Involvement of mesolimbic dopaminergic network in neuropathic pain relief by treadmill exercise: A study for specific neural control with Gi-DREADD in mice

Background Exercise alleviates pain and it is a central component of treatment strategy for chronic pain in clinical setting. However, little is known about mechanism of this exercise-induced hypoalgesia. The mesolimbic dopaminergic network plays a role in positive emotions to rewards including moti...

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Veröffentlicht in:Molecular pain 2016-11, Vol.12
Hauptverfasser: Wakaizumi, Kenta, Kondo, Takashige, Hamada, Yusuke, Narita, Michiko, Kawabe, Rui, Narita, Hiroki, Watanabe, Moe, Kato, Shigeki, Senba, Emiko, Kobayashi, Kazuto, Kuzumaki, Naoko, Yamanaka, Akihiro, Morisaki, Hiroshi, Narita, Minoru
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container_title Molecular pain
container_volume 12
creator Wakaizumi, Kenta
Kondo, Takashige
Hamada, Yusuke
Narita, Michiko
Kawabe, Rui
Narita, Hiroki
Watanabe, Moe
Kato, Shigeki
Senba, Emiko
Kobayashi, Kazuto
Kuzumaki, Naoko
Yamanaka, Akihiro
Morisaki, Hiroshi
Narita, Minoru
description Background Exercise alleviates pain and it is a central component of treatment strategy for chronic pain in clinical setting. However, little is known about mechanism of this exercise-induced hypoalgesia. The mesolimbic dopaminergic network plays a role in positive emotions to rewards including motivation and pleasure. Pain negatively modulates these emotions, but appropriate exercise is considered to activate the dopaminergic network. We investigated possible involvement of this network as a mechanism of exercise-induced hypoalgesia. Methods In the present study, we developed a protocol of treadmill exercise, which was able to recover pain threshold under partial sciatic nerve ligation in mice, and investigated involvement of the dopaminergic reward network in exercise-induced hypoalgesia. To temporally suppress a neural activation during exercise, a genetically modified inhibitory G-protein-coupled receptor, hM4Di, was specifically expressed on dopaminergic pathway from the ventral tegmental area to the nucleus accumbens. Results The chemogenetic-specific neural suppression by Gi-DREADD system dramatically offset the effect of exercise-induced hypoalgesia in transgenic mice with hM4Di expressed on the ventral tegmental area dopamine neurons. Additionally, anti-exercise-induced hypoalgesia effect was significantly observed under the suppression of neurons projecting out of the ventral tegmental area to the nucleus accumbens as well. Conclusion Our findings suggest that the dopaminergic pathway from the ventral tegmental area to the nucleus accumbens is involved in the anti-nociception under low-intensity exercise under a neuropathic pain-like state.
doi_str_mv 10.1177/1744806916681567
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However, little is known about mechanism of this exercise-induced hypoalgesia. The mesolimbic dopaminergic network plays a role in positive emotions to rewards including motivation and pleasure. Pain negatively modulates these emotions, but appropriate exercise is considered to activate the dopaminergic network. We investigated possible involvement of this network as a mechanism of exercise-induced hypoalgesia. Methods In the present study, we developed a protocol of treadmill exercise, which was able to recover pain threshold under partial sciatic nerve ligation in mice, and investigated involvement of the dopaminergic reward network in exercise-induced hypoalgesia. To temporally suppress a neural activation during exercise, a genetically modified inhibitory G-protein-coupled receptor, hM4Di, was specifically expressed on dopaminergic pathway from the ventral tegmental area to the nucleus accumbens. Results The chemogenetic-specific neural suppression by Gi-DREADD system dramatically offset the effect of exercise-induced hypoalgesia in transgenic mice with hM4Di expressed on the ventral tegmental area dopamine neurons. Additionally, anti-exercise-induced hypoalgesia effect was significantly observed under the suppression of neurons projecting out of the ventral tegmental area to the nucleus accumbens as well. Conclusion Our findings suggest that the dopaminergic pathway from the ventral tegmental area to the nucleus accumbens is involved in the anti-nociception under low-intensity exercise under a neuropathic pain-like state.