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National Institute of Environmental Health Sciences

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Publication Detail

Title: Hepatic uptake of intact glutathione S-conjugate, inhibition by organic anions, and sinusoidal catabolism.

Authors: Hinchman, C A; Truong, A T; Ballatori, N

Published In Am J Physiol, (1993 Sep)

Abstract: To identify potential mechanisms for hepatic removal of circulating glutathione (GSH) conjugates, uptake and metabolism of S-2,4-dinitrophenylglutathione (DNP-SG) were examined in isolated perfused livers from rat and guinea pig. Guinea pig livers perfused with 5 mumol of DNP-SG in a recirculating system (50 microM initial concn) rapidly cleared the conjugate from the perfusate (half time 3.7 min), whereas clearance was considerably slower in rat liver (half time 35 min). Disappearance of DNP-SG from the perfusate was accompanied by a simultaneous appearance of DNP-SG and its metabolites in bile. Addition of acivicin, an inhibitor of gamma-glutamyltransferase (gamma-GT), to the perfusate resulted in a marked decrease in DNP-SG clearance by guinea pig liver but had no effect in rat liver, suggesting that in the guinea pig this process is largely dependent on sinusoidal gamma-GT activity. However, even in the presence of acivicin, rat and guinea pig livers removed nearly one-half of the administered DNP-SG from the recirculating perfusate over 30 min. High concentrations of DNP-SG were found in bile (up to 3.7 mM), indicating that the liver is capable of transporting the intact conjugate from the circulation. When rat livers were perfused with higher concentrations of DNP-SG (100 and 250 microM), biliary excretion of DNP-SG increased dose dependently, with concentrations in bile reaching 10 mM at the higher dose. This was accompanied by a dose-dependent choleresis.(ABSTRACT TRUNCATED AT 250 WORDS)

PubMed ID: 8105695 Exiting the NIEHS site

MeSH Terms: Animals; Cations/pharmacology*; Glutathione/analogs & derivatives*; Glutathione/antagonists & inhibitors; Glutathione/metabolism; Guinea Pigs; Isoxazoles/pharmacology; Liver/metabolism*; Male; Osmolar Concentration; Perfusion; Rats; gamma-Glutamyltransferase/antagonists & inhibitors; gamma-Glutamyltransferase/metabolism

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