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Protective effects of silica hydride against carbon tetrachloride-induced hepatotoxicity in mice
Authors:Yu-Wen Hsu  Chia-Fang Tsai  Wen-Chen Chuang  Wen-Kang Chen  Yung-Chyuan Ho  Fung-Jou Lu
Institution:1. Department of Applied Chemistry, Chung Shan Medical University, No. 110, Sec. 1, Jianguo N. Rd., Taichung City 402, Taiwan;2. School of Occupational Safety and Health, Chung Shan Medical University, No. 110, Sec. 1, Jianguo N. Rd., Taichung City 402, Taiwan;3. Institute of Veterinary Pathobiology, National Chung Hsing University, No. 250, Kuo Kuang Rd., Taichung City 402, Taiwan;4. National Tainan Institute of Nursing, No. 78, Sec. 2, Minzu Rd., Tainan City, Taiwan;5. Institute of Medicine, College of Medicine, Chung Shan Medical University, No. 110, Sec. 1, Jianguo N. Rd., Taichung City 402, Taiwan;6. Department of Nutrition, Chung Shan Medical University Hospital, No. 110, Sec. 1, Jianguo N. Rd., Taichung 402, Taiwan
Abstract:The protective effects of MegaHydrate™ silica hydride against liver damage were evaluated by its attenuation of carbon tetrachloride (CCl4)-induced hepatotoxicity in mice. Male ICR mice were orally treated with silica hydride (104, 208 and 520 mg/kg) or silymarin (200 mg/kg) daily, with administration of CCl4 (1 mL/kg, 20% CCl4 in olive oil) twice a week for eight weeks. The results showed that oral administration of silica hydride significantly reduced the elevated serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), triglyceride (TG), and cholesterol and the level of malondialdehyde (MDA) in the liver that were induced by CCl4 in mice. Moreover, the silica-hydride treatment was also found to significantly increase the activities of superoxide dismutase (SOD), catalase, and glutathione peroxidase (GSH-Px), as well as increase the GSH content, in the liver. Liver histopathology also showed that silica hydride reduced the incidence of liver lesions induced by CCl4. The results suggest that silica hydride exhibits potent hepatoprotective effects on CCl4-induced liver damage in mice, likely due to both the increase of antioxidant-defense system activity and the inhibition of lipid peroxidation.
Keywords:ALP  alkaline phosphatase  ALT  alanine aminotransferase  AST  aspartate aminotransferase  CCl4  carbon tetrachloride  GSH  glutathione  GSH-Px  glutathione peroxidase  GSH-Rd  glutathione reductase  H2O2  hydrogen peroxide  MDA  malondialdehyde  ROS  reactive oxygen species  SOD  superoxide dismutase  TBA  Thiobarbituric acid  TG  triglyceride
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