rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1-2
|
pubmed:dateCreated |
1996-1-17
|
pubmed:abstractText |
The hypothesis that P-glycoprotein (P-gp) mediates the renal secretion of organic cations was tested by functional expression of mRNAs in the Xenopus laevis oocyte system. Efflux of 2'-deoxytubercidin (dTub), a substrate for the renal organic cation transporter (OCT) but not for P-gp, was enhanced by injection of renal mRNA but not by injection of mRNA from P-gp-overexpressing cells (MDCK cells transduced with the cDNA for human MDR1). The functional capacity of the MDCK-MDR mRNA was established by its ability to reduce the steady-state uptake of a classical P-gp substrate, vinblastine. Thus, these data indicate OCT and P-gp to be distinct entities. The Xenopus oocyte system provides a functional approach to further characterize the OCT.
|
pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0344-5704
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
37
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
187-9
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:7497591-Animals,
pubmed-meshheading:7497591-Biological Transport,
pubmed-meshheading:7497591-Carrier Proteins,
pubmed-meshheading:7497591-Cations,
pubmed-meshheading:7497591-Female,
pubmed-meshheading:7497591-Humans,
pubmed-meshheading:7497591-Ion Transport,
pubmed-meshheading:7497591-Kidney,
pubmed-meshheading:7497591-Mice,
pubmed-meshheading:7497591-Oocytes,
pubmed-meshheading:7497591-P-Glycoprotein,
pubmed-meshheading:7497591-RNA, Messenger,
pubmed-meshheading:7497591-Swine,
pubmed-meshheading:7497591-Tubercidin,
pubmed-meshheading:7497591-Xenopus laevis
|
pubmed:year |
1995
|
pubmed:articleTitle |
Functional expression of the renal organic cation transporter and P-glycoprotein in Xenopus laevis oocytes.
|
pubmed:affiliation |
Department of Experimental Pediatrics, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|