Source:http://linkedlifedata.com/resource/pubmed/id/18752001
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2009-2-9
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pubmed:abstractText |
Previous in vitro studies suggested that Cl(-) currents produced by the cystic fibrosis transmembrane conductance regulator (CFTR; ABCC7) are inhibited by the alpha1 isoform of the adenosine monophosphate (AMP)-stimulated kinase (AMPK). AMPK is a serine/threonine kinase that is activated during metabolic stress. It has been proposed as a potential mediator for transport-metabolism coupling in epithelial tissues. All previous studies have been performed in vitro and thus little is known about the regulation of Cl(-) secretion by AMPK in vivo. Using AMPKalpha1(-/-) mice and wild-type littermates, we demonstrate that phenformin, an activator of AMPK, strongly inhibits cAMP-activated Cl(-) secretion in mouse airways and colon, when examined in ex vivo in Ussing chamber recordings. However, phenformin was equally effective in AMPKalpha1(-/-) and wild-type animals, suggesting additional AMPK-independent action of phenformin. Phenformin inhibited CFTR Cl(-) conductance in basolaterally permeabilized colonic epithelium from AMPKalpha1(+/+) but not AMPKalpha1(-/-) mice. The inhibitor of AMPK compound C enhanced CFTR-mediated Cl(-) secretion in epithelial tissues of AMPKalpha1(-/-) mice, but not in wild-type littermates. There was no effect on Ca(2+)-mediated Cl(-) secretion, activated by adenosine triphosphate or carbachol. Moreover CFTR-dependent Cl(-) secretion was enhanced in the colon of AMPKalpha1(-/-) mice, as indicated in Ussing chamber ex vivo and rectal PD measurements in vivo. Taken together, these data suggest that epithelial Cl(-) secretion mediated by CFTR is controlled by AMPK in vivo.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/(6-(4-(2-piperidin-1-ylethoxy)phenyl...,
http://linkedlifedata.com/resource/pubmed/chemical/AMP-Activated Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Chlorides,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP,
http://linkedlifedata.com/resource/pubmed/chemical/Cystic Fibrosis Transmembrane...,
http://linkedlifedata.com/resource/pubmed/chemical/Phenformin,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidines
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1432-2013
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
457
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1071-8
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pubmed:meshHeading |
pubmed-meshheading:18752001-AMP-Activated Protein Kinases,
pubmed-meshheading:18752001-Animals,
pubmed-meshheading:18752001-Chlorides,
pubmed-meshheading:18752001-Colon,
pubmed-meshheading:18752001-Cyclic AMP,
pubmed-meshheading:18752001-Cystic Fibrosis Transmembrane Conductance Regulator,
pubmed-meshheading:18752001-Epithelium,
pubmed-meshheading:18752001-Mice,
pubmed-meshheading:18752001-Mice, Knockout,
pubmed-meshheading:18752001-Phenformin,
pubmed-meshheading:18752001-Pyrazoles,
pubmed-meshheading:18752001-Pyrimidines
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pubmed:year |
2009
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pubmed:articleTitle |
Regulation of Cl(-) secretion by AMPK in vivo.
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pubmed:affiliation |
Department of Physiology, University of Regensburg, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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