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Quantitative analysis of TRP channel genes in mouse organs

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dc.contributor.authorJang, Yongwoo-
dc.contributor.authorLee, Yunjong-
dc.contributor.authorKim, Sung Min-
dc.contributor.authorYang, Young Duk-
dc.contributor.authorJung, Jooyoung-
dc.contributor.authorOh, Uhtaek-
dc.date.accessioned2022-07-16T13:28:52Z-
dc.date.available2022-07-16T13:28:52Z-
dc.date.created2021-05-12-
dc.date.issued2012-10-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/164548-
dc.description.abstractThe transient receptor potential (TRP) channel superfamily is a set of channel genes that mediate numerous physiological functions such as sensing irritants or detecting temperature changes. Despite their functions, expressional information on TRP channels in various organs is largely elusive. Therefore, we conducted a systematic quantitative comparison of each mRNA expression level of 22 mouse TRP channels in various organs. As a result, we found that average levels of TRP channel transcripts were very low reaching similar to 3% of the GAPDH transcript level. Among 22 TRP channels, TRPC1 and TRPM7 were most abundant in the majority of organs. In contrast, TRPV3, TRPV5, TRPV6, TRPC7, TRPM1, and TRPM5 elicited very low message profiles throughout the major organs. Consistent with their functions as molecular sensors for irritants and temperature changes, TRPV1, TRPM8 and TRPA1 showed exclusive expression in sensory ganglia. TRPC3 and TRPM3 were abundant in the sensory ganglia and brain. High levels of transcripts of TRPV2, TRPC6, TRPM4, and TRPM6 were observed in the lung. In addition, channel transcript levels were very low except TRPM7 in the liver. In summary, the expression profile of TRP channels in major tissues provides insight to their physiological functions and therefore application to new drug development.-
dc.language영어-
dc.language.isoen-
dc.publisherPHARMACEUTICAL SOC KOREA-
dc.titleQuantitative analysis of TRP channel genes in mouse organs-
dc.typeArticle-
dc.contributor.affiliatedAuthorJang, Yongwoo-
dc.contributor.affiliatedAuthorKim, Sung Min-
dc.identifier.doi10.1007/s12272-012-1016-8-
dc.identifier.scopusid2-s2.0-84872121788-
dc.identifier.wosid000310950500017-
dc.identifier.bibliographicCitationArchives of Pharmacal Research, v.35, no.10, pp.1823 - 1830-
dc.relation.isPartOfArchives of Pharmacal Research-
dc.citation.titleArchives of Pharmacal Research-
dc.citation.volume35-
dc.citation.number10-
dc.citation.startPage1823-
dc.citation.endPage1830-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001707257-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusRECEPTOR POTENTIAL CHANNELS-
dc.subject.keywordPlusCATION CHANNEL-
dc.subject.keywordPlusION-CHANNEL-
dc.subject.keywordPlusTRANSIENT RECEPTOR-
dc.subject.keywordPlusVANILLOID RECEPTOR-
dc.subject.keywordPlusCAPSAICIN-RECEPTOR-
dc.subject.keywordPlusNOXIOUS HEAT-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCOLD-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordAuthorTRPV-
dc.subject.keywordAuthorTRPC-
dc.subject.keywordAuthorTRPM-
dc.subject.keywordAuthorTRPA1-
dc.subject.keywordAuthorTRP channels-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs12272-012-1016-8-
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서울 예술·체육대학 > 서울 체육학과 > 1. Journal Articles
서울 의과대학 > 서울 약리학교실 > 1. Journal Articles

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