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Title: | Barakol extracted from cassia siamea stimulates chloride secretion in rat colon |
Authors: | Deachapunya C. Poonyachoti S. Thongsaard W. Krishnamra N. |
Keywords: | amiloride atropine barakol bumetanide chloride efenamic acid glibenclamide hexamethonium indometacin plant extract prostaglandin synthase Ringer solution tetrodotoxin unclassified drug animal tissue anion transport article ascending colon chloride transport colon mucosa concentration response descending colon Eassia simea intestine secretion male nonhuman priority journal rat Senna short circuit current Animals Anti-Anxiety Agents Benzopyrans Bicarbonates Calcium Channel Blockers Cassia Chlorides Colon Cyclooxygenase Inhibitors Electrophysiology Indomethacin Intestinal Mucosa Male Phenalenes Rats Rats, Wistar Sodium-Potassium-Chloride Symporters Stimulation, Chemical |
Issue Date: | 2005 |
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. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/15084 https://www.scopus.com/inward/record.uri?eid=2-s2.0-22944487650&doi=10.1124%2fjpet.105.084210&partnerID=40&md5=ee7670712d1ae43839848193861ac34e |
ISSN: | 223565 |
Appears in Collections: | Scopus 1983-2021 |
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