Taurine alleviates lipopolysaccharide-induced liver injury by anti-inflammation and antioxidants in rats

被引:49
|
作者
Liu, Yueyan [1 ]
Li, Feng [1 ]
Zhang, Li [2 ]
Wu, Jianfeng [1 ]
Wang, Yanmei [2 ]
Yu, Hong [1 ]
机构
[1] West Anhui Hlth Vocat Coll, Sch Clin Med, Dept Physiol, 9 Gaocheng Rd, Luan 237005, Anhui, Peoples R China
[2] West Anhui Hlth Vocat Coll, Sch Clin Med, Dept Anat, Luan 237005, Anhui, Peoples R China
关键词
taurine; lipopolysaccharide; liver injury; NF-KAPPA-B; HEME OXYGENASE-1/CARBON MONOXIDE; COLONY-STIMULATING FACTOR; KUPFFER CELLS; OXIDATIVE MODIFICATION; HEPATIC-INJURY; ACTIVATION; ENDOTOXIN; PROTECTION; PROTEIN;
D O I
10.3892/mmr.2017.7414
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the present study was to investigate the protective effect of taurine on lipopolysaccharide (LPS)-induced liver injury and its mechanisms. Male rats were randomly divided into three groups: Normal saline, LPS model and taurine treatment. Experimental animals were treated with saline or taurine (dissolved in saline, 200 mg/kg/day) via intravenous injection. After 2 h, saline or LPS (0.5 mg/kg) was administrated via intraperitoneal injection. Markers of liver injury, pro-inflammatory cytokines and superoxide dismutase (SOD) activity were determined in plasma. Liver tissues were removed for morphological analysis and determination by western blot analysis. Taurine significantly reduced the elevation in the levels of LPS-induced aspartate transaminase and alanine transaminase and decreased the concentrations of LPS-induced inflammatory factors including tumor necrosis factor-a and interleukin-6. Taurine also increased the activity of SOD in serum and the expression of heme oxygenase-1 protein in liver tissue. Taurine pretreatment also reduced the elevated expression levels of LPS-induced cyclooxygenase-2, nuclear factor kappa B and extracellular regulated protein kinase. The results from the present study demonstrated that taurine alleviates LPS-induced liver injury. The beneficial role of taurine may be associated with its reduction of proinflamma-tory response and oxidative stress.
引用
收藏
页码:6512 / 6517
页数:6
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