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Vol. 27, Issue 8, 872-879, August 1999
Department of Pharmaceutics, College of Pharmacy, Seoul National
University, Seoul, Korea
Two structurally similar quaternary ammonium compounds,
triethylmethylammonium (TEMA, Mr 116)
and tributylmethylammonium (TBuMA, Mr 200)
were used as model compounds to identify the unit process of
hepatobiliary excretion that is responsible for markedly different biliary excretion of organic cations (OCs). Cumulative biliary excretion (in percentage of dose; i.v., 12 µmol/kg) was 0.17 for TEMA
and 34.5 for TBuMA. In vivo uptake clearance into the liver was
0.686 ± 0.020 ml/min for TEMA and 0.421 ± 0.028 ml/min for TBuMA. When the uptake clearance was examined in an isolated hepatocyte system, comparable clearance between TEMA and TBuMA was obtained, consistent with the in vivo result. These observations suggest that
uptake into the liver is not the major determinant for the difference
in biliary excretion of the OCs. Coadministration of colchicine, an
inhibitor of microtubule formation, had no effect on biliary excretion
of the model compounds, and the primary site of subcellular
distribution of the OCs appears to be the cytosol, suggesting that
intracellular movement does not play a major role in the markedly
different biliary excretion of the OCs. In contrast, in vivo excretion
clearance across the canalicular membrane for TBuMA was 180-fold
greater than that for TEMA, and in vitro efflux clearance of TBuMA was
smaller than that of TEMA (p < .01), indicative of
involvement of these processes in the markedly different biliary excretion of the OCs. Therefore, these data indicate that canalicular transport is primarily responsible for the markedly different biliary
excretion of TEMA and TBuMA.
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