Protective effect of Acanthopanax gracilistylus-extracted Acankoreanogenin A on mice with fulminant hepatitis

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• 作者：Bao-Xin Zhang^a ; ^{zhangbx73@126.com"" rel=""nofollow} ; Ning Li^b ; ^{nxli1970@126.com"" rel=""nofollow} ; Zu-Ping Zhang^c ; ^{zhangzp74@126.com"" rel=""nofollow} ; Hong-Bo Liu^a ; ^{lhpop@126.com"" rel=""nofollow} ; Rong-Rong Zhou^a ; ^{rr-xy@hotmail.com"" rel=""nofollow} ; Bai-Yun Zhong^d ; ^{zhongby6@tom.com"" rel=""nofollow} ; Ming-Xiang Zou^d ; ^{zoumingxiang@126.com"" rel=""nofollow} ; Xia-Hong Dai^a ; ^{daixiahong.student@sina.com"" rel=""nofollow} ; Mei-Fang Xiao^a ; ^{xmf427@126.com"" rel=""nofollow} ; Xiang-Qian Liu^e ; ^{lxq123@163.com"" rel=""nofollow} ; Xue-Gong Fan^a ; ^{xgfan@hotmail.com"" rel=""nofollow} ; ^{xgfan57@126.com"" rel=""nofollow}
• 关键词：Acankoreanogenin A ; Fulminant hepatitis ; Inflammatory cytokine ; HMGB1
• 刊名：International Immunopharmacology
• 出版年：2011
• 出版时间：August 2011
• 年：2011
• 卷：11
• 期：8
• 页码：1018-1023
• 全文大小：1007 K

文摘

The release of pro-inflammatory cytokines in both acute (IL-1β and TNF-α) and chronic [high mobility group box 1 protein (HMGB1)] phases, is thought to play important roles in the development of fulminant hepatitis (FH). Triterpenoid Acankoreanogenin A (AA) which is extracted from the leaves of the Acanthopanax gracilistylus W.W. Smith (AGS) has shown its inhibiting effect on TNF-α, IL-1β and HMGB1 release in vitro in our preliminary experiments. In present study, we investigated the effect of AA on mice with fulminant hepatitis in vivo. Fulminant hepatitis mice model was established by intraperitoneally injecting galactosamine (GalN) and lipopolysaccharide (LPS). The levels of serum of TNF-α, IL-1β, ALT, AST and HMGB1 from AA-treated mice were measured at different time points. Our results demonstrated that pre-treatment of mice with AA markedly reduced the serum levels of TNF-α, IL-1β, HMGB1, ALT and AST with the improvement in histological features. And the survival rate from AA-treated fulminant hepatitis mice was increased. Furthermore, delayed administration of AA after peak occurrence of the early pro-inflammatory cytokines still endowed significant protection against GalN/LPS-induced lethality. The post-treatment of AA could significantly attenuate the release of HMGB1, but not the TNF-α and IL-1β. These results indicate that AA inhibits the systemic release of pro-inflammatory cytokine HMGB1, and dose-dependently rescue the mice from lethal GalN/LPS-induced fulminant hepatitis, which suggests this component as a candidate therapy for fulminant hepatitis.