</description><identifier>ISSN: 1744-8069</identifier><identifier>EISSN: 1744-8069</identifier><identifier>DOI: 10.1177/1744806916681567</identifier><identifier>PMID: 27909152</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Clozapine - analogs &amp; derivatives ; Clozapine - pharmacology ; Disease Models, Animal ; Dopamine - metabolism ; Dopamine Plasma Membrane Transport Proteins - genetics ; Dopamine Plasma Membrane Transport Proteins - metabolism ; Exercise Test ; Exercise Therapy - methods ; Hyperalgesia - etiology ; Hyperalgesia - rehabilitation ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Neuralgia - pathology ; Neuralgia - rehabilitation ; Nucleus Accumbens - drug effects ; Nucleus Accumbens - metabolism ; Pain Measurement ; Pain Threshold - physiology ; Phosphopyruvate Hydratase - genetics ; Phosphopyruvate Hydratase - metabolism ; Receptors, G-Protein-Coupled - metabolism ; Serotonin Antagonists - pharmacology ; Tyrosine 3-Monooxygenase - genetics ; Tyrosine 3-Monooxygenase - metabolism ; Ventral Tegmental Area - physiopathology</subject><ispartof>Molecular pain, 2016-11, Vol.12</ispartof><rights>The Author(s) 2016</rights><rights>The Author(s) 2016.</rights><rights>The Author(s) 2016 2016 SAGE Publications Inc., unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c345t-c0c82019c7adb93d6e17357ccffd44bc3d98410a56c17ad045fcd485b453cbba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140073/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140073/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,21966,27853,27924,27925,44945,45333,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27909152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wakaizumi, Kenta</creatorcontrib><creatorcontrib>Kondo, Takashige</creatorcontrib><creatorcontrib>Hamada, Yusuke</creatorcontrib><creatorcontrib>Narita, Michiko</creatorcontrib><creatorcontrib>Kawabe, Rui</creatorcontrib><creatorcontrib>Narita, Hiroki</creatorcontrib><creatorcontrib>Watanabe, Moe</creatorcontrib><creatorcontrib>Kato, Shigeki</creatorcontrib><creatorcontrib>Senba, Emiko</creatorcontrib><creatorcontrib>Kobayashi, Kazuto</creatorcontrib><creatorcontrib>Kuzumaki, Naoko</creatorcontrib><creatorcontrib>Yamanaka, Akihiro</creatorcontrib><creatorcontrib>Morisaki, Hiroshi</creatorcontrib><creatorcontrib>Narita, Minoru</creatorcontrib><title>Involvement of mesolimbic dopaminergic network in neuropathic pain relief by treadmill exercise: A study for specific neural control with Gi-DREADD in mice</title><title>Molecular pain</title><addtitle>Mol Pain</addtitle><description>Background Exercise alleviates pain and it is a central component of treatment strategy for chronic pain in clinical setting. However, little is known about mechanism of this exercise-induced hypoalgesia. The mesolimbic dopaminergic network plays a role in positive emotions to rewards including motivation and pleasure. Pain negatively modulates these emotions, but appropriate exercise is considered to activate the dopaminergic network. We investigated possible involvement of this network as a mechanism of exercise-induced hypoalgesia. Methods In the present study, we developed a protocol of treadmill exercise, which was able to recover pain threshold under partial sciatic nerve ligation in mice, and investigated involvement of the dopaminergic reward network in exercise-induced hypoalgesia. To temporally suppress a neural activation during exercise, a genetically modified inhibitory G-protein-coupled receptor, hM4Di, was specifically expressed on dopaminergic pathway from the ventral tegmental area to the nucleus accumbens. Results The chemogenetic-specific neural suppression by Gi-DREADD system dramatically offset the effect of exercise-induced hypoalgesia in transgenic mice with hM4Di expressed on the ventral tegmental area dopamine neurons. Additionally, anti-exercise-induced hypoalgesia effect was significantly observed under the suppression of neurons projecting out of the ventral tegmental area to the nucleus accumbens as well. 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Kondo, Takashige ; Hamada, Yusuke ; Narita, Michiko ; Kawabe, Rui ; Narita, Hiroki ; Watanabe, Moe ; Kato, Shigeki ; Senba, Emiko ; Kobayashi, Kazuto ; Kuzumaki, Naoko ; Yamanaka, Akihiro ; Morisaki, Hiroshi ; Narita, Minoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-c0c82019c7adb93d6e17357ccffd44bc3d98410a56c17ad045fcd485b453cbba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Clozapine - analogs &amp; derivatives</topic><topic>Clozapine - pharmacology</topic><topic>Disease Models, Animal</topic><topic>Dopamine - metabolism</topic><topic>Dopamine Plasma Membrane Transport Proteins - genetics</topic><topic>Dopamine Plasma Membrane Transport Proteins - metabolism</topic><topic>Exercise Test</topic><topic>Exercise Therapy - methods</topic><topic>Hyperalgesia - etiology</topic><topic>Hyperalgesia - rehabilitation</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Neuralgia - pathology</topic><topic>Neuralgia - rehabilitation</topic><topic>Nucleus Accumbens - drug effects</topic><topic>Nucleus Accumbens - metabolism</topic><topic>Pain