Facebook Instagram Twitter RSS Feed PodBean Back to top on side

Protective effect of allicin against glycidamide-induced toxicity in male and female mice

In: General Physiology and Biophysics, vol. 34, no. 2
En-Ting Wang - Dong-Yan Chen - Huang-You Liu - Hai-Yang Yan - Yuan Yuan

Details:

Year, pages: 2015, 177 - 187
About article:
Acrylamide is known to be a neurotoxic, genotoxic, and carcinogenic compound. Glycidamide has a close relationship to the toxic mechanism of acrylamide. In order to explore the toxic mechanism of acrylamide, we further discussed the effects of oral administration of allicin on glycidamide-induced toxicity by determining the hematological parameters like AST, ALT, LDH, BUN, creatinine, ROS, and 8-OHdG, and biochemical parameters such as MDA, MPO, SOD, GST and GSH in the kidney, liver, brain and lung of male and female mice for the first time. We found that the same dose of glycidamide had more toxic effects and damage effects to the mice compared to the previous study of acrylamide. It could markedly increase the level of AST, ALT, LDH, BUN, ROS, 8-OHdG, MDA, MPO while decrease the SOD, GST and GSH. However, our data showed the oral administered allicin with a concentration of 5, 10, and 20 mg/kg b.w./day could significantly decrease the damage indexes of AST, ALT, LDH, BUN, ROS, 8-OHdG, MDA, and MPO, while increase the antioxidant indicators of SOD, GST and GSH. Thus allicin could be used as an effective dietary supplement for the chemoprevention of glycidamide genotoxicity internally, and to prevent the tissue damage and toxicity induced by glycidamide.
How to cite:
ISO 690:
Wang, E., Chen, D., Liu, H., Yan, H., Yuan, Y. 2015. Protective effect of allicin against glycidamide-induced toxicity in male and female mice. In General Physiology and Biophysics, vol. 34, no.2, pp. 177-187. 0231-5882.

APA:
Wang, E., Chen, D., Liu, H., Yan, H., Yuan, Y. (2015). Protective effect of allicin against glycidamide-induced toxicity in male and female mice. General Physiology and Biophysics, 34(2), 177-187. 0231-5882.