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Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice

Self-grooming plays an essential role in hygiene maintenance, thermoregulation, and stress response. However, the neural populations involved in self-grooming remain largely unknown. The paraventricular hypothalamic nucleus (PVH) has been implicated in the regulation of self-grooming. Arginine vasop...

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Autores principales: Islam, Md Tarikul, Maejima, Takashi, Matsui, Ayako, Mieda, Michihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125887/
https://www.ncbi.nlm.nih.gov/pubmed/35606816
http://dx.doi.org/10.1186/s13041-022-00932-9
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author Islam, Md Tarikul
Maejima, Takashi
Matsui, Ayako
Mieda, Michihiro
author_facet Islam, Md Tarikul
Maejima, Takashi
Matsui, Ayako
Mieda, Michihiro
author_sort Islam, Md Tarikul
collection PubMed
description Self-grooming plays an essential role in hygiene maintenance, thermoregulation, and stress response. However, the neural populations involved in self-grooming remain largely unknown. The paraventricular hypothalamic nucleus (PVH) has been implicated in the regulation of self-grooming. Arginine vasopressin-producing neurons are among the major neuronal populations in the PVH (PVH(AVP)), which play important roles in water homeostasis, blood pressure regulation, feeding, and stress response. Here, we report the critical role of PVH(AVP) neurons in the induction of self-grooming. Optogenetic activation of PVH(AVP) neurons immediately induced self-grooming in freely moving mice. Chemogenetic activation of these neurons also increased time spent self-grooming. In contrast, their chemogenetic inhibition significantly reduced naturally occurring self-grooming, suggesting that PVH(AVP)-induced grooming has physiological relevance. Notably, optogenetic activation of PVH(AVP) neurons triggered self-grooming over other adaptive behaviors, such as voracious feeding induced by fasting and social interaction with female mice. Thus, our study proposes the novel role of PVH(AVP) neurons in regulating self-grooming behavior and, consequently, hygiene maintenance and stress response. Furthermore, uncontrolled activation of these neurons may be potentially relevant to diseases characterized by compulsive behaviors and impaired social interaction, such as autism, obsessive–compulsive disorder, and anorexia nervosa. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-022-00932-9.
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spelling pubmed-91258872022-05-24 Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice Islam, Md Tarikul Maejima, Takashi Matsui, Ayako Mieda, Michihiro Mol Brain Research Self-grooming plays an essential role in hygiene maintenance, thermoregulation, and stress response. However, the neural populations involved in self-grooming remain largely unknown. The paraventricular hypothalamic nucleus (PVH) has been implicated in the regulation of self-grooming. Arginine vasopressin-producing neurons are among the major neuronal populations in the PVH (PVH(AVP)), which play important roles in water homeostasis, blood pressure regulation, feeding, and stress response. Here, we report the critical role of PVH(AVP) neurons in the induction of self-grooming. Optogenetic activation of PVH(AVP) neurons immediately induced self-grooming in freely moving mice. Chemogenetic activation of these neurons also increased time spent self-grooming. In contrast, their chemogenetic inhibition significantly reduced naturally occurring self-grooming, suggesting that PVH(AVP)-induced grooming has physiological relevance. Notably, optogenetic activation of PVH(AVP) neurons triggered self-grooming over other adaptive behaviors, such as voracious feeding induced by fasting and social interaction with female mice. Thus, our study proposes the novel role of PVH(AVP) neurons in regulating self-grooming behavior and, consequently, hygiene maintenance and stress response. Furthermore, uncontrolled activation of these neurons may be potentially relevant to diseases characterized by compulsive behaviors and impaired social interaction, such as autism, obsessive–compulsive disorder, and anorexia nervosa. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-022-00932-9. BioMed Central 2022-05-23 /pmc/articles/PMC9125887/ /pubmed/35606816 http://dx.doi.org/10.1186/s13041-022-00932-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Islam, Md Tarikul
Maejima, Takashi
Matsui, Ayako
Mieda, Michihiro
Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
title Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
title_full Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
title_fullStr Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
title_full_unstemmed Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
title_short Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
title_sort paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125887/
https://www.ncbi.nlm.nih.gov/pubmed/35606816
http://dx.doi.org/10.1186/s13041-022-00932-9
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