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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
14
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pubmed:dateCreated |
1990-6-13
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pubmed:abstractText |
Transport of S-(2,4-dinitrophenyl)glutathione (DNP-SG), a model compound of glutathione S-conjugates, was studied in purified canalicular and basolateral (i.e. sinusoidal and lateral) rat liver plasma membrane (LPM) vesicles. Incubation of canalicular LPM vesicles with DNP-SG in the presence of ATP resulted in an uptake of DNP-SG into the vesicles. In contrast, in basolateral LPM vesicles the initial rate of ATP-dependent DNP-SG uptake was 3-4-fold lower than that of the canalicular LPM. This suggests that the ATP-dependent glutathione S-conjugates transport is localized in the canalicular membrane of the hepatocytes. The rate of DNP-SG uptake into canalicular LPM vesicles exhibited saturation kinetics with apparent Km values of 4 microM for DNP-SG and 260 microM for ATP. The DNP-SG uptake was inhibited by various glutathione S-conjugates and GSSG, not GSH. The bulkiness of S-substituent alkyl groups in the conjugates and cysteinylglycine of glutathione are essential for the inhibition. In contrast to the ATP-dependent process, the uptake of DNP-SG to basolateral LPM in the presence of KCl was 4-fold higher than that of canalicular LPM. The rate of DNP-SG uptake was enhanced by a valinomycin-induced K+ diffusion potential, and was inhibited by GSH. These results suggest that electrogenic transport of glutathione S-conjugates is localized in the basolateral membrane of the hepatocytes. These studies provide evidence that the ATP-dependent canalicular transport system functions in biliary secretion of glutathione S-conjugates.
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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/Adenosine Triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Chloride,
http://linkedlifedata.com/resource/pubmed/chemical/S-(2,4-dinitrophenyl)glutathione,
http://linkedlifedata.com/resource/pubmed/chemical/Valinomycin
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
265
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7737-41
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2335503-Adenosine Triphosphate,
pubmed-meshheading:2335503-Animals,
pubmed-meshheading:2335503-Bile Canaliculi,
pubmed-meshheading:2335503-Bile Ducts, Intrahepatic,
pubmed-meshheading:2335503-Biological Transport,
pubmed-meshheading:2335503-Cell Membrane,
pubmed-meshheading:2335503-Glutathione,
pubmed-meshheading:2335503-Kinetics,
pubmed-meshheading:2335503-Liver,
pubmed-meshheading:2335503-Male,
pubmed-meshheading:2335503-Potassium Chloride,
pubmed-meshheading:2335503-Rats,
pubmed-meshheading:2335503-Rats, Inbred Strains,
pubmed-meshheading:2335503-Valinomycin
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pubmed:year |
1990
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pubmed:articleTitle |
Mechanism of glutathione S-conjugate transport in canalicular and basolateral rat liver plasma membranes.
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pubmed:affiliation |
Institute of Scientific and Industrial Research, Osaka University, Japan.
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pubmed:publicationType |
Journal Article,
Comparative Study
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