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Barakol extracted from cassia siamea stimulates chloride secretion in rat colon

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dc.contributor.author Deachapunya C.
dc.contributor.author Poonyachoti S.
dc.contributor.author Thongsaard W.
dc.contributor.author Krishnamra N.
dc.date.accessioned 2021-04-05T04:32:33Z
dc.date.available 2021-04-05T04:32:33Z
dc.date.issued 2005
dc.identifier.issn 223565
dc.identifier.other 2-s2.0-22944487650
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/15084
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-22944487650&doi=10.1124%2fjpet.105.084210&partnerID=40&md5=ee7670712d1ae43839848193861ac34e
dc.description.abstract Barakol 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.subject amiloride
dc.subject atropine
dc.subject barakol
dc.subject bumetanide
dc.subject chloride
dc.subject efenamic acid
dc.subject glibenclamide
dc.subject hexamethonium
dc.subject indometacin
dc.subject plant extract
dc.subject prostaglandin synthase
dc.subject Ringer solution
dc.subject tetrodotoxin
dc.subject unclassified drug
dc.subject animal tissue
dc.subject anion transport
dc.subject article
dc.subject ascending colon
dc.subject chloride transport
dc.subject colon mucosa
dc.subject concentration response
dc.subject descending colon
dc.subject Eassia simea
dc.subject intestine secretion
dc.subject male
dc.subject nonhuman
dc.subject priority journal
dc.subject rat
dc.subject Senna
dc.subject short circuit current
dc.subject Animals
dc.subject Anti-Anxiety Agents
dc.subject Benzopyrans
dc.subject Bicarbonates
dc.subject Calcium Channel Blockers
dc.subject Cassia
dc.subject Chlorides
dc.subject Colon
dc.subject Cyclooxygenase Inhibitors
dc.subject Electrophysiology
dc.subject Indomethacin
dc.subject Intestinal Mucosa
dc.subject Male
dc.subject Phenalenes
dc.subject Rats
dc.subject Rats, Wistar
dc.subject Sodium-Potassium-Chloride Symporters
dc.subject Stimulation, Chemical
dc.title Barakol extracted from cassia siamea stimulates chloride secretion in rat colon
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Journal of Pharmacology and Experimental Therapeutics. Vol 314, No.2 (2005), p.732-737
dc.identifier.doi 10.1124/jpet.105.084210


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