Curcumin Stimulates Cystic Fibrosis Transmembrane Conductance Regulator Clâ Channel Activity
Compounds that enhance either the function or biosynthetic processing of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl â channel may be of value in developing new treatments for cystic fibrosis (CF). Previous studies suggested that the herbal extract curcumin might affect the p...
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Veröffentlicht in: | The Journal of biological chemistry 2005-02, Vol.280 (7), p.5221 |
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container_title | The Journal of biological chemistry |
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creator | Allan L. Berger Christoph O. Randak Lynda S. Ostedgaard Philip H. Karp Daniel W. Vermeer Michael J. Welsh |
description | Compounds that enhance either the function or biosynthetic processing of the cystic fibrosis transmembrane conductance regulator
(CFTR) Cl â channel may be of value in developing new treatments for cystic fibrosis (CF). Previous studies suggested that the herbal
extract curcumin might affect the processing of a common CF mutant, CFTR-ÎF508. Here, we tested the hypothesis that curcumin
influences channel function. Curcumin increased CFTR channel activity in excised, inside-out membrane patches by reducing
channel closed time and prolonging the time channels remained open. Stimulation was dose-dependent, reversible, and greater
than that observed with genistein, another compound that stimulates CFTR. Curcumin-dependent stimulation required phosphorylated
channels and the presence of ATP. We found that curcumin increased the activity of both wild-type and ÎF508 channels. Adding
curcumin also increased Cl â transport in differentiated non-CF airway epithelia but not in CF epithelia. These results suggest that curcumin may directly
stimulate CFTR Cl â channels. |
doi_str_mv | 10.1074/jbc.M412972200 |
format | Article |
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(CFTR) Cl â channel may be of value in developing new treatments for cystic fibrosis (CF). Previous studies suggested that the herbal
extract curcumin might affect the processing of a common CF mutant, CFTR-ÎF508. Here, we tested the hypothesis that curcumin
influences channel function. Curcumin increased CFTR channel activity in excised, inside-out membrane patches by reducing
channel closed time and prolonging the time channels remained open. Stimulation was dose-dependent, reversible, and greater
than that observed with genistein, another compound that stimulates CFTR. Curcumin-dependent stimulation required phosphorylated
channels and the presence of ATP. We found that curcumin increased the activity of both wild-type and ÎF508 channels. Adding
curcumin also increased Cl â transport in differentiated non-CF airway epithelia but not in CF epithelia. These results suggest that curcumin may directly
stimulate CFTR Cl â channels.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M412972200</identifier><identifier>PMID: 15582996</identifier><language>eng</language><publisher>American Society for Biochemistry and Molecular Biology</publisher><ispartof>The Journal of biological chemistry, 2005-02, Vol.280 (7), p.5221</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Allan L. Berger</creatorcontrib><creatorcontrib>Christoph O. Randak</creatorcontrib><creatorcontrib>Lynda S. Ostedgaard</creatorcontrib><creatorcontrib>Philip H. Karp</creatorcontrib><creatorcontrib>Daniel W. Vermeer</creatorcontrib><creatorcontrib>Michael J. Welsh</creatorcontrib><title>Curcumin Stimulates Cystic Fibrosis Transmembrane Conductance Regulator Clâ Channel Activity</title><title>The Journal of biological chemistry</title><description>Compounds that enhance either the function or biosynthetic processing of the cystic fibrosis transmembrane conductance regulator
(CFTR) Cl â channel may be of value in developing new treatments for cystic fibrosis (CF). Previous studies suggested that the herbal
extract curcumin might affect the processing of a common CF mutant, CFTR-ÎF508. Here, we tested the hypothesis that curcumin
influences channel function. Curcumin increased CFTR channel activity in excised, inside-out membrane patches by reducing
channel closed time and prolonging the time channels remained open. Stimulation was dose-dependent, reversible, and greater
than that observed with genistein, another compound that stimulates CFTR. Curcumin-dependent stimulation required phosphorylated
channels and the presence of ATP. We found that curcumin increased the activity of both wild-type and ÎF508 channels. Adding
curcumin also increased Cl â transport in differentiated non-CF airway epithelia but not in CF epithelia. These results suggest that curcumin may directly
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(CFTR) Cl â channel may be of value in developing new treatments for cystic fibrosis (CF). Previous studies suggested that the herbal
extract curcumin might affect the processing of a common CF mutant, CFTR-ÎF508. Here, we tested the hypothesis that curcumin
influences channel function. Curcumin increased CFTR channel activity in excised, inside-out membrane patches by reducing
channel closed time and prolonging the time channels remained open. Stimulation was dose-dependent, reversible, and greater
than that observed with genistein, another compound that stimulates CFTR. Curcumin-dependent stimulation required phosphorylated
channels and the presence of ATP. We found that curcumin increased the activity of both wild-type and ÎF508 channels. Adding
curcumin also increased Cl â transport in differentiated non-CF airway epithelia but not in CF epithelia. These results suggest that curcumin may directly
stimulate CFTR Cl â channels.</abstract><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>15582996</pmid><doi>10.1074/jbc.M412972200</doi></addata></record> |
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title | Curcumin Stimulates Cystic Fibrosis Transmembrane Conductance Regulator Clâ Channel Activity |
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