Triazophos-induced oxidative stress and histomorphological changes in ovary of female Wistar rats.

Triazophos (TZ), a non-systemic broad spectrum organophosphate (OP), is being extensively used against a wide range of pests in agricultural practices. The present study was carried out to investigate the toxic effects of triazophos (TZ) in female Wistar rats. Three sub-chronic dose levels of TZ corresponding to 1/10th, 1/20th and 1/40th of LD50 were given for 30 days to adult female Wistar rats through oral intubation. During the treatment period estrous cycle was significantly altered. Activity levels of different oxidative stress (OS) parameters viz. catalase (CAT), superoxide dismutase (SOD), glutathione-S-transferase (GST), glutathione reductase (GR), glutathione peroxidase (GPx) and lipid peroxidation (LPO) were differentially altered in the ovary of treated rats. Estradiol levels were significantly high while progesterone levels were significantly reduced in plasma of 1/10th and 1/20th of LD50 TZ-treated rats. Histomorphological studies of ovary revealed increased follicular atresia and increased ovarian surface epithelial height in 1/10th and 1/20th of LD50 TZ-treated rats. Enhanced apoptosis and necrosis were also observed in ovarian granulosa cells at dose-dependent manner. Results infer that TZ exposure may lead to the number of pathophysiological conditions in female rats and severity increases at high doses.

A Three Generation Study with Effect of Imidacloprid in Rats: Biochemical and Histopathological Investigation.

OBJECTIVES: This study was designed to evaluate the dose-dependent toxic effects of imidacloprid on the female ratsthat were treated through three generations (F0, F1, and F2). F2 female rats were sacrificed at the end of the experiment to see the long-term effect of imidacloprid. MATERIALS AND METHODS: Rats were divided into three groups of 6 each. Group I served as control. Group II served as treated I and given 1/45(th) LD50 (10 mg/kg/day) of imidacloprid. Group III served as treated II and given 1/22(th) LD50 (20 mg/kg/day) of imidacloprid. After 60 days, oral administration of imidacloprid females were mated with normal males to get F1 and F2 generation. F2 generation female rats were sacrificed at the end of the experiment. Biochemical and a histopathological investigation was done for three groups of F2 generation and statistically analyzed by ANOVA. RESULTS: Average feed intake of F2 female rats was significantly reduced (P < 0.01) at 20 mg/kg/day dose of imidacloprid. There was a significant increase in the activity of alanine aminotransferase, AKP, and glucose 6-phosphate dehydrogenase in Group III rats of F2 generation. There was a significant decrease in acetylcholine esterase activity in plasma and brain of both the imidacloprid treated groups. Tissue samples of liver, kidney, and brain of females of F2 generation showed histopathological condition. CONCLUSION: The results indicated that imidacloprid at a dose of 20 mg/kg bw/day exerts significant toxicological effects on biochemical and histological studies of F2 generation females as compare to 10 mg/kg bw/day.

Physiological, biochemical and histological alterations induced by administration of imidacloprid in female albino rats.

Imidacloprid, a neonicotinoid the newest class of major insecticide has outstanding potency and systemic action for crop protection against piercing and sucking insects pests and also highly effective for control of flea on cats and dogs. The effect of oral administration of two doses of imidacloprid 10 and 20mg/kg/day for 60 days on biochemical parameters, histopathology and protein profile of female albino rat was assessed. Average feed intake was significantly reduced (P<0.01) at 20mg/kg/day. Relative weight of heart and spleen decreased significantly (P<0.05) at higher dose level. Non significant increase in alanine aminotransferase (ALT), aspartate aminotransferase (AST), acid phosphatase (ACP), alkaline phosphatase (AKP) activity was observed in both the imidacloprid treated groups. There was significant decrease (P<0.01, P<0.05) in acetyl cholinesterase (AChE) activity in plasma and brain of both the imidacloprid treated groups. Microscopically, liver tissue of rats treated with higher dose of imidacloprid showed marked dilation and congestion of central vein and degeneration of hepatocytes. The exposure to imidacloprid produced histopathological changes that could be correlated with changes in the biochemical profile of female albino rats. The blood plasma proteins were examined by SDS PAGE. There was no diagnostic difference in the pattern of plasma protein profile of control and treated rats. Based on the present physiological, biochemical and histological studies it is evident that imidacloprid did not produce any significant effects at 10mg/kg/day dose but induced toxicological effects at 20mg/kg/day to female rats.

Imidacloprid induced histological and biochemical alterations in liver of female albino rats.

Imidacloprid is a neonicotinoid insecticide being used extensively for crop protection and pet flea control programmes. The effect of repeated oral administration of two doses of imidcloprid (1/10th and 1/50th of LD50 of imidacloprid) on liver of female albino rat was assessed. Histological examination of liver revealed that imidacloprid (1/10th of LD50) treatment resulted in dilations of central vein and sinusoids between hepatocytes however imidacloprid (1/50th of LD50) treatment did not induce histopathological changes in liver. Non significant decrease in alkaline phosphatase (AKP) activity was observed in imidacloprid treated rats. Liver aspartate aminotransferase level showed significant increase in higher dose of imidacloprid. Additionally, significant increases in plasma levels of aspatate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (AKP) were observed in the treated rats. The results suggest that the higher doses of imidacloprid at 1/10th of LD50 is hepatotoxic as compared to lower dose of 1/50th of LD50 of imidacloprid.