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1.
Chinese Journal of Experimental and Clinical Virology ; (6): 328-331, 2004.
Article in Chinese | WPRIM | ID: wpr-279543

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression dynamics and significance of matrix metalloproteinase-2 (MMP-2) membrane type-matrix metalloproteinase-2 (MT-MMP-2) in hepatic fibrosis and its reversal counterpart.</p><p><b>METHODS</b>An experimental CCl4 induced hepatic fibrosis rat model was established by intraperitoneal administration of carbon tetrachloride for 2, 4, 6, 8, 10 weeks, and normal rats were used as a control group. The immunohistochemical methods and in situ hybridization were used to detect MMP-2,MT-MMP-2 mRNA and related antigens in the liver.</p><p><b>RESULTS</b>MMP-2,MT-MMP-2 mRNA and related antigens were expressed in mesenchymal cells and parts of hepatocytes besides active pathological changes, especially in the fibrous septum and portal area. Expression of MMP-2,MT-MMP-2 mRNA and related antigens were increased in hepatic fibrosis and decreased gradually in its reversal counterpart.</p><p><b>CONCLUSION</b>This study suggested that mesenchymal cells are the main cellular origins of MMPs. The levels of MMP-2 and MT-MMP-2 antigens and gene expression were closely related to hepatic fibrosis. MMP-2 and MT-MMP-2 may play important roles in hepatic fibrosis and its reversal counterpart.</p>


Subject(s)
Animals , Male , Rats , Carbon Tetrachloride Poisoning , Gene Expression Regulation, Enzymologic , Hepatocytes , Liver , Pathology , Liver Cirrhosis, Experimental , Pathology , Matrix Metalloproteinase 2 , Genetics , Matrix Metalloproteinases , Genetics , Matrix Metalloproteinases, Membrane-Associated , Mesenchymal Stem Cells , RNA, Messenger , Genetics , Rats, Wistar
2.
Chinese Journal of Experimental and Clinical Virology ; (6): 186-189, 2004.
Article in Chinese | WPRIM | ID: wpr-281821

ABSTRACT

<p><b>BACKGROUND</b>To investigate the effect of Oxymatrine (OM) on serum cholinesterase (ChE) during the treatment of viral hepatitis and the relationship between the change of ChE and the change of albumin (ALB), prothrombin activity (PTA) and other liver function tests.</p><p><b>METHODS</b>A total of 98 patients with viral hepatitis were divided into four groups. Group A consisted of 31 patients and were treated with OM intravenous infusion; Group B consisted of 30 patients, treated with OM orally; Group C consisted of 7 patients and were treated with OM intramuscular injection while Group D consisted of 30 patients, and were not treated with OM. ChE, ALB, PTA, liver function, renal function, soluble complement receptor-1 (sCR1) and erythrocyte innate immune adhesion function (EIIAF) were regularly determined.</p><p><b>RESULTS</b>ChE in Group A,B,C was dropped obviously during the treatment (P less than 0.001, less than 0.001, 0.023=. But there were no change in ALB, PTA, sCR1, EIIAF (P greater than 0.05), and remarkable improvement of ALT, AST, TBiL was seen during the treatment in Groups A, B, C. After the treatment with OM, the level of ChE recovered soon.</p><p><b>CONCLUSION</b>Serum level of ChE significantly declined during the treatment of viral hepatitis with OM, but no change was found in ALB, PTA, sCR1, EIIAF while liver function tests showed better results. So the drop of ChE does not mean deprivation of patient's liver disease.</p>


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Alkaloids , Therapeutic Uses , Antiviral Agents , Therapeutic Uses , Cholinesterases , Blood , Hepatitis, Viral, Human , Drug Therapy , Liver Function Tests , Quinolizines
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