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dc.contributor.authorDeachapunya C.
dc.contributor.authorPoonyachoti S.
dc.contributor.authorThongsaard W.
dc.contributor.authorKrishnamra N.
dc.date.accessioned2021-04-05T04:32:33Z-
dc.date.available2021-04-05T04:32:33Z-
dc.date.issued2005
dc.identifier.issn223565
dc.identifier.other2-s2.0-22944487650
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15084-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-22944487650&doi=10.1124%2fjpet.105.084210&partnerID=40&md5=ee7670712d1ae43839848193861ac34e
dc.description.abstractBarakol is a purified extract of Cassia siamea, a plant that has been used as a laxative in traditional medicine. In this study, the effect of barakol on anion transport across the rat colon epithelium was investigated. Colonic epithelium was mounted in Ussing chambers and bathed with Ringer's solution. Addition of 1 mM barakol to the basolateral solution produced a slow increase in short-circuit current (Isc) in proximal colon and distal colon by 24.5 ± 2.2 and 24.2 ± 1.4 μA/cm2, respectively. Barakol increased Isc in a concentration-dependent manner with an EC50 value of 0.4 mM. The barakol-stimulated increase in Isc was inhibited by subsequent treatment with 500 μM diphenylamine-2-carboxylic acid or 400 μM glibenclamide added to the apical solution and 200 μM bumetanide added to the basolateral solution. Pretreatment of the tissues with 200 μM bumetanide, but not 10 μM amiloride, completely abolished the barakol-increased Isc. Ion substitution experiments showed an inhibition of barakol-stimulated Isc in chloride-free solution but not in bicarbonate-free solution. In addition, pretreatment of tissues with 10 μM tetrodotoxin or 10 μM indomethacin, but not 1 μM atropine or 10 μM hexamethonium, partially inhibited the Isc response by barakol. The present results demonstrated the stimulatory effect of barakol on the bumetanide-sensitive chloride secretion in rat colon. The effect of barakol was partly mediated by the stimulation of submucosal nerves and through the release of cyclooxygenase metabolites. These findings thus provide an explanation for the underlying mechanism of barakol as a secretagogue in mammalian colon. Copyright © 2005 by The American Society for Pharmacology and Experimental Therapeutics.
dc.subjectamiloride
dc.subjectatropine
dc.subjectbarakol
dc.subjectbumetanide
dc.subjectchloride
dc.subjectefenamic acid
dc.subjectglibenclamide
dc.subjecthexamethonium
dc.subjectindometacin
dc.subjectplant extract
dc.subjectprostaglandin synthase
dc.subjectRinger solution
dc.subjecttetrodotoxin
dc.subjectunclassified drug
dc.subjectanimal tissue
dc.subjectanion transport
dc.subjectarticle
dc.subjectascending colon
dc.subjectchloride transport
dc.subjectcolon mucosa
dc.subjectconcentration response
dc.subjectdescending colon
dc.subjectEassia simea
dc.subjectintestine secretion
dc.subjectmale
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectrat
dc.subjectSenna
dc.subjectshort circuit current
dc.subjectAnimals
dc.subjectAnti-Anxiety Agents
dc.subjectBenzopyrans
dc.subjectBicarbonates
dc.subjectCalcium Channel Blockers
dc.subjectCassia
dc.subjectChlorides
dc.subjectColon
dc.subjectCyclooxygenase Inhibitors
dc.subjectElectrophysiology
dc.subjectIndomethacin
dc.subjectIntestinal Mucosa
dc.subjectMale
dc.subjectPhenalenes
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectSodium-Potassium-Chloride Symporters
dc.subjectStimulation, Chemical
dc.titleBarakol extracted from cassia siamea stimulates chloride secretion in rat colon
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of Pharmacology and Experimental Therapeutics. Vol 314, No.2 (2005), p.732-737
dc.identifier.doi10.1124/jpet.105.084210
Appears in Collections:Scopus 1983-2021

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