INHIBITION OF ACETAMINOPHEN AND LORAZEPAM GLUCURONIDATION INVITRO BY PROBENECID

被引:24
作者
VONMOLTKE, LL
MANIS, M
HARMATZ, JS
POORMAN, R
GREENBLATT, DJ
机构
[1] TUFTS UNIV,SCH MED,DEPT PHARMACOL & EXPTL THERAPEUT,136 HARRISON AVE,BOSTON,MA 02111
[2] UPJOHN CO,KALAMAZOO,MI 49001
[3] NEW ENGLAND MED CTR,BOSTON,MA
关键词
INVITRO METABOLISM; GLUCURONIDE CONJUGATION; ACETAMINOPHEN; LORAZEPAM; PROBENECID INHIBITION;
D O I
10.1002/bdd.2510140204
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of probenecid on glucuronidation of acetaminophen and lorazepam in hepatic microsomes from various species was studied to see if in vitro results Were consistent with previous in vivo observations. Mouse, rat, and human microsomes were incubated with acetaminophen and probenecid while monkey microsomes were incubated with lorazepam and probenecid. Glucuronidation rates in all species varied with substrate, protein, and detergent concentrations. Mice exhibited faster rates of glucuronidation than rats or humans. All species showed inhibition of glucuronidation of acetaminophen or lorazepam when probenecid was added. Analysis suggested competitive inhibition. Thus, in vitro studies support in vivo results and confirm that the inhibition takes place at the hepatic level.
引用
收藏
页码:119 / 130
页数:12
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