Cholecystokinin-expressing neurons of the ventromedial hypothalamic nucleus control energy homeostasis.

IF 4.2 3区 医学 Q2 NEUROSCIENCES
Frontiers in Cellular Neuroscience Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.3389/fncel.2024.1483368
Vasileios Eftychidis, Tommas J Ellender, Jacek Szymanski, Liliana Minichiello
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引用次数: 0

Abstract

The hypothalamus is the primary center of the brain that regulates energy homeostasis. The ventromedial hypothalamus (VMH) plays a central role in maintaining energy balance by regulating food intake, energy expenditure, and glucose levels. However, the cellular and molecular mechanisms underlying its functions are still poorly understood. Cholecystokinin (CCK) is one of many genes expressed in this hypothalamic nucleus. Peripheral CCK regulates food intake, body weight, and glucose homeostasis. However, current research does not explain the function of CCK neurons in specific nuclei of the hypothalamus and their likely roles in network dynamics related to energy balance and food intake. This study uses genetic and pharmacological methods to examine the role of CCK-expressing neurons in the VMH (CCKVMH). Namely, using a previously generated BAC transgenic line expressing Cre recombinase under the CCK promoter, we performed targeted manipulations of CCKVMH neurons. Histological and transcriptomic database analysis revealed extensive distribution of these neurons in the VMH, with significant heterogeneity in gene expression related to energy balance, including co-expression with PACAP and somatostatin. Pharmacogenetic acute inhibition via Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) resulted in increased food intake and altered meal patterns, characterized by higher meal frequency and shorter intermeal intervals. Furthermore, diphtheria toxin-mediated ablation of CCKVMH neurons led to significant weight gain and hyperphagia over time, increasing meal size and duration. These mice also exhibited impaired glucose tolerance, indicative of disrupted glucose homeostasis. Our findings underscore the integral role of CCKVMH neurons in modulating feeding behavior, energy homeostasis, and glucose regulation. This study enhances our understanding of the neurohormonal mechanisms underlying obesity and metabolic disorders, providing potential targets for therapeutic interventions.

下丘脑腹内侧核表达胆囊收缩素的神经元控制着能量平衡。
下丘脑是大脑调节能量平衡的主要中枢。腹内侧下丘脑(VMH)通过调节食物摄入、能量消耗和葡萄糖水平,在维持能量平衡方面发挥着核心作用。然而,人们对其功能的细胞和分子机制仍然知之甚少。胆囊收缩素(CCK)是该下丘脑核表达的众多基因之一。外周 CCK 可调节食物摄入量、体重和葡萄糖稳态。然而,目前的研究并未解释 CCK 神经元在下丘脑特定核团中的功能,以及它们在与能量平衡和食物摄入相关的网络动态中可能发挥的作用。本研究利用遗传学和药理学方法研究了VMH(CCKVMH)中表达CCK的神经元的作用。也就是说,利用之前生成的在CCK启动子下表达Cre重组酶的BAC转基因系,我们对CCKVMH神经元进行了靶向操作。组织学和转录组数据库分析表明,这些神经元广泛分布在 VMH 中,与能量平衡相关的基因表达具有显著的异质性,包括与 PACAP 和体生长抑素的共表达。通过设计药物独家激活的设计受体(DREADDs)进行药物遗传学急性抑制,可增加食物摄入量并改变进餐模式,其特点是进餐频率更高,进餐间隔更短。此外,白喉毒素介导的 CCKVMH 神经元消融会导致体重显著增加,并随着时间的推移出现食欲亢进,进餐量增加,进餐时间延长。这些小鼠还表现出葡萄糖耐量受损,表明葡萄糖稳态遭到破坏。我们的发现强调了 CCKVMH 神经元在调节摄食行为、能量平衡和葡萄糖调节中不可或缺的作用。这项研究加深了我们对肥胖和代谢紊乱的神经激素机制的了解,为治疗干预提供了潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
3.80%
发文量
627
审稿时长
6-12 weeks
期刊介绍: Frontiers in Cellular Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the cellular mechanisms underlying cell function in the nervous system across all species. Specialty Chief Editors Egidio D‘Angelo at the University of Pavia and Christian Hansel at the University of Chicago are supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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