Prallethrin induced serum biochemical changes in Wistar rats

The present study was designed as a repeated dose 28-day oral toxicity study in rodent. All the rats were randomly divided into five groups (C1, C2, T1, T2 and T3) each containing 10 Wistar rats (5 male and 5 female). Group C1 served as control as no treatment was administered. Group C2 was administered groundnut oil (1 ml/100 g b.wt) and served as vehicle control. Group T1 was put on high dose 153.33 mg/kg b.wt (LD50/3), while group T2 received intermediate dose of 92 mg/kg b.wt (LD50/5), and group T3 was administered low dose of 46 mg/kg b.wt (LD50/10) of Prallethrin suspended in 1 ml/100 g b.wt of groundnut oil. Blood samples were collected from all groups on the 7th, 14th, 21st and 28th day of the experiment for measurement of serum glucose, serum urea, serum triglyceride, serum cholesterol, serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT) and serum alkaline phosphatase (ALP). According to data obtained on the 7th day of the study, no statistically significant change in any of the treatment groups was observed as compared to the control group. On the 14th day of the study, in comparison to the control group, triglyceride level and ALP activity were found to be significantly increased in the group T1 female and group T1 male rats respectively. On the 21st day of the study, compared to the controls, significant increase in cholesterol and ALP levels were present in both T1 and T2 females and in addition to this total protein and triglycerides levels were also significantly increased in group T1 female rats. In group T1 male total protein, triglycerides, ALT and ALP activity was found to be increased significantly as compared to healthy control group. On the 28th day, all the recorded biochemical parameters were found to be significantly increased, except BUN and AST in group T1 female rats. In group T2 female rats, significantly increased cholesterol, ALT and ALP levels were observed. In group T3 female rats, none of the parameters were found to be significantly affected. Among male rats, only total protein level was found to be increased in groups T2 and T3. Whereas, total protein, triglyceride, ALT and ALP were significantly elevated in group T1 male rats at the end of the study. In conclusion, the results of this study demonstrate that subacute oral administration of Prallethrin; at dose levels of 1/3 LD50 and 1/5 LD50 for 28 days induces moderate toxic effects on different biochemical parameters.

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► Female rats were more susceptible to toxic effects of Prallethrin than male rats, at different dose levels.
► Majority of the studied parameters got significantly elevated at the end of fourth week.
► Elevated biochemical parameters correlated well with the histopathological changes in various vital organs.