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Protective effects of oxymatrine against arsenic trioxide-induced | 48843

Journal of Neuroscience and Neuropharmacology

Protective effects of oxymatrine against arsenic trioxide-induced liver injury

4th Global Experts Meeting on Neuropharmacology

September 14-16, 2016 San Antonio, USA

Li Li

Capital Medical University, China

Posters & Accepted Abstracts: Neurochem Neuropharm

Abstract :

Oxymatrine, a quinolizidine natural drug extracted from Sophora japonica, has been reported to have neuroprotective effect and cardioprotective effect. However, the protective effect of oxymatrine on arsenic trioxide (As2O3)-induced liver injury has not been reported. In the present study, we investigated the protective effects of oxymatrine on As2O3-induced liver injury in rats. Male Wistar rats were administrated with 3 mg As2O3 intravenously on alternate days for 4 days. Oxymatrine was given 1 h before As2O3 treatment. The results showed that oxymatrine inhibited As2O3-induced hepatic pathological damage, liver ROS level and MDA level. As2O3 decreased the antioxidant enzymes SOD, GPX, and CAT activity; and the decrease was inhibited by treatment of oxymatrine. Furthermore, oxymatrine attenuated the retention of arsenic in liver tissues and improved the expression of Nrf2 and HO-1. In conclusion, our results suggested that oxymatrine protected against As2O3- induced oxidative damage by activating Nrf2/HO-1 signaling pathway.

Biography :

Li Li has completed her PhD from Peking University Health Science Center and MD from Capital Medical University in China. She has published more than 15 papers in reputed journals.

Email: lili2009kaoyan@163.com

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