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Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine

INTRODUCTION: The lateral hypothalamus (LH) plays an important physiological role in brain function and also plays an important role in substance abuse. The neuropeptides called orexin (or hypocretins) have been identified as being located exclusively in the cell bodies of the LH. Our previous studi...

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Autores principales: Jang, Han Byeol, Ahn, DanBi, Kim, Hyung Kyu, Guan, Xiaowei, Fan, Yu, Lee, Bae Hwan, Kim, Hee Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369078/
https://www.ncbi.nlm.nih.gov/pubmed/37501724
http://dx.doi.org/10.3389/fnmol.2023.1195939
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author Jang, Han Byeol
Ahn, DanBi
Kim, Hyung Kyu
Guan, Xiaowei
Fan, Yu
Lee, Bae Hwan
Kim, Hee Young
author_facet Jang, Han Byeol
Ahn, DanBi
Kim, Hyung Kyu
Guan, Xiaowei
Fan, Yu
Lee, Bae Hwan
Kim, Hee Young
author_sort Jang, Han Byeol
collection PubMed
description INTRODUCTION: The lateral hypothalamus (LH) plays an important physiological role in brain function and also plays an important role in substance abuse. The neuropeptides called orexin (or hypocretins) have been identified as being located exclusively in the cell bodies of the LH. Our previous studies have demonstrated that mechanical stimulation (MS) of the ulnar nerve produces strong inhibitory effects on cocaine addiction–like behaviors through activation of LH projection to the lateral habenula (LHb). METHODS: Therefore, the present study hypothesized that ulnar MS would suppress the psychomotor responses induced by cocaine through the orexinergic LH-to-LHb pathway. RESULTS: Ulnar MS attenuated cocaine enhancement of locomotor activity and 50-kHz ultrasonic vocalizations, which was prevented by antagonism of orexin-receptor type 2 (OX2R) in the LHb. Injection of orexin-A into the LHb reduced the cocaine-induced psychomotor responses. MS of the ulnar nerve excited LH orexinergic neurons. In addition, the excitation of LHb neurons by MS was blocked by the systemic administration of an OX2R antagonist. DISCUSSION: These findings suggest that MS applied to the ulnar nerve recruits an orexinergic LH-to-LHb pathway to suppress the psychomotor responses induced by cocaine.
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spelling pubmed-103690782023-07-27 Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine Jang, Han Byeol Ahn, DanBi Kim, Hyung Kyu Guan, Xiaowei Fan, Yu Lee, Bae Hwan Kim, Hee Young Front Mol Neurosci Molecular Neuroscience INTRODUCTION: The lateral hypothalamus (LH) plays an important physiological role in brain function and also plays an important role in substance abuse. The neuropeptides called orexin (or hypocretins) have been identified as being located exclusively in the cell bodies of the LH. Our previous studies have demonstrated that mechanical stimulation (MS) of the ulnar nerve produces strong inhibitory effects on cocaine addiction–like behaviors through activation of LH projection to the lateral habenula (LHb). METHODS: Therefore, the present study hypothesized that ulnar MS would suppress the psychomotor responses induced by cocaine through the orexinergic LH-to-LHb pathway. RESULTS: Ulnar MS attenuated cocaine enhancement of locomotor activity and 50-kHz ultrasonic vocalizations, which was prevented by antagonism of orexin-receptor type 2 (OX2R) in the LHb. Injection of orexin-A into the LHb reduced the cocaine-induced psychomotor responses. MS of the ulnar nerve excited LH orexinergic neurons. In addition, the excitation of LHb neurons by MS was blocked by the systemic administration of an OX2R antagonist. DISCUSSION: These findings suggest that MS applied to the ulnar nerve recruits an orexinergic LH-to-LHb pathway to suppress the psychomotor responses induced by cocaine. Frontiers Media S.A. 2023-07-12 /pmc/articles/PMC10369078/ /pubmed/37501724 http://dx.doi.org/10.3389/fnmol.2023.1195939 Text en Copyright © 2023 Jang, Ahn, Kim, Guan, Fan, Lee and Kim. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Neuroscience
Jang, Han Byeol
Ahn, DanBi
Kim, Hyung Kyu
Guan, Xiaowei
Fan, Yu
Lee, Bae Hwan
Kim, Hee Young
Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine
title Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine
title_full Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine
title_fullStr Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine
title_full_unstemmed Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine
title_short Mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine
title_sort mediation of lateral hypothalamus orexin input to lateral habenula in the inhibitory effects of mechanical stimulation on psychomotor responses induced by cocaine
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369078/
https://www.ncbi.nlm.nih.gov/pubmed/37501724
http://dx.doi.org/10.3389/fnmol.2023.1195939
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