Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1999-1-19
|
pubmed:abstractText |
Pancreatic duct epithelial cells (PDECs) mediate the pancreatic secretion of fluid and electrolytes. Membrane K+ channels on these cells regulate intracellular K+ concentration; in combination with the Na+/H+ antiport and Na+,K+ adenosine triphosphatase (ATPase), they may also mediate serosal H+ secretion, balancing luminal HCO3- secretion. We describe the K+ conductances on well-differentiated and functional nontransformed cultured dog PDECs. Through 86Rb+ efflux studies, we demonstrated Ca(2+)-activated K+ channels that were stimulated by A23187, thapsigargin, and 1-ethyl-2-benzimidazolinone, but not forskolin. These conductances also were localized on the basolateral membrane because 86Rb+ efflux was directed toward the serosal compartment. Of the K+ channel blockers, BaCl2, charybdotoxin, clotrimazole, and quinidine, but not 4-aminopyridine, apamin, tetraethylammonium, or iberiotoxin, inhibited 86Rb+ efflux. This efflux was not inhibited by amiloride, ouabain, and bumetanide, inhibitors of the Na+/H+ antiport, the Na+,K(+)-ATPase pump, and the Na+,K+,2Cl- cotransporter, respectively. When apically permeabilized PDEC monolayers were mounted in Ussing chambers with a luminal-to-serosal K+ gradient, A23187 and 1-ethyl-2-benzimidazolinone stimulated a charybdotoxin-sensitive short-circuit current (Isc) increase. Characterization of K+ channels on these cultured PDECs, along with previous identification of Cl- channels (1), further supports the importance of these cells as models for pancreatic duct secretion.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1-ethyl-2-benzimidazolinone,
http://linkedlifedata.com/resource/pubmed/chemical/Benzimidazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Calcimycin,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Charybdotoxin,
http://linkedlifedata.com/resource/pubmed/chemical/Clotrimazole,
http://linkedlifedata.com/resource/pubmed/chemical/Forskolin,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Quinidine,
http://linkedlifedata.com/resource/pubmed/chemical/Rubidium Radioisotopes
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0885-3177
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
17
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
348-58
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9821176-Animals,
pubmed-meshheading:9821176-Benzimidazoles,
pubmed-meshheading:9821176-Calcimycin,
pubmed-meshheading:9821176-Calcium,
pubmed-meshheading:9821176-Calcium Channel Agonists,
pubmed-meshheading:9821176-Cell Membrane,
pubmed-meshheading:9821176-Cells, Cultured,
pubmed-meshheading:9821176-Charybdotoxin,
pubmed-meshheading:9821176-Clotrimazole,
pubmed-meshheading:9821176-Dogs,
pubmed-meshheading:9821176-Electric Conductivity,
pubmed-meshheading:9821176-Epithelial Cells,
pubmed-meshheading:9821176-Forskolin,
pubmed-meshheading:9821176-Pancreatic Ducts,
pubmed-meshheading:9821176-Potassium Channels,
pubmed-meshheading:9821176-Quinidine,
pubmed-meshheading:9821176-Rubidium Radioisotopes
|
pubmed:year |
1998
|
pubmed:articleTitle |
Calcium-activated potassium conductances on cultured nontransformed dog pancreatic duct epithelial cells.
|
pubmed:affiliation |
University of Washington, Seattle, USA. t1nguyen@u.washington.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
|