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World J Gastroenterol. Jan 21, 2007; 13(3): 462-466
Published online Jan 21, 2007. doi: 10.3748/wjg.v13.i3.462
Protective effect and mechanism of stronger neo-minophagen C against fulminant hepatic failure
Bao-Shan Yang, Ying-Ji Ma, Yan Wang, Li-Yan Chen, Man-Ru Bi, Bing-Zhu Yan, Lu Bai, Hui Zhou, Fu-Xiang Wang
Bao-Shan Yang, Ying-Ji Ma, Yan Wang, Li-Yan Chen, Man-Ru Bi, Bing-Zhu Yan, Lu Bai, Hui Zhou, Fu-Xiang Wang, Department of Infectious Diseases, the First Clinical Hospital of Harbin Medical University, Harbin 150001, Heilongjiang Province, China
Author contributions: All authors contributed equally to the work.
Supported by the Key Program During the Tenth Five-Year Plan of HeilongJiang Province, No. 200101031-00
Correspondence to: Yan Wang, Department of Infectious Diseases, the First Clinical Hospital of Harbin Medical University, Harbin 150001, Heilongjiang Province, China. wangyanzzz@hotmail.com
Telephone: +86-451-53601175 Fax: +86-451-53621909
Received: October 19, 2006
Revised: November 1, 2006
Accepted: November 27, 2006
Published online: January 21, 2007
Abstract

AIM: To investigate the protective effect of stronger neo-minophafen C (SNMC) on fulminant hepatic failure (FHF) and its underlying mechanism.

METHODS: A mouse model of FHF was established by intraperitoneal injection of galactosamine (D-Gal N) and lipopolysaccharide (LPS). The survival rate, liver function, inflammatory factor and liver pathological change were obtained with and without SNMC treatment. Hepatocyte survival was estimated by observing the stained mitochondria structure with terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate fluorescence nick end labeling (TUNEL) method and antibodies against cytochrome C (Cyt-C) and caspase-3.

RESULTS: The levels of plasma tumor necrosis factor alpha (TNF-α), nitric oxide (NO), ET-1, interleukin-6 (IL-6), and the degree of hepatic tissue injury were decreased in the SNMC-treated groups compared with those in the model group (P < 0.01). However, there were no differences after different dosages administered at different time points. There was a significant difference in survival rates between the SNMC-treated groups and the model group (P < 0.01). The apoptosis index was 32.3% at 6 h after a low dose of SNMC, which was considerably decreased from 32.3% ± 4.7% vs 5% ± 2.83% (P < 0.05) to 5% on d 7. The expression of Cyt-C and caspase-3 decreased with the prolongation of therapeutic time. Typical hepatocyte apoptosis was obviously ameliorated under electron microscope with the prolongation of therapeutic time.

CONCLUSION: SNMC can effectively protect liver against FHF induced by LPS/D-Gal N. SNMC can prevent hepatocyte apoptosis by inhibiting inflammatory reaction and stabilizing mitochondria membrane to suppress the release of Cyt-C and sequent activation of caspase-3.

Keywords: Stronger neo-minophagen C, Fulminant hepatic failure, Cytochrome C, Caspase-3