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Cited 14 time in webofscience Cited 18 time in scopus
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The GABA(B) receptor associates with regulators of G-protein signaling 4 protein in the mouse prefrontal cortex and hypothalamus

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dc.contributor.authorKim, Gyeongwha-
dc.contributor.authorJung, Soonwoong-
dc.contributor.authorSon, Hyeonwi-
dc.contributor.authorKim, Sujeong-
dc.contributor.authorChoi, Jungil-
dc.contributor.authorLee, Dong Hoon-
dc.contributor.authorRoh, Gu Seob-
dc.contributor.authorKang, Sang Soo-
dc.contributor.authorCho, Gyeong Jae-
dc.contributor.authorChoi, Wan Sung-
dc.contributor.authorKim, Hyun Joon-
dc.date.accessioned2022-12-26T23:05:03Z-
dc.date.available2022-12-26T23:05:03Z-
dc.date.issued2014-06-
dc.identifier.issn1976-6696-
dc.identifier.issn1976-670X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/18940-
dc.description.abstractRegulators of G-protein signaling (RGS) proteins regulate certain G-protein-coupled receptor (GPCR)-mediated signaling pathways. The GABA(B) receptor (GABA(B)R) is a GPCR that plays a role in the stress response. Previous studies indicate that acute immobilization stress (AIS) decreases RGS4 in the prefrontal cortex (PFC) and hypothalamus (HY) and suggest the possibility of a signal complex composed of RGS4 and GABA(B)R. Therefore, in the present study, we tested whether RGS4 associates with GABA(B)R in these brain regions. We found the co-localization of RGS4 and GABA(B)R subtypes in the PFC and HY using double immunohistochemistry and confirmed a direct association between GABA(B2)R and RGS4 proteins using co-immunoprecipitation. Furthermore, we found that AIS decreased the amount of RGS4 bound to GABA(B2)R and the number of double-positive cells. These results indicate that GABA(B)R forms a signal complex with RGS4 and suggests that RGS4 is a regulator of GABA(B)R.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisher생화학분자생물학회-
dc.titleThe GABA(B) receptor associates with regulators of G-protein signaling 4 protein in the mouse prefrontal cortex and hypothalamus-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.5483/BMBRep.2014.47.6.162-
dc.identifier.scopusid2-s2.0-84903582081-
dc.identifier.wosid000338696400004-
dc.identifier.bibliographicCitationBMB Reports, v.47, no.6, pp 324 - 329-
dc.citation.titleBMB Reports-
dc.citation.volume47-
dc.citation.number6-
dc.citation.startPage324-
dc.citation.endPage329-
dc.type.docTypeArticle-
dc.identifier.kciidART001883451-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusPARAVENTRICULAR NUCLEUS-
dc.subject.keywordPlusGIRK CHANNELS-
dc.subject.keywordPlusRGS PROTEINS-
dc.subject.keywordPlusSTRESS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusMODULATION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusSUBUNITS-
dc.subject.keywordPlusLIGANDS-
dc.subject.keywordAuthorGABA(B) receptor-
dc.subject.keywordAuthorHypothalamus-
dc.subject.keywordAuthorPrefrontal cortex-
dc.subject.keywordAuthorRGS4-
dc.subject.keywordAuthorStress response-
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