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dc.contributor.author서은경*
dc.date.accessioned2016-08-29T11:08:48Z-
dc.date.available2016-08-29T11:08:48Z-
dc.date.issued2009*
dc.identifier.issn0014-2999*
dc.identifier.otherOAK-5775*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/232002-
dc.description.abstractPoria cocos Wolf (P. cocos Wolf) is used to treat chronic gastritis, edema, nephrosis, gastric atony, acute gastroenteric catarrh, dizziness, emesis and vomiting. Triterpenoids are a class of natural compounds produced by P. cocos Wolf that contain acyclic 30-carbon precursors. In this study, we investigated the effect of triterpenoids (PA, Pachymic acid; DA, dehydroeburicoic acid; HA, 3β-hydroxylanosta-7,9(11),24-trien-21-oic acid) on human 5-hydroxytryptamine 3A (5-HT 3A) receptor channel activity, which is one of the ligand-gated ion channel families. The two-electrode voltage-clamp technique was used to examine the 5-HT3A mediated current. The inhibitory effect of triterpenoids on 5HT-induced inward current (I 5-HT) occurred in a concentration dependent and reversible manner. Furthermore, the half-inhibitory concentrations (IC 50) of PA, DA and HA were 3.2 ± 0.2, 5.5 ± 0.6 and 1.4 ± 0.2 μM, respectively. This corresponded to an order of potency for the inhibition of I 5-HT in oocytes expressing human 5-HT 3A receptor of HA > PA > DA. Finally, inhibition of I 5HT by triterpenoids occurred in a non-competitive manner, while inhibition by HA and PA showed more voltage-dependency. Taken together, these results indicate that triterpenoids may regulate the expressed 5-HT 3A receptors in Xenopus oocytes. Furthermore, this regulation of the ligand-gated ion channel activity by triterpenoids may be one of the pharmacological actions of P. cocos Wolf. © 2009 Elsevier B.V. All rights reserved.*
dc.languageEnglish*
dc.titleEffects of triterpenoids from Poria cocos Wolf on the serotonin type 3A receptor-mediated ion current in Xenopus oocytes*
dc.typeArticle*
dc.relation.issue41277*
dc.relation.volume615*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage27*
dc.relation.lastpage32*
dc.relation.journaltitleEuropean Journal of Pharmacology*
dc.identifier.doi10.1016/j.ejphar.2009.04.063*
dc.identifier.wosidWOS:000268218100004*
dc.identifier.scopusid2-s2.0-67449152244*
dc.author.googleLee J.-H.*
dc.author.googleLee Y.J.*
dc.author.googleShin J.-K.*
dc.author.googleNam J.-W.*
dc.author.googleNah S.-Y.*
dc.author.googleKim S.-H.*
dc.author.googleJeong J.-H.*
dc.author.googleKim Y.*
dc.author.googleShin M.*
dc.author.googleHong M.*
dc.author.googleSeo E.-K.*
dc.author.googleBae H.*
dc.contributor.scopusid서은경(7005953758)*
dc.date.modifydate20240118144717*
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약학대학 > 약학과 > Journal papers
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