A MODEL OF ISONIAZID-INDUCED HEPATOTOXICITY IN RABBITS

被引:61
|
作者
SARICH, TC
ZHOU, T
ADAMS, SP
BAIN, AI
WALL, RA
WRIGHT, JM
机构
[1] UNIV BRITISH COLUMBIA, FAC MED, DEPT PHARMACOL & THERAPEUT, VANCOUVER, BC V6T 1Z3, CANADA
[2] UNIV BRITISH COLUMBIA, FAC MED, DEPT MED, VANCOUVER, BC V6T 1Z3, CANADA
关键词
ISONIAZID; DRUG-INDUCED HEPATOTOXICITY; ARGININOSUCCINIC ACID LYASE; HEPATIC NECROSIS; CYTOCHROME P-450; PHENOBARBITAL;
D O I
10.1016/1056-8719(95)00044-I
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Isoniazid (INH) continues to be an effective drug used for chemoprophylaxis and treatment of tuberculosis. Unfortunately, INH is associated with significant hepatotoxicity in up to 2% of individuals exposed, and if this adverse event is not recognized early it can be fatal. Research on INH-induced hepatotoxicity has been hampered by the lack of a suitable animal model that closely resembles the toxicity in humans. The mechanism of INH-induced hepatotoxicity is still unknown. The present study describes the development of a reliable model of INH-induced hepatotoxicity in rabbits. The protocol involves repeated injections of INH over a 2-day period, resulting in significant hepatic necrosis as indicated by elevations of plasma argininosuccinic acid lyase activity. Pretreatment with phenobarbital increased the occurrence of INH-induced hepatic necrosis from approximately 60% (9 out of 15 rabbits) with INH alone to more than 90% (13 out of 14 rabbits). Morphological indices were used to demonstrate the presence of INH-induced hepatotoxicity, and biochemical indices were used to demonstrate both the presence and severity of INH-induced hepatotoxicity in this model. This model may prove useful for further investigations into the mechanism of INH-induced hepatotoxicity.
引用
收藏
页码:109 / 116
页数:8
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