| Autor: |
Noguchi, Toshinori, Matsuyama, Shyutoku, Akao, Makoto, Hagiwara, Hiromi, Uno, Shigeyuki, Seki, Taiichiro, Ariga, Toyohiko |
| Zdroj: |
Thrombosis Research; November 2001, Vol. 104 Issue: 4 p283-291, 9p |
| Abstrakt: |
Background/Aims:The plasminogen activator (PA)–plasmin system is primarily involved in fibrinolysis, but is also in the patho/physiological events in which breakdown of extracellular matrices is evoked topically. In this present study, we examined the expression of fibrinolytic factors, tissue-type PA (t-PA) and Type 1 PA inhibitor (PAI-1), in acute liver injury. Methods:Acute liver injury was produced in rats by the intraperitoneal administration of carbon tetrachloride (CCl4). Plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities were measured to verify the hepatocellular damage. t-PA and PAI-1 gene expressions were measured by Northern blotting, and the cell type(s) expressing these genes was identified by in situ hybridization. t-PA and PAI-1 levels were measured by enzyme-linked immunosorbent assay (ELISA). Results:A single intraperitoneal administration of CCl4caused severe acute parenchymatous liver injury. Both t-PA and PAI-1 gene expressions were induced by the acute liver injury, and plasma t-PA and PAI-1 concentrations were also increased. In situ hybridization studies demonstrated that the hepatocytes were the cells expressing t-PA and PAI-1 genes during the acute liver injury. t-PA was also augmented in the bile, whereas PAI-1 was decreased there. Conclusions:t-PA and PAI-1 gene expressions are induced in the hepatocytes of rats with acute liver injury. These fibrinolytic factors induced by liver injury may play important roles in liver regeneration. |
| Databáze: |
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