Literature DB >> 32492498

Lateral hypothalamic area neuropeptides modulate ventral tegmental area dopamine neurons and feeding.

Patricia Perez-Bonilla1, Krystal Santiago-Colon2, Gina M Leinninger3.   

Abstract

Understanding how the brain coordinates energy status with the motivation to eat is crucial to identify strategies to improve disordered body weight. The ventral tegmental area (VTA), known as the core of the mesolimbic system, is of particular interest in this regard because it controls the motivation to consume palatable, calorie-dense foods and to engage in volitional activity. The VTA is largely composed of dopamine (DA) neurons, but modulating these DA neurons has been alternately linked with promoting and suppressing feeding, suggesting heterogeneity in their function. Subsets of VTA DA neurons have recently been described based on their anatomical distribution, electrophysiological features, connectivity and molecular expression, but to date there are no signatures to categorize how DA neurons control feeding. Assessing the neuropeptide receptors expressed by VTA DA neurons may be useful in this regard, as many neuropeptides mediate anorexic or orexigenic responses. In particular, the lateral hypothalamic area (LHA) releases a wide variety of feeding-modulating neuropeptides to the VTA. Since VTA neurons intercept LHA neuropeptides known to either evoke or suppress feeding, expression of the cognate neuropeptide receptors within the VTA may point to VTA DA neuronal mechanisms to promote or suppress feeding, respectively. Here we review the role of the VTA in energy balance and the LHA neuropeptide signaling systems that act in the VTA, whose receptors might be used to classify how VTA DA neurons contribute to energy balance.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Feeding; Lateral hypothalamic area; Melanin-concentrating hormone; Neurotensin; Orexin/hypocretin

Year:  2020        PMID: 32492498      PMCID: PMC7416562          DOI: 10.1016/j.physbeh.2020.112986

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


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