A number of studies have shown that interaction of certain combinations of pesticides can lead to enhancement of toxicity. In view of this, acute interactive effects of lindane and dimethoate were studied in rats randomized into four groups of six each. The first group was treated with lindane p.o. 10 mg/kg, the second group was treated with dimethoate p.o. 20 mg/kg, the third group was given dimethoate p.o. 20 mg/kg to rats pretreated (one hour before) with lindane p.o. 10 mg/kg and the fourth group serving as control was given oil only. The animals were sacrificed one hour after the exposure to determine the brain cortex and corpus striatum acetylcholinesterase (AChE) activity, blood glucose level, glycogen content in cerebral and peripheral tissues and free ammonia level in the brain. There was a si gnificantly greater inhibition of brain cortex and corpus striatum AChE activity ( p<0.001) and enhancement of effect on free ammonia level in the brain of rats ( p<0.05) dosed with lindane þ dimethoate than in rats treated either with lindane or dimethoate. The hyperglycemic action of both lindane and dimethoate when given alone was off-set in the group treated with both lindane and dimethoate ( p<0.05 and 0.001 respectively). Further, treatments with dimethoate of rats pretreated with lindane antagonised the effect of lindane on glycogen content in liver, brain and triceps ( p<0.05) but not in the diaphragm. The study signifies the importance of co-exposure in the risk assessment of chemicals in the environment laden with xenobiotics.