Stimulation of chloride secretion by baicalein in isolated rat distal colon
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...
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Veröffentlicht in: | American journal of physiology: Gastrointestinal and liver physiology 2002-03, Vol.282 (3), p.G508-G518 |
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creator | Ko, W H Law, V W Y Yip, W C Y Yue, G G L Lau, C W Chen, Z Y Huang, Y |
description | 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. |
doi_str_mv | 10.1152/ajpgi.00291.2001 |
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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.</description><identifier>ISSN: 0193-1857</identifier><identifier>EISSN: 1522-1547</identifier><identifier>DOI: 10.1152/ajpgi.00291.2001</identifier><identifier>PMID: 11842001</identifier><language>eng</language><publisher>United States</publisher><subject>1-Methyl-3-isobutylxanthine - pharmacology ; Amiloride - pharmacology ; Animals ; Atropine - pharmacology ; Calcium - metabolism ; Carbachol - pharmacology ; Chlorides - metabolism ; Colforsin - pharmacology ; Colon - drug effects ; Colon - secretion ; Cyclic AMP - biosynthesis ; Dinoprostone - pharmacology ; Electric Conductivity ; Female ; Flavanones ; Flavonoids - pharmacology ; Indomethacin - pharmacology ; Intestinal Mucosa - drug effects ; Male ; Muscarinic Antagonists - pharmacology ; Potassium Channel Blockers ; Rats ; Rats, Sprague-Dawley ; Tetrodotoxin - pharmacology ; Thapsigargin - pharmacology</subject><ispartof>American journal of physiology: Gastrointestinal and liver physiology, 2002-03, Vol.282 (3), p.G508-G518</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c295t-568b591a40ec645345b898aa395bea25f0301942a67fc8b4fd494cebf5001d923</citedby><cites>FETCH-LOGICAL-c295t-568b591a40ec645345b898aa395bea25f0301942a67fc8b4fd494cebf5001d923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11842001$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ko, W H</creatorcontrib><creatorcontrib>Law, V W Y</creatorcontrib><creatorcontrib>Yip, W C Y</creatorcontrib><creatorcontrib>Yue, G G L</creatorcontrib><creatorcontrib>Lau, C W</creatorcontrib><creatorcontrib>Chen, Z Y</creatorcontrib><creatorcontrib>Huang, Y</creatorcontrib><title>Stimulation of chloride secretion by baicalein in isolated rat distal colon</title><title>American journal of physiology: Gastrointestinal and liver physiology</title><addtitle>Am J Physiol Gastrointest Liver Physiol</addtitle><description>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.</description><subject>1-Methyl-3-isobutylxanthine - pharmacology</subject><subject>Amiloride - pharmacology</subject><subject>Animals</subject><subject>Atropine - pharmacology</subject><subject>Calcium - metabolism</subject><subject>Carbachol - pharmacology</subject><subject>Chlorides - metabolism</subject><subject>Colforsin - pharmacology</subject><subject>Colon - drug effects</subject><subject>Colon - secretion</subject><subject>Cyclic AMP - biosynthesis</subject><subject>Dinoprostone - pharmacology</subject><subject>Electric Conductivity</subject><subject>Female</subject><subject>Flavanones</subject><subject>Flavonoids - pharmacology</subject><subject>Indomethacin - pharmacology</subject><subject>Intestinal Mucosa - drug effects</subject><subject>Male</subject><subject>Muscarinic Antagonists - pharmacology</subject><subject>Potassium Channel Blockers</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Thapsigargin - pharmacology</subject><issn>0193-1857</issn><issn>1522-1547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEFLAzEQhYMotlbvniR_YOtMNmk3RylaxYIH9bxMsommbJuSbA_99-62BWFg4PHe8OZj7B5hiqjEI613P2EKIDROBQBesHEviwKVnF-yMaAuC6zUfMRucl4DgBKI12yEWMnBP2bvn13Y7FvqQtzy6Ln9bWMKjePZ2eSOqjlwQ8FS68KWD5Nj73cNT9TxJuSOWm5jG7e37MpTm93deU_Y98vz1-K1WH0s3xZPq8IKrbpCzSqjNJIEZ2dSlVKZSldEpVbGkVAeyr64FDSbe1sZ6RuppXXGq75xo0U5YXC6a1PMOTlf71LYUDrUCPXApT5yqY9c6uHPPvJwiuz2ZuOa_8AZRPkHh9RfIQ</recordid><startdate>20020301</startdate><enddate>20020301</enddate><creator>Ko, W H</creator><creator>Law, V W Y</creator><creator>Yip, W C Y</creator><creator>Yue, G G L</creator><creator>Lau, C W</creator><creator>Chen, Z Y</creator><creator>Huang, Y</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20020301</creationdate><title>Stimulation of chloride secretion by baicalein in isolated rat distal colon</title><author>Ko, W H ; Law, V W Y ; Yip, W C Y ; Yue, G G L ; Lau, C W ; Chen, Z Y ; Huang, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c295t-568b591a40ec645345b898aa395bea25f0301942a67fc8b4fd494cebf5001d923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>1-Methyl-3-isobutylxanthine - pharmacology</topic><topic>Amiloride - pharmacology</topic><topic>Animals</topic><topic>Atropine - pharmacology</topic><topic>Calcium - metabolism</topic><topic>Carbachol - pharmacology</topic><topic>Chlorides - metabolism</topic><topic>Colforsin - pharmacology</topic><topic>Colon - drug effects</topic><topic>Colon - secretion</topic><topic>Cyclic AMP - biosynthesis</topic><topic>Dinoprostone - pharmacology</topic><topic>Electric Conductivity</topic><topic>Female</topic><topic>Flavanones</topic><topic>Flavonoids - pharmacology</topic><topic>Indomethacin - pharmacology</topic><topic>Intestinal Mucosa - drug effects</topic><topic>Male</topic><topic>Muscarinic Antagonists - pharmacology</topic><topic>Potassium Channel Blockers</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Thapsigargin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ko, W H</creatorcontrib><creatorcontrib>Law, V W Y</creatorcontrib><creatorcontrib>Yip, W C Y</creatorcontrib><creatorcontrib>Yue, G G L</creatorcontrib><creatorcontrib>Lau, C W</creatorcontrib><creatorcontrib>Chen, Z Y</creatorcontrib><creatorcontrib>Huang, Y</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>American journal of physiology: Gastrointestinal and liver physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ko, W H</au><au>Law, V W Y</au><au>Yip, W C Y</au><au>Yue, G G L</au><au>Lau, C W</au><au>Chen, Z Y</au><au>Huang, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stimulation of chloride secretion by baicalein in isolated rat distal colon</atitle><jtitle>American journal of physiology: Gastrointestinal and liver physiology</jtitle><addtitle>Am J Physiol Gastrointest Liver Physiol</addtitle><date>2002-03-01</date><risdate>2002</risdate><volume>282</volume><issue>3</issue><spage>G508</spage><epage>G518</epage><pages>G508-G518</pages><issn>0193-1857</issn><eissn>1522-1547</eissn><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.</abstract><cop>United States</cop><pmid>11842001</pmid><doi>10.1152/ajpgi.00291.2001</doi></addata></record> |
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subjects | 1-Methyl-3-isobutylxanthine - pharmacology Amiloride - pharmacology Animals Atropine - pharmacology Calcium - metabolism Carbachol - pharmacology Chlorides - metabolism Colforsin - pharmacology Colon - drug effects Colon - secretion Cyclic AMP - biosynthesis Dinoprostone - pharmacology Electric Conductivity Female Flavanones Flavonoids - pharmacology Indomethacin - pharmacology Intestinal Mucosa - drug effects Male Muscarinic Antagonists - pharmacology Potassium Channel Blockers Rats Rats, Sprague-Dawley Tetrodotoxin - pharmacology Thapsigargin - pharmacology |
title | Stimulation of chloride secretion by baicalein in isolated rat distal colon |
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