Cypermethrin and beta-cyfl uthrin are two most widely used multipurpose pyrethroids. After determining their oral LD 50 (416.98 mg kg -1 and 354.8 mg kg -1 body weight, respectively), we assessed their hepatotoxicity in Wistar rats following acute (0.1 LD 50 for 1 day) and sub-acute (0.1 LD 50 for 7, 14, 21 or 28 days) poisoning. The assessment was based on hepatic marker enzymes AST, ALT, LDH, ALP, glycogen, total proteins, total lipids, cholesterol, free fatty acids, and phospholipids. AST, ALT, LDH, total lipids, cholesterol, phospholipids, and free fatty acids in hepatic homogenate increased following pyrethroid stress. In contrast, hepatic proteins, glycogen, and ALP activity decreased due to lysis of structural proteins and leakage of enzymes into the blood stream. Biochemical data were consistent with histological alterations (cytoplasmic vacuolisation, nuclear polymorphism, eccentric nucleus, karyolysis, karyorrhexis, and sinusoidal dilation). Comparatively greater hepatocellular damage was noted in beta-cyfl uthrin than in cypermethrin-treated rats, which is probably related to the fl uorine atom in beta-cyfl uthrin.