Vitamin E and selenium treatment of monocrotaline induced hepatotoxicity in rats

Abstract

Monocrotaline (MCT) is a hepatotoxic pyrrolizidine alkaloid that is derived from plants; exposure may occur by consumption of contaminated grains, herbal teas and medicines. MCT can cause liver damage. We investigated the antioxidant effects of selenium (Se) and vitamin E against the toxic effects of MCT. Female Wistar albino rats were divided into four groups: a control group, an MCT group, an MCT + Se group, and an MCT + vitamin E group. Liver tissues were harvested, fixed, processed to paraffin and sections were cut. Anti-von Willebrand factor (vWF) immunohistochemistry, terminal deoxynucleotidyl transferase dUTP nick end-labeling (TUNEL), and hematoxylin and eosin staining were performed. Serum and liver tissue glutathione (GSH), catalase (CAT), and glutathione peroxidase (GPx) levels were measured. Histopathological and TUNEL data showed significantly increased liver damage in the MCT group compared to controls. Histopathological and TUNEL staining indicated significant improvements in the MCT + vitamin E and MCT + Se groups compared to the MCT group. MCT significantly reduced the serum GSH level and GPx activity, and liver GPx activity. Biochemical data indicated a significant improvement in serum GSH level in the MCT + vitamin E group compared to the MCT group. We suggest that vitamin E and Se afford limited protection against MCT hepatotoxicity.

Key words:

• catalase
• glutathione
• glutathione peroxidase
• histopathology
• liver
• TUNEL
• GPx
• monocrotalin
• rats
• selenium
• vitamin E
• von Willebrand factor

Acknowledgment

Our research was supported by a grant from the Scientific Research Projects Coordination Office of Necmettin Erbakan University, Konya, Turkey, Project No. 151218012.

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this paper.