期刊
IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY
卷 38, 期 2, 页码 61-67出版社
TAYLOR & FRANCIS LTD
DOI: 10.3109/08923973.2015.1115517
关键词
Acute liver injury; anti-inflammatory; carbon tetrachloride (CCl4); heme oxygenase-1 (HO-1); resolvin D1 (RvD1)
资金
- National Natural Science Foundation of China [81072650, 81373870]
- Natural Science Foundation Project of CQ CSTC [cstc2013jcyjA10039]
Acute hepatic failure involves in excessive oxidative stress and inflammatory responses, leading to a high mortality due to lacking effective therapy. Resolvin D1 (RvD1), an endogenous lipid mediator derived from polyunsaturated fatty acids, has been shown anti-inflammatory and anti-oxidative actions, however, whether RvD1 has protective effects on hepatic failure remains elusive. In this study, the roles and molecular mechanisms of RvD1 were explored in carbon tetrachloride (CCl4)-induced acute liver injury. Our results showed that RvD1 protected mice against CCl4-induced hepatic damage, as evaluated by reduced aminotransferase activities and malondialdehyde content, elevated glutathione and superoxide dismutase activities, and alleviated hepatic pathological damage. Moreover, RvD1 significantly attenuated serum tumor necrosis factor- and interleukin-6 levels as well as hepatic myeloperoxidase activity, whereas enhanced serum IL-10 level in CCl4-administered mice. Further, RvD1 markedly up-regulated the expression and activity of heme oxygenase-1 (HO-1). However, inhibition of HO-1 activity reversed the protective effects of RvD1 on CCl4-induced liver injury. These results suggest that RvD1 could effectively prevent CCl4-induced liver injury by inhibition of oxidative stress and inflammation, and the underlying mechanism may be related to up-regulation of HO-1.
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