Measurement</topic><topic>Pain Threshold - physiology</topic><topic>Phosphopyruvate Hydratase - genetics</topic><topic>Phosphopyruvate Hydratase - metabolism</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Serotonin Antagonists - pharmacology</topic><topic>Tyrosine 3-Monooxygenase - genetics</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><topic>Ventral Tegmental Area - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wakaizumi, Kenta</creatorcontrib><creatorcontrib>Kondo, Takashige</creatorcontrib><creatorcontrib>Hamada, Yusuke</creatorcontrib><creatorcontrib>Narita, Michiko</creatorcontrib><creatorcontrib>Kawabe, Rui</creatorcontrib><creatorcontrib>Narita, Hiroki</creatorcontrib><creatorcontrib>Watanabe, Moe</creatorcontrib><creatorcontrib>Kato, Shigeki</creatorcontrib><creatorcontrib>Senba, Emiko</creatorcontrib><creatorcontrib>Kobayashi, Kazuto</creatorcontrib><creatorcontrib>Kuzumaki, Naoko</creatorcontrib><creatorcontrib>Yamanaka, Akihiro</creatorcontrib><creatorcontrib>Morisaki, Hiroshi</creatorcontrib><creatorcontrib>Narita, Minoru</creatorcontrib><collection>SAGE Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular pain</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wakaizumi, Kenta</au><au>Kondo, Takashige</au><au>Hamada, Yusuke</au><au>Narita, Michiko</au><au>Kawabe, Rui</au><au>Narita, Hiroki</au><au>Watanabe, Moe</au><au>Kato, Shigeki</au><au>Senba, Emiko</au><au>Kobayashi, Kazuto</au><au>Kuzumaki, Naoko</au><au>Yamanaka, Akihiro</au><au>Morisaki, Hiroshi</au><au>Narita, Minoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Involvement of mesolimbic dopaminergic network in neuropathic pain relief by treadmill exercise: A study for specific neural control with Gi-DREADD in mice</atitle><jtitle>Molecular pain</jtitle><addtitle>Mol Pain</addtitle><date>2016-11-01</date><risdate>2016</risdate><volume>12</volume><issn>1744-8069</issn><eissn>1744-8069</eissn><abstract>Background Exercise alleviates pain and it is a central component of treatment strategy for chronic pain in clinical setting. However, little is known about mechanism of this exercise-induced hypoalgesia. The mesolimbic dopaminergic network plays a role in positive emotions to rewards including motivation and pleasure. Pain negatively modulates these emotions, but appropriate exercise is considered to activate the dopaminergic network. We investigated possible involvement of this network as a mechanism of exercise-induced hypoalgesia. Methods In the present study, we developed a protocol of treadmill exercise, which was able to recover pain threshold under partial sciatic nerve ligation in mice, and investigated involvement of the dopaminergic reward network in exercise-induced hypoalgesia. To temporally suppress a neural activation during exercise, a genetically modified inhibitory G-protein-coupled receptor, hM4Di, was specifically expressed on dopaminergic pathway from the ventral tegmental area to the nucleus accumbens. Results The chemogenetic-specific neural suppression by Gi-DREADD system dramatically offset the effect of exercise-induced hypoalgesia in transgenic mice with hM4Di expressed on the ventral tegmental area dopamine neurons. Additionally, anti-exercise-induced hypoalgesia effect was significantly observed under the suppression of neurons projecting out of the ventral tegmental area to the nucleus accumbens as well. Conclusion Our findings suggest that the dopaminergic pathway from the ventral tegmental area to the nucleus accumbens is involved in the anti-nociception under low-intensity exercise under a neuropathic pain-like state.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>27909152</pmid><doi>10.1177/1744806916681567</doi><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; SAGE Journals; Free Full-Text Journals in Chemistry
subjects Animals
Clozapine - analogs & derivatives
Clozapine - pharmacology
Disease Models, Animal
Dopamine - metabolism
Dopamine Plasma Membrane Transport Proteins - genetics
Dopamine Plasma Membrane Transport Proteins - metabolism
Exercise Test
Exercise Therapy - methods
Hyperalgesia - etiology
Hyperalgesia - rehabilitation
Mice
Mice, Inbred C57BL
Mice, Transgenic
Neuralgia - pathology
Neuralgia - rehabilitation
Nucleus Accumbens - drug effects
Nucleus Accumbens - metabolism
Pain Measurement
Pain Threshold - physiology
Phosphopyruvate Hydratase - genetics
Phosphopyruvate Hydratase - metabolism
Receptors, G-Protein-Coupled - metabolism
Serotonin Antagonists - pharmacology
Tyrosine 3-Monooxygenase - genetics
Tyrosine 3-Monooxygenase - metabolism
Ventral Tegmental Area - physiopathology
title Involvement of mesolimbic dopaminergic network in neuropathic pain relief by treadmill exercise: A study for specific neural control with Gi-DREADD in mice
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