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Potential protective effects of ginger and atorvastatin against diazinon-induced hepatotoxicity in rats: A comparative histopathological, immunohistochemical, and biochemical study

Benha Veterinary Medical Journal • 2023
العودة
معلومات البحث
المؤلفون Rania Elshafae, Ashraf Elkomy, Enas Farrag, Sabreen Ezzat Fadl, Ahmed Soliman, Mohamed Aboubakr
الكلمات المفتاحية Antioxidant; Atorvastatin; Diazinon; Ginger; Hepatotoxicity; histopathology and immunohistochemistry.
المجلة العلمية Benha Veterinary Medical Journal
الناشر Faculty of Veterinary Medicine, Benha University
المجلد 44
العدد 1
الصفحات Not Available
publication.type Local
رابط البحث Not Available
المواد المرفقة Not Available
الملخص
One of the most widely used organophosphorus insecticides for agricultural use is diazinon (DZ). In this study, we aimed to investigate the ameliorative effect of ginger (GE) and atorvastatin (ATR) against DZ-induced hepatotoxicity in rats. Seven groups of 49 males were randomly created. Group 1 (saline); group 2 (GE group; 100 mg/kg/day orally); group 3 (ATR group; 20 mg/kg/ day orally); group 4 (DZ group; 20 mg/kg/ day orally); group 5 (DZ+GE); group 6 (DZ+ATR); and group 7 (DZ+GE+ATR) for 30 days. Liver enzymes (AST, ALT, and ALP) were significantly elevated in the serum of DZ-intoxicated rats, while albumin level was dropped. Also, DZ increased cholesterol, triglycerides, LDL-C and lowered HDL-C concentrations. Additionally, a significant elevation in hepatic malondialdehyde (MDA) was recorded. Additionally, the antioxidant indicators glutathione, superoxide dismutase (SOD), and hepatic catalase (CAT) were significantly lower in the DZ-treated rats. Also, the hepatic architecture was disturbed by DZ, and the liver caspase-3 expression was considerably elevated in DZ treated group compared to control group. In DZ-intoxicated rats and co-treated with GE and ATR, there were increases in antioxidant biomarkers, decreases in MDA, and improvement in serum hepatic enzymes levels. In conclusion, GE and ATR have significant protective effects on DZ- induced hepatotoxicity via their antioxidative and antiapoptotic properties.