王佩, 任兴昌, 俞进, 林宜, 吴锡铭. n,n′-二乙酰-L-胱氨酸对半乳糖胺联用脂多糖引起小鼠免疫性肝衰竭的作用J. 药学学报, 2004, 39(10): 782-786.
引用本文: 王佩, 任兴昌, 俞进, 林宜, 吴锡铭. n,n′-二乙酰-L-胱氨酸对半乳糖胺联用脂多糖引起小鼠免疫性肝衰竭的作用J. 药学学报, 2004, 39(10): 782-786.
WANG Pei, REN Xing-chang, YU Jin, LIN Yi, WU Xi-ming. Influence of n,n′-diacetyl-L-cystine on D-galactosamine/lipopolysaccharide induced immunological liver failure in miceJ. Acta Pharmaceutica Sinica, 2004, 39(10): 782-786.
Citation: WANG Pei, REN Xing-chang, YU Jin, LIN Yi, WU Xi-ming. Influence of n,n′-diacetyl-L-cystine on D-galactosamine/lipopolysaccharide induced immunological liver failure in miceJ. Acta Pharmaceutica Sinica, 2004, 39(10): 782-786.

n,n′-二乙酰-L-胱氨酸对半乳糖胺联用脂多糖引起小鼠免疫性肝衰竭的作用

Influence of n,n′-diacetyl-L-cystine on D-galactosamine/lipopolysaccharide induced immunological liver failure in mice

  • 摘要: 目的研究n,n′-二乙酰-L-胱氨酸(DiNAC)对免疫性肝衰竭的治疗作用。方法观察DiNAC对Balb/C小鼠由半乳糖胺联用脂多糖引起免疫性肝衰竭的作用。半乳糖胺/脂多糖攻击6 h后,小鼠血清ALT,AST和外周血T细胞亚群分别用全自动生化仪、流式细胞仪测定,并用光镜观察肝组织病理切片,统计半乳糖胺/脂多糖攻击24 h后的小鼠存活率。结果给肝衰竭小鼠ip DiNAC(50,200,800 mg·kg-1),能明显阻止小鼠血清ALT和AST活力增高,使肝组织损害减轻及提高小鼠存活率,并呈剂量依赖关系;DiNAC能增强免疫性肝衰竭小鼠外周血CD4+,CD8+,Th1和Th2 T淋巴细胞的增殖分化。结论DiNAC对免疫性肝衰竭动物有明显的治疗作用,这一作用与其免疫调节有关。

     

    Abstract: AimTo study the therapeutic effects of n,n′-diacetyl-L-cystine (DiNAC) on immunological liver failure. MethodsSerum ALT, AST and T cell subsets in peripheral blood of the experimental animals during the trial period were analyzed by an automatic serum analyzer and a flow cytometer, respectively. The sectioned liver specimens were examined under a light microscope. And 24 h after the injection of Gal/LPS, the survival rate of rats was calculated. ResultsDiNAC (50, 200, 800 mg·kg-1, ip) suppressed the elevation of serum levels of ALT and AST, markedly enhanced proliferation and differentiation of T cell subsets (CD4+, CD8+ and Th1, Th2), and improved all the histopathological features. In mice of fulminant hepatic failure (FHF), the survival time significantly prolonged and the survival rate increased 24 h after ip DiNAC. These effects were obviously dose-dependent. Conclusion DiNAC on mice with FHF has an inhibitory action which is related to immune mechanism.

     

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