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  • Title: Suppression of cytokine production by thromboxane A2 inhibitor in liver ischemia.
    Author: Sugawara Y, Harihara Y, Takayama T, Makuuchi M.
    Journal: Hepatogastroenterology; 1998; 45(23):1781-6. PubMed ID: 9840148.
    Abstract:
    BACKGROUND/AIMS: The possible involvement of a thromboxane (TX) A2 inhibitor, sodium ogzarel (SO) was investigated in the regulation of tumor necrosis factor (TNF) alpha and interleukin (IL)1-alpha in liver ischemia and reperfusion (I/R) injury. METHODOLOGY: Rat livers were subjected to 90 min of total hepatic ischemia. Five minutes before the ischemia insult, 10 mg/kg of SO was administered intravenously (SO group); control animals received normal saline solution (NS group). Plasma levels of aspartate aminotransferase (AST), hyaluronic acid (HA), TNF-alpha, IL-1 alpha and three plastanoids, 6-keto prostaglandin (PG) F1 alpha, PGE2 and TXB2, were measured before ischemia insult and 5, 60 and 120 min after reperfusion. Parts of the left lateral lobe were taken for measurement of adenosine nucleotides and histological examination. The cumulative survival rates for the first 10 days after I/R injury were examined for each group. SO was administered at various doses (0.3-30 mg/kg) and TXB2, TNF-alpha and IL-1 alpha were measured. RESULTS: Significant differences were recognized between the plasma AST, HA, TXB2, TNF-alpha, IL-1 alpha and energy charge levels, the degree of liver necrosis and survival rates of the two groups. Dose-dependent inhibition by SO of the production of TXB2, TNF-alpha and IL-1 alpha was observed. CONCLUSIONS: Regulation of TNF-alpha and IL-1 alpha by SO is possibly associated with the hepatoprotective effect of SO.
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