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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5140073</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_1744806916681567</sage_id><sourcerecordid>1845823133</sourcerecordid><originalsourceid>FETCH-LOGICAL-c345t-c0c82019c7adb93d6e17357ccffd44bc3d98410a56c17ad045fcd485b453cbba3</originalsourceid><addsrcrecordid>eNp1kTtPwzAUhS0E4lHYmVBGloBd23GyICHEoxISC8yW49y0Lk5c7KTQf4-jlqogMfn63O8ePw5C5wRfESLENRGM5TgrSJblhGdiDx0PUjpo-zv1EToJYY4xFTgjh-hoLApcED4-RnLSLp1dQgNtl7g6aSA4a5rS6KRyC9WYFvw0blroPp1_T0wby97HVjeL8kJFwYM1UCflKuk8qKox1ibwBV6bAKfooFY2wNlmHaG3h_vXu6f0-eVxcnf7nGrKeJdqrPMxJoUWqioLWmVABOVC67quGCs1rYqcEax4pklEMOO1rljOS8apLktFR-hm7bvoywYqHZ_jlZULbxrlV9IpI393WjOTU7eUnDCMBY0GlxsD7z56CJ1sTNBgrWrB9UGSnPF8TAkdULxGtXcheKi3xxAsh1zk31ziyMXu9bYDP0FEIF0DQU1Bzl3v2_hd_xt-A5PfmLM</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1845823133</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>SAGE Journals</source><source>Free Full-Text Journals in Chemistry</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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 & 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.
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><subject>Animals</subject><subject>Clozapine - analogs & derivatives</subject><subject>Clozapine - pharmacology</subject><subject>Disease Models, Animal</subject><subject>Dopamine - metabolism</subject><subject>Dopamine Plasma Membrane Transport Proteins - genetics</subject><subject>Dopamine Plasma Membrane Transport Proteins - metabolism</subject><subject>Exercise Test</subject><subject>Exercise Therapy - methods</subject><subject>Hyperalgesia - etiology</subject><subject>Hyperalgesia - rehabilitation</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Neuralgia - pathology</subject><subject>Neuralgia - rehabilitation</subject><subject>Nucleus Accumbens - drug effects</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Pain Measurement</subject><subject>Pain Threshold - physiology</subject><subject>Phosphopyruvate Hydratase - genetics</subject><subject>Phosphopyruvate Hydratase - metabolism</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Serotonin Antagonists - pharmacology</subject><subject>Tyrosine 3-Monooxygenase - genetics</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><subject>Ventral Tegmental Area - physiopathology</subject><issn>1744-8069</issn><issn>1744-8069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>EIF</sourceid><recordid>eNp1kTtPwzAUhS0E4lHYmVBGloBd23GyICHEoxISC8yW49y0Lk5c7KTQf4-jlqogMfn63O8ePw5C5wRfESLENRGM5TgrSJblhGdiDx0PUjpo-zv1EToJYY4xFTgjh-hoLApcED4-RnLSLp1dQgNtl7g6aSA4a5rS6KRyC9WYFvw0blroPp1_T0wby97HVjeL8kJFwYM1UCflKuk8qKox1ibwBV6bAKfooFY2wNlmHaG3h_vXu6f0-eVxcnf7nGrKeJdqrPMxJoUWqioLWmVABOVC67quGCs1rYqcEax4pklEMOO1rljOS8apLktFR-hm7bvoywYqHZ_jlZULbxrlV9IpI393WjOTU7eUnDCMBY0GlxsD7z56CJ1sTNBgrWrB9UGSnPF8TAkdULxGtXcheKi3xxAsh1zk31ziyMXu9bYDP0FEIF0DQU1Bzl3v2_hd_xt-A5PfmLM</recordid><startdate>20161101</startdate><enddate>20161101</enddate><creator>Wakaizumi, Kenta</creator><creator>Kondo, Takashige</creator><creator>Hamada, Yusuke</creator><creator>Narita, Michiko</creator><creator>Kawabe, Rui</creator><creator>Narita, Hiroki</creator><creator>Watanabe, Moe</creator><creator>Kato, Shigeki</creator><creator>Senba, Emiko</creator><creator>Kobayashi, Kazuto</creator><creator>Kuzumaki, Naoko</creator><creator>Yamanaka, Akihiro</creator><creator>Morisaki, Hiroshi</creator><creator>Narita, Minoru</creator><general>SAGE Publications</general><scope>AFRWT</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161101</creationdate><title>Involvement of mesolimbic dopaminergic network in neuropathic pain relief by treadmill exercise</title><author>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</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 & 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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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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