Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1991-4-22
|
pubmed:abstractText |
Infection of MA-104 cells with the OSU strain of rotavirus induced an increase in Na+ and a decrease in K+ intracellular concentrations, starting at 4 h post-infection. These changes were not related to an inhibition of the Na+/K+ pump since ouabain-sensitive 86Rb uptake was augmented in rotavirus-infected cells compared to control cells, whereas the [3H]ouabain binding and Na+/K+ ATPase activity in the cell homogenate were unaffected. Furosemide-sensitive 86Rb uptake (Na+/K+/2Cl- cotransport) was not modified by the infection. Passive 86Rb efflux and 22Na influx were augmented in infected cells suggesting an increase in the plasma membrane permeability. The increase in intracellular Na+ concentration might be responsible for the observed stimulation of the Na+/K+ pump. This effect was dependent upon the synthesis of viral proteins because it was abolished by addition of cycloheximide up to 4 h post-infection. Prevention of the increase in intracellular Na+ by the use of low Na(+)-containing media did not modify the pattern of protein synthesis. This suggests that changes in intracellular Na+ and K+ concentrations were not related to shutoff of cellular protein synthesis. Alterations of ion contents in the rotavirus-infected enterocytes might impair intestinal absorptive capacity before the appearance of histopathological lesions.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cycloheximide,
http://linkedlifedata.com/resource/pubmed/chemical/Furosemide,
http://linkedlifedata.com/resource/pubmed/chemical/Ouabain,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium-Potassium-Exchanging ATPase,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0022-1317
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
72 ( Pt 3)
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
541-7
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1848590-Animals,
pubmed-meshheading:1848590-Biological Transport, Active,
pubmed-meshheading:1848590-Cell Line,
pubmed-meshheading:1848590-Cell Membrane Permeability,
pubmed-meshheading:1848590-Cycloheximide,
pubmed-meshheading:1848590-Furosemide,
pubmed-meshheading:1848590-Homeostasis,
pubmed-meshheading:1848590-Ouabain,
pubmed-meshheading:1848590-Potassium,
pubmed-meshheading:1848590-Rotavirus,
pubmed-meshheading:1848590-Sodium,
pubmed-meshheading:1848590-Sodium-Potassium-Exchanging ATPase,
pubmed-meshheading:1848590-Viral Proteins
|
pubmed:year |
1991
|
pubmed:articleTitle |
Rotavirus infection alters Na+ and K+ homeostasis in MA-104 cells.
|
pubmed:affiliation |
Laboratorio de Fisiología Gastrointestinal, Instituto Venezolano de Investigaciones Cientificas (IVIC), Caracas, Venezuela.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|