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Am J Physiol Gastrointest Liver Physiol ; 282(3): G508-18, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11842001

ABSTRACT

The effect of baicalein on mucosal ion transport in the rat distal colon was investigated in Ussing chambers. Mucosal addition of baicalein (1-100 microM) elicited a concentration-dependent short-circuit current (I(sc)) response. The increase in I(sc) was mainly due to Cl(-) secretion. The presence of mucosal indomethacin (10 microM) significantly reduced both the basal and subsequent baicalein-evoked I(sc) responses. The baicalein-induced I(sc) were inhibited by mucosal application of diphenylamine-2-carboxylic acid (100 microM) and glibenclamide (500 microM) and basolateral application of chromanol 293B (30 microM), a blocker of K(v)LQT1 channels and Ba(2+) ions (5 mM). Treatment of the colonic mucosa with baicalein elicited a threefold increase in cAMP production. Pretreating the colonic mucosa with carbachol (100 microM, serosal) but not thapsigargin (1 microM, both sides) abolished the baicalein-induced I(sc). Addition of baicalein subsequent to forskolin induced a further increase in I(sc). These results indicate that the baicalein evoked Cl(-) secretion across rat colonic mucosa, possibly via a cAMP-dependent pathway. However, the action of baicalein cannot be solely explained by its cAMP-elevating effect. Baicalein may stimulate Cl(-) secretion via a cAMP-independent pathway or have a direct effect on cystic fibrosis transmembrane conductance regulator.


Subject(s)
Chlorides/metabolism , Colon/drug effects , Colon/metabolism , Flavanones , Flavonoids/pharmacology , 1-Methyl-3-isobutylxanthine/pharmacology , Amiloride/pharmacology , Animals , Atropine/pharmacology , Calcium/metabolism , Carbachol/pharmacology , Colforsin/pharmacology , Cyclic AMP/biosynthesis , Dinoprostone/pharmacology , Electric Conductivity , Female , Indomethacin/pharmacology , Intestinal Mucosa/drug effects , Male , Muscarinic Antagonists/pharmacology , Potassium Channel Blockers , Rats , Rats, Sprague-Dawley , Tetrodotoxin/pharmacology , Thapsigargin/pharmacology
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