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Cited 13 time in webofscience Cited 13 time in scopus
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Effects of analgesics and antidepressants on TREK-2 and TRESK currents

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dc.contributor.authorPark, Hyun-
dc.contributor.authorKim, Eun-Jin-
dc.contributor.authorHan, Jaehee-
dc.contributor.authorHan, Jongwoo-
dc.contributor.authorKang, Dawon-
dc.date.accessioned2022-12-26T20:05:29Z-
dc.date.available2022-12-26T20:05:29Z-
dc.date.issued2016-07-
dc.identifier.issn1226-4512-
dc.identifier.issn2093-3827-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/15407-
dc.description.abstractTWIK-related K+ channel-2 (TREK-2) and TWIK-related spinal cord K+ (TRESK) channel are members of two-pore domain K+ channel family. They are well expressed and help to set the resting membrane potential in sensory neurons. Modulation of TREK-2 and TRESK channels are involved in the pathogenesis of pain, and specific activators of TREK-2 and TRESK may be beneficial for the treatment of pain symptoms. However, the effect of commonly used analgesics on TREK-2 and TRESK channels are not known. Here, we investigated the effect of analgesics on TREK-2 and TRESK channels. The effects of analgesics were examined in HEK cells transfected with TREK-2 or TRESK. Amitriptyline, citalopram, escitalopram, and fluoxetine significantly inhibited TREK-2 and TRESK currents in HEK cells (p<0.05, n=10). Acetaminophen, ibuprofen, nabumetone, and bupropion inhibited TRESK, but had no effect on TREK-2. These results show that all analgesics tested in this study inhibit TRESK activity. Further study is needed to identify the mechanisms by which the analgesics modulate TREK-2 and TRESK differently.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.titleEffects of analgesics and antidepressants on TREK-2 and TRESK currents-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4196/kjpp.2016.20.4.379-
dc.identifier.scopusid2-s2.0-84978983193-
dc.identifier.wosid000378860300007-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.20, no.4, pp 379 - 385-
dc.citation.titleKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.citation.volume20-
dc.citation.number4-
dc.citation.startPage379-
dc.citation.endPage385-
dc.type.docTypeArticle-
dc.identifier.kciidART002124892-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.subject.keywordPlusPOTASSIUM CHANNEL-
dc.subject.keywordPlusNEUROPATHIC PAIN-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusFLUOXETINE-
dc.subject.keywordPlusDEPRESSION-
dc.subject.keywordPlusMIGRAINE-
dc.subject.keywordPlusAMITRIPTYLINE-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusBUPROPION-
dc.subject.keywordAuthorAnalgesics-
dc.subject.keywordAuthorBackground potassium channels-
dc.subject.keywordAuthorPain-
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