Original Articles
Copyright ©The Author(s) 1999. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jun 15, 1999; 5(3): 209-212
Published online Jun 15, 1999. doi: 10.3748/wjg.v5.i3.209
Cyclosporin A protects Balb/c mice from liver damage induced by superan tigen SEB and D-GalN
Tong Yin, Shan-Qing Tong, Yu-Cai Xie, De-Yuan Lu
Tong Yin, Faculty of Medical Laboratory Sciences, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China
Shan-Qing Tong, De-Yuan Lu, Department of Microbiology, Shanghai Second Medical University, Shanghai 200025, China
Yu-Cai Xie, Department of Internal Medicine, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China
Tong Yin, female, born on 1967-07-28 in Zhenjiang City, Jiangsu Province, graduated from Shanghai Second Medical University as a postgraduate in 1996, lecturer, majoring infection and immunology, having 4 papers published.
Author contributions: All authors contributed equally to the work.
Supported by Shanghai Institute of Immunology Foundation, No.9508.
Correspondence to: Tong Yin, Faculty of Medical Laboratory Sciences, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China
Telephone: +86-21-63846590 Ext. 470
Received: January 4, 1999
Revised: February 12, 1999
Accepted: February 22, 1999
Published online: June 15, 1999
Abstract

AIM: To investigate the pathogenic effect of SEB and D-GalN on liver and the protection of cyclosporin A, the relationship between hepatic apoptosis and necrosis and the possible mechanism of acute hepatic necrosis.

METHODS: After staphylococcal enterotoxin B (SEB) mixed with D-galactosamine (D-GalN) were injected intraperitoneally into Balb/c mice and those previously treated with cyclosporin A, blood samples were collected and livers were isolated at 2, 6, 12, 24h. Patterns of hepatocellular death were studied morphologically and biochemically, circulating cytokines (TNF-α, IFN-γ) and mice mortality within 24h was assessed.

RESULTS: The SEB could induce the typical apoptotic changes of hepatocytes, the D-GalN could induce hepatocytes apoptosis and degeneration at the same time, and the mice having received the SEB + D-GalN injections developed apoptosis at 2 and 6h, but after 12h hepatocytes were characterized by severe injury, whereas all the examinations in the cyclosporin A treated mice were normal.

CONCLUSION: Hepatic cell apoptosis might be related to necrosis, and massive hepatocyte apoptosis is likely the initiating step of acute hepatic necrosis in mice. The effects induced by SEB and D-GalN on hepatocytes might be mediated by T cells, and could be prevented by cyclosporin A.

Keywords: cyclosporin A; liver necrosis; apoptosis; staphylococcal enterotoxin B; D-galactosamine