Role of α-lipoic acid in LPS/D-GalN induced fulminant hepatic failure in mice: Studies on oxidative stress, inflammation and apoptosis

被引:70
|
作者
Xia, Xiaomin [1 ]
Su, Chuanyang [1 ]
Fu, Juanli [1 ]
Zhang, Pu [1 ]
Jiang, Xiaoji [2 ]
Xu, Demei [1 ]
Hu, Lihua [1 ]
Song, Erqun [1 ]
Song, Yang [1 ]
机构
[1] Southwest Univ, Coll Pharmaceut Sci, Key Lab Luminescence & Real Time Analyt Chem, Minist Educ, Chongqing 400715, Peoples R China
[2] 324 Hosp PLA, Dept Rehabil & Physiotherapy, Chongqing 400020, Peoples R China
基金
中国国家自然科学基金;
关键词
D-Galactosamine; Lipopolysaccharide; Hepatoprotective; Antioxidant; Inflammation; Apoptosis; NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; D-GALACTOSAMINE; SIGNALING PATHWAYS; LIPOPOLYSACCHARIDE; ACTIVATION; ANTIOXIDANT; PATHOGENESIS; INHIBITION; MECHANISMS;
D O I
10.1016/j.intimp.2014.07.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study investigated the protective effect of alpha-lipoic acid (LA) on lipopolysaccharide (LPS)/D-galactosamine (D-GalN)-induced fulminant hepatic failure in mice. First, we found that LA markedly reduced LPS/D-GalN-induced increases in serum ALT and AST activities, which were supplemented with histopathological examination, suggested that LA has a protective effect on this model of hepatic damage. Livers challenged with LPS/D-GalN exhibited extensive areas of vacuolization with the disappearance of nuclei and the loss of hepatic architecture. On the contrary, these pathological alterations were ameliorated by LA treatment. Next, we found that ROS and TBARS levels were increased in LPS/D-GalN treated liver homogenates, which were attenuated by LA administration. Consistently, decreases in hepatic CAT and GPx activities were observed in LPS/D-GalN group and were significantly restored by LA administration. Moreover, pretreatment with LA markedly reduced LPS/D-GalN-induced iNOS, COX-2, TNF-alpha, NF-kappa B, IL-1 beta and IL-6 expressions. Furthermore, our data showed that TUNEL-positive cells increased in LPS/D-GalN-treated mice liver which was counteracted by LA administration. LPS/D-GalN induced apoptosis of hepatocytes, as estimated by caspase 3, caspase 8 and caspase 9 activations. Also, the increasing of Bax and the decreasing of Bcl-2 expressions also supported LPS/D-GalN induced apoptosis. Interestingly, LA marked relieved these apoptotic features. Taking together, our results indicated that LA plays an important role on LPS/D-GalN-induced fulminant hepatic failure through its antioxidant, anti-inflammatory and antiapoptotic activities. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:293 / 302
页数:10
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