Korean J Intern Med.
1999 Jul;14(2):27-33.
TProtective effect of chlormethiazole, a sedative, against acetaminophen-induced
liver injury in mice
- Affiliations
-
- 1Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.
- 2Department of Anatomy, Ewha Womans University College of Medicine, Seoul, Korea.
Abstract
OBJECTIVES
The hepatotoxicity of acetaminophen is not a result of the parent
compound but is mediated by its reactive metabolite N-acetyl-p-benzoquinone
imine. Cytochrome P4502E1 (CYP2E1) is the principal enzyme of this
biotransformation, which accounts for approximately 52% of the bioactivation in
human microsomes. Recently, chlormethiazole a sedative drug, is reported to be
an efficient inhibitor of CYP2E1 activity in human beings. In this study we
wished to evaluate whether chlormethiazole, an inhibitor of CYP2E1, could
prevent acetaminophen-induced liver injury in mice. METHODS: Acetaminophen, at
doses ranging from 200 to 600 mg/kg, was injected into the peritoneum of female
C57BL/6 inbred mice fasted for four hours. Chlormethiazole (60 mg/kg) or 5%
dextrose water was given 30 min before or 2 h after acetaminophen. Serum
aminotransferase activities, histologic index score, survival rate and hepatic
malondialdehyde levels were compared. RESULTS: Pretreatment with chlormethiazole
30 min before 400 mg/kg of acetaminophen completely inhibited
acetaminophen-induced liver injury (median 118.5 U/L, range 75 to 142 vs. 14,070
U/L, range 5980 to 27,680 for AST; 49 U/L, range 41 to 64 vs. 15,330 U/L, range
13,920 to 15,940 for ALT). In mice receiving chlormethiazole 2 h after
acetaminophen, the mean AST and ALT levels were also less elevated, reaching
only 20% of the value of acetaminophen-only group. These protective effects were
confirmed histologically. Whereas more than 50% of mice died at 500 mg/kg of
acetaminophen, all the mice pretreated with chlormethiazole survived at the same
dose. CONCLUSION: Chlormethiazole effectively reduces acetaminophen-induced
liver injury in mice. Further studies are needed to assess its role in humans.