Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/14411
Type: Journal article
Title: Disposition of gemfibrozil and gemfibrozil acyl glucuronide in the rat isolated perfused liver
Author: Sallustio, B.
Fairchild, B.
Shanahan, K.
Evans, A.
Nation, R.
Citation: Drug Metabolism and Disposition, 1996; 24(9):984-989
Publisher: WILLIAMS & WILKINS
Issue Date: 1996
ISSN: 0090-9556
1521-009X
Statement of
Responsibility: 
Benedetta C. Sallustio, Barbara A. Fairchild, Kathryn Shanahan, Allan M. Evans, and Roger L. Nation
Abstract: Acyl glucuronides are reactive electrophilic metabolites and in vivo are readily hydrolyzed, undergo intramolecular rearrangement, and bind covalently to proteins. The isolated perfused liver preparation, using male Sprague-Dawley rats, was used to examine the hepatic disposition of the fibrate hypolipidemic agent gemfibrozil and its acyl glucuronide metabolite, 1-O-gemfibrozil-beta-D-glucuronide. Using a recirculating design, erythrocyte-free perfusion medium containing 1% (w/v) albumin was delivered to the liver via the portal vein at a flow rate of 30 ml/min, and for each experiment was spiked with either gemfibrozil (N = 4) or 1-O-gemfibrozil-beta-D-glucuronide (N = 4) at initial concentrations of 120 microM and 21 microM, respectively. In the gemfibrozil perfusions, the mean (SD) total perfusate clearance, half-life, hepatic extraction ratio of gemfibrozil, and the fraction of eliminated gemfibrozil excreted in bile as the glucuronide conjugate were 2.73 (0.30) ml/min, 76.9 (5.6) min, 0.091 (0.012), and 0.347 (0.154), respectively. In the 1-O-gemfibrozil-beta-D-glucuronide perfusions, the mean (SD) total perfusate clearance, half-life, hepatic extraction ratio, and fraction excreted in bile as the glucuronide conjugate were 19.5 (2.1) ml/min, 8.7 (0.9) min, 0.649 (0.068), and 0.534 (0.077), respectively. The higher hepatic extraction ratio for 1-O-gemfibrozil-beta-D-glucuronide could mostly be attributed to its higher unbound fraction in perfusate (0.182), compared with that of the parent drug (0.004), because the conjugate had a lower intrinsic clearance (305 ml/min) compared with the aglycone (751 ml/min). Control perfusions, conducted in the absence of a liver, showed negligible degradation of 1-O-gemfibrozil-beta-D-glucuronide over 90 min. However, in the presence of a liver, approximately 25% of 1-O-gemfibrozil-beta-D-glucuronide added to perfusate was hydrolyzed to gemfibrozil over 90 min. The study demonstrates the importance of the liver in the formation, uptake, hydrolysis, and excretion of 1-O-gemfibrozil-beta-D-glucuronide.
Keywords: Liver; Bile; Animals; Rats; Rats, Sprague-Dawley; Gemfibrozil; Glucuronates; Perfusion; Kinetics; Male; Hypolipidemic Agents
Rights: Copyright © 1996 by The American Society for Pharmacology and Experimental Therapeutics
RMID: 0030003413
Published version: http://dmd.aspetjournals.org/content/24/9/984.abstract
Appears in Collections:Pharmacology publications

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