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Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1

Adiponectin, a metabolic hormone secreted by adipocytes, can cross the blood–brain barrier to act on neurons in different brain regions, including those involved in stress-related disorders. Here we show that dopamine neurons in the ventral tegmental area (VTA) express adiponectin receptor 1 (AdipoR...

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Autores principales: Sun, Fengjiao, Lei, Yun, You, Jingjing, Li, Chen, Sun, Linshan, Garza, Jacob, Zhang, Di, Guo, Ming, Scherer, Phillip E., Lodge, Daniel, Lu, Xin-Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325675/
https://www.ncbi.nlm.nih.gov/pubmed/29988086
http://dx.doi.org/10.1038/s41380-018-0102-9
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author Sun, Fengjiao
Lei, Yun
You, Jingjing
Li, Chen
Sun, Linshan
Garza, Jacob
Zhang, Di
Guo, Ming
Scherer, Phillip E.
Lodge, Daniel
Lu, Xin-Yun
author_facet Sun, Fengjiao
Lei, Yun
You, Jingjing
Li, Chen
Sun, Linshan
Garza, Jacob
Zhang, Di
Guo, Ming
Scherer, Phillip E.
Lodge, Daniel
Lu, Xin-Yun
author_sort Sun, Fengjiao
collection PubMed
description Adiponectin, a metabolic hormone secreted by adipocytes, can cross the blood–brain barrier to act on neurons in different brain regions, including those involved in stress-related disorders. Here we show that dopamine neurons in the ventral tegmental area (VTA) express adiponectin receptor 1 (AdipoR1). Intra-VTA infusion of adiponectin or the adiponectin mimetic AdipoRon in wild-type mice decreases basal dopamine neuron population activity and firing rate and reverses the restraint stress-induced increase in dopamine neuron activity and anxiety behavior. Adiponectin haploinsufficiency leads to increased dopamine neuron firing and anxiety behavior under basal conditions. Ablation of AdipoR1 specifically from dopamine neurons enhances neuronal and anxiogenic responses to restraint stress. The effects of intra-VTA infusion of adiponectin on neuronal activity and behavior were abolished in mice lacking AdipoR1 in dopamine neurons. These observations indicate that adiponectin can directly modulate VTA dopamine neuron activity and anxiety behavior, and that AdipoR1 is required for adiponectin-induced inhibition of dopamine neurons and anxiolytic effects. These results strengthen the idea of adiponectin as a key biological factor that links metabolic syndrome and emotional disorders.
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spelling pubmed-63256752019-01-11 Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1 Sun, Fengjiao Lei, Yun You, Jingjing Li, Chen Sun, Linshan Garza, Jacob Zhang, Di Guo, Ming Scherer, Phillip E. Lodge, Daniel Lu, Xin-Yun Mol Psychiatry Article Adiponectin, a metabolic hormone secreted by adipocytes, can cross the blood–brain barrier to act on neurons in different brain regions, including those involved in stress-related disorders. Here we show that dopamine neurons in the ventral tegmental area (VTA) express adiponectin receptor 1 (AdipoR1). Intra-VTA infusion of adiponectin or the adiponectin mimetic AdipoRon in wild-type mice decreases basal dopamine neuron population activity and firing rate and reverses the restraint stress-induced increase in dopamine neuron activity and anxiety behavior. Adiponectin haploinsufficiency leads to increased dopamine neuron firing and anxiety behavior under basal conditions. Ablation of AdipoR1 specifically from dopamine neurons enhances neuronal and anxiogenic responses to restraint stress. The effects of intra-VTA infusion of adiponectin on neuronal activity and behavior were abolished in mice lacking AdipoR1 in dopamine neurons. These observations indicate that adiponectin can directly modulate VTA dopamine neuron activity and anxiety behavior, and that AdipoR1 is required for adiponectin-induced inhibition of dopamine neurons and anxiolytic effects. These results strengthen the idea of adiponectin as a key biological factor that links metabolic syndrome and emotional disorders. Nature Publishing Group UK 2018-07-09 2019 /pmc/articles/PMC6325675/ /pubmed/29988086 http://dx.doi.org/10.1038/s41380-018-0102-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sun, Fengjiao
Lei, Yun
You, Jingjing
Li, Chen
Sun, Linshan
Garza, Jacob
Zhang, Di
Guo, Ming
Scherer, Phillip E.
Lodge, Daniel
Lu, Xin-Yun
Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1
title Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1
title_full Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1
title_fullStr Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1
title_full_unstemmed Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1
title_short Adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through AdipoR1
title_sort adiponectin modulates ventral tegmental area dopamine neuron activity and anxiety-related behavior through adipor1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325675/
https://www.ncbi.nlm.nih.gov/pubmed/29988086
http://dx.doi.org/10.1038/s41380-018-0102-9
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