. However, relatively little has been done to examine genes associated with orexin signaling and specific behavioral phenotypes in humans. Here, we tested for association of twenty-seven genes involved in orexin signaling with behavioral phenotypes in humans. We tested the full gene set, functional subsets, and individual genes involved in orexin signaling. Our primary phenotype of interest was Externalizing, a composite factor comprised of behaviors and disorders associated with reward-seeking, motivation, and behavioral regulation. We also tested for association with additional phenotypes that have been related to orexin regulation in model organism studies, including alcohol consumption, problematic alcohol use, daytime sleepiness, insomnia, cigarettes per day, smoking initiation, and body mass index. The composite set of 27 genes corresponding to orexin function was highly associated with Externalizing, as well as with alcohol consumption, insomnia, cigarettes per day, smoking initiation and BMI. In addition, all gene subsets (except the OXR2/HCRTR2 subset) were associated with Externalizing. BMI was significantly associated with all gene subsets. The "validated factors for PPOX/HCRT" and "PPOX/HCRT upregulation" gene subsets also were associated with alcohol consumption. Individually, 8 genes showed a strong association with Externalizing, 12 with BMI, 7 with smoking initiation, 3 with alcohol consumption, and 2 with problematic alcohol use, after correction for multiple testing. This study indicates that orexin genes are associated with multiple behaviors and disorders related to self-regulation in humans. This is consistent with prior work in animals that implicated orexin signaling in motivational activation induced by salient stimuli, and supports the hypothesis that orexin signaling is an important potential therapeutic target for numerous behavioral disorders.

摘要

食欲素(下丘脑泌素)神经元的下丘脑神经肽系统向整个神经轴发出投射,并与睡眠调节、进食以及包括滥用药物在内的显著奖赏动机相关联。然而,在人类中,针对与食欲素信号传导及特定行为表型相关基因的研究相对较少。在此,我们测试了27个参与食欲素信号传导的基因与人类行为表型之间的关联性。我们对整个基因集、功能亚组以及参与食欲素信号传导的单个基因进行了测试。我们感兴趣的主要表型是外化,这是一个由与寻求奖赏、动机及行为调节相关的行为和障碍组成的复合因子。我们还测试了与在模式生物研究中与食欲素调节相关的其他表型的关联性,包括酒精摄入量、酒精使用问题、日间嗜睡、失眠、每日吸烟量、吸烟起始以及体重指数。与食欲素功能相对应的27个基因的复合集与外化以及酒精摄入量、失眠、每日吸烟量、吸烟起始和体重指数高度相关。此外,所有基因亚组(除了OXR2/HCRTR2亚组)均与外化相关。体重指数与所有基因亚组均显著相关。“PPOX/HCRT的验证因子”和“PPOX/HCRT上调”基因亚组也与酒精摄入量相关。在进行多重检验校正后,单个基因方面,8个基因与外化有强关联,12个与体重指数相关,7个与吸烟起始相关,3个与酒精摄入量相关,2个与酒精使用问题相关。这项研究表明,食欲素基因与人类中多种与自我调节相关的行为和障碍有关。这与之前在动物中的研究结果一致,即食欲素信号传导参与了由显著刺激诱导的动机激活,并支持了食欲素信号传导是众多行为障碍重要潜在治疗靶点的假说。

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