Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1990-2-5
|
pubmed:abstractText |
Proximal duodenum from the amphibian Necturus was stripped of muscle layers and the mucosa was mounted as a tube for studies of alkali transport or as a flat sheet for intracellular impalement by voltage-sensitive glass micro-electrodes. The mucosa alkalinized the unbuffered luminal perfusate at a high rate (3.4 muequiv. cm-1 h-1) and developed a transepithelial electric potential difference of 5.7 mV (lumen negative). Transport was inhibited by 2,4-dinitrophenol (10(-4) M) and by furosemide (10(-3) M) and SITS (10(-3) M) on the seros but not on the mucosal side, indicating dependence on tissue metabolism and on serosal membrane Cl-/HCO3- exchange. Prostaglandin E2 (10(-7)-10(-5) M) and dibutyryl cyclic AMP (10(-6)-10(-4) M) had no effects on the secretion or transepithelial electrical potential difference. removal of serosal HCO3- decreased luminal alkalinization by 75%, indicating a contribution by passive migration of HCO3- and/or a dependence of transcellular transport on the nutrient supply of this ion. Administration of HCO3- (17.8 mM) to the luminal perfusate affected neither the transepithelial nor transmembrane electrical potential differences nor the resistance ratio. It is thus unlikely that the luminal membrane possesses any major HCO3- conductance.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2,4-Dinitrophenol,
http://linkedlifedata.com/resource/pubmed/chemical/Bicarbonates,
http://linkedlifedata.com/resource/pubmed/chemical/Bucladesine,
http://linkedlifedata.com/resource/pubmed/chemical/Dinitrophenols,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Furosemide,
http://linkedlifedata.com/resource/pubmed/chemical/Indomethacin,
http://linkedlifedata.com/resource/pubmed/chemical/Uncoupling Agents
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0001-6772
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
137
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
481-7
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2557727-2,4-Dinitrophenol,
pubmed-meshheading:2557727-Action Potentials,
pubmed-meshheading:2557727-Animals,
pubmed-meshheading:2557727-Bicarbonates,
pubmed-meshheading:2557727-Bucladesine,
pubmed-meshheading:2557727-Dinitrophenols,
pubmed-meshheading:2557727-Dinoprostone,
pubmed-meshheading:2557727-Duodenum,
pubmed-meshheading:2557727-Furosemide,
pubmed-meshheading:2557727-Indomethacin,
pubmed-meshheading:2557727-Intestinal Mucosa,
pubmed-meshheading:2557727-Necturus maculosus,
pubmed-meshheading:2557727-Uncoupling Agents
|
pubmed:year |
1989
|
pubmed:articleTitle |
Alkaline secretion by Necturus proximal duodenal mucosa.
|
pubmed:affiliation |
Department of Physiology and Medical Biophysics, Uppsala University Biomedical Centre, Sweden.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|