Literature DB >> 10227709

Different activity of ATP dependent transport across the canalicular membrane for tributylmethylammonium and triethylmethylammonium as a potential mechanism of the preferential biliary excretion for tributylmethylammonium in the rat.

I S Song1, S J Chung, C K Shim.   

Abstract

PURPOSE: The mechanism(s) responsible for the significantly higher biliary excretion of tributyl methyl ammonium (TBuMA) than of triethyl methyl ammonium (TEMA) was investigated in canalicular liver plasma membrane vesicles (cLPM).
METHODS: The uptake of [3H]TBuMA and [3H]TEMA into cLPM in the presence of a pH gradient or ATP was measured by a rapid filtration technique.
RESULTS: The uptake of substrates into the vesicle was significantly increased by an outwardly directed pH gradient. The pH dependent uptake was saturable and cross-inhibited by the other organic cation, indicating that TEMA and TBuMA share a common transport mechanism. Kinetic analysis revealed the two compounds show similar characteristics for the pH-gradient dependent uptake. Thus, the organic cation/H+ exchange mechanism does not appear to explain the significant difference in biliary excretion of the organic cations. In the presence of ATP, however, uptake into cLPM was readily observed for TBuMA while TEMA uptake was negligible. Inhibition studies with typical P-glycoprotein substrates indicated the uptake may be mediated by the P-glycoprotein.
CONCLUSIONS: Differences between TBuMA and TEMA in reactivity for an ATP dependent transport process, rather than for an organic cation/H+ exchanger, may be responsible for the markedly different biliary excretion of TBuMA and TEMA.

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Year:  1999        PMID: 10227709     DOI: 10.1023/a:1018823113314

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  23 in total

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Journal:  Br J Pharmacol       Date:  1998-02       Impact factor: 8.739

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Journal:  Biochem J       Date:  1973-12       Impact factor: 3.857

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Journal:  Biochem J       Date:  1973-12       Impact factor: 3.857

7.  Selective induction by phenobarbital of the electrogenic transport of glutathione and organic anions in rat liver canalicular membrane vesicles.

Authors:  J C Fernández-Checa; M Ookhtens; N Kaplowitz
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8.  Heterologous expression of various P-glycoproteins in polarized epithelial cells induces directional transport of small (type 1) and bulky (type 2) cationic drugs.

Authors:  J W Smit; B Weert; A H Schinkel; D K Meijer
Journal:  J Pharmacol Exp Ther       Date:  1998-07       Impact factor: 4.030

9.  Hepatobiliary and intestinal clearance of amphiphilic cationic drugs in mice in which both mdr1a and mdr1b genes have been disrupted.

Authors:  J W Smit; A H Schinkel; B Weert; D K Meijer
Journal:  Br J Pharmacol       Date:  1998-05       Impact factor: 8.739

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Journal:  J Biol Chem       Date:  1983-04-25       Impact factor: 5.157

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