Deleted form of hepatocyte growth factor (dHGF) increases the number of platelets in rats with liver cirrhosis.

H Masunaga, N Fujise, Y Yamashita, A Shiota, H Yasuda, K Higashio
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引用次数: 4

Abstract

The effect of the deleted form of hepatocyte growth factor (dHGF) on thrombopoiesis was studied in rats. When normal rats were injected with dHGF (0.5 mg/kg i.v. twice a day), the number of platelets increased to about 1.5-fold the initial level. In addition, the treatment with dHGF (0.5 mg/kg i.v. twice daily) significantly increased the number of platelets in rats with liver cirrhosis induced by carbon tetrachloride and phenobarbital. When dHGF was given to rats at a dose of 0.05 or 0.5 mg/kg from the beginning of the induction of dimethylnitrosamine liver cirrhosis to day 28, dHGF dose-dependently ameliorated thrombocytopenia and completely prevented it at a dose of 0.5 mg/kg. These results indicate that dHGF may be applicable to the treatment of thrombocytopenia associated with liver cirrhosis.

肝细胞生长因子(dHGF)的缺失形式增加了肝硬化大鼠的血小板数量。
研究了肝细胞生长因子(dHGF)缺失形式对大鼠血小板生成的影响。正常大鼠注射dHGF (0.5 mg/kg,每天两次静脉注射)后,血小板数量增加到初始水平的1.5倍左右。此外,dHGF (0.5 mg/kg静脉滴注,每日2次)治疗可显著增加四氯化碳和苯巴比妥所致肝硬化大鼠的血小板数量。从二甲基亚硝胺性肝硬化开始到第28天,dHGF以0.05或0.5 mg/kg剂量给予大鼠,dHGF剂量依赖性地改善了血小板减少症,0.5 mg/kg剂量的dHGF完全预防了血小板减少症。这些结果表明,dHGF可能适用于治疗肝硬化伴血小板减少症。
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