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Membrane-Delimited Coupling of TRPV1 and mGluR5 on Presynaptic Terminals of Nociceptive Neurons

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dc.contributor.authorKim, Yong Ho-
dc.contributor.authorPark, Chul-Kyu-
dc.contributor.authorBack, Seung Keun-
dc.contributor.authorLee, C. Justin-
dc.contributor.authorHwang, Se Jin-
dc.contributor.authorBae, Yong Chul-
dc.contributor.authorNa, Heung Sik-
dc.contributor.authorKim, Joong Soo-
dc.contributor.authorJung, Sung Jun-
dc.contributor.authorOh, Seog Bae-
dc.date.accessioned2022-12-20T21:29:14Z-
dc.date.available2022-12-20T21:29:14Z-
dc.date.issued2009-08-
dc.identifier.issn0270-6474-
dc.identifier.issn1529-2401-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/176443-
dc.description.abstractTransient receptor potential vanilloid subtype 1 (TRPV1) and metabotropic glutamate receptor 5 (mGluR5) located on peripheral sensory terminals have been shown to play critical roles in the transduction and modulation of pain sensation. To date, however, very little is known regarding the significance of functional expression of mGluR5 and TRPV1 on the central terminals of sensory neurons in the dorsal horn of the spinal cord. Here we show that TRPV1 on central presynaptic terminals is coupled to mGluR5 in a membrane-delimited manner, thereby contributing to the modulation of nociceptive synaptic transmission in the substantia gelatinosa neurons of the spinal cord. Further, our results demonstrate that TRPV1 is involved in the pain behaviors induced by spinal mGluR5 activation, and diacylglycerol produced by the activation of mGluR5 mediates functional coupling of mGluR5 and TRPV1 on the presynaptic terminals. Thus, mGluR5-TRPV1 coupling on the central presynaptic terminals of nociceptive neurons may be an important mechanism underlying central sensitization under pathological pain conditions.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherSociety for Neuroscience-
dc.titleMembrane-Delimited Coupling of TRPV1 and mGluR5 on Presynaptic Terminals of Nociceptive Neurons-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1523/JNEUROSCI.5030-08.2009-
dc.identifier.scopusid2-s2.0-68849094156-
dc.identifier.wosid000268887300008-
dc.identifier.bibliographicCitationJournal of Neuroscience, v.29, no.32, pp 10000 - 10009-
dc.citation.titleJournal of Neuroscience-
dc.citation.volume29-
dc.citation.number32-
dc.citation.startPage10000-
dc.citation.endPage10009-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusMETABOTROPIC GLUTAMATE RECEPTORS-
dc.subject.keywordPlusRAT SPINAL-CORD-
dc.subject.keywordPlusVANILLOID RECEPTOR-
dc.subject.keywordPlusDORSAL-HORN-
dc.subject.keywordPlusCAPSAICIN RECEPTOR-
dc.subject.keywordPlusSYNAPTIC-TRANSMISSION-
dc.subject.keywordPlusSUBSTANTIA-GELATINOSA-
dc.subject.keywordPlusSUPERFICIAL LAMINAE-
dc.subject.keywordPlusPOTENTIAL CHANNELS-
dc.subject.keywordPlusDIRECT ACTIVATION-
dc.identifier.urlhttps://www.jneurosci.org/content/29/32/10000-
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서울 의과대학 > 서울 생리학교실 > 1. Journal Articles
서울 의과대학 > 서울 해부·세포생물학교실 > 1. Journal Articles

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서울 의과대학 (DEPARTMENT OF ANATOMY AND CELL BIOLOGY)
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