Francavilla A, Azzarone A, Carrieri G, Cillo U, Van Thiel D, Subbottin V, Starzl T E
Pittsburgh Transplant Institute, University of Pittsburgh Health Science Center, Pennsylvania 15213.
Hepatology. 1993 Mar;17(3):429-33.
Sixty-two beagle dogs were given three doses of acetaminophen over a period of 24 hr in a fulminant liver failure model that is 70% lethal in 72 hr. Treatment of the animals with hepatic stimulatory substance alone or in a mixture with insulin, transforming growth factor-alpha and insulin-like growth factor II had no effect on mortality. Evidence of maximum regeneration with a mitotic index 20 to 25 times resting was the same in treated and untreated animals. Similarly, the biochemical and hematological indexes of liver injury were unaffected by therapy. These studies illustrate the futility of treating fulminant liver failure with exogenous growth factors that apparently are already present in large amounts in the natural response to liver injury. The results suggest that on-going liver injury by mechanisms other than lack of growth factors is the central problem of fulminant liver failure. If so, provision of regeneration-stimulating substance is an inappropriate therapeutic strategy.
在一个72小时内致死率达70%的暴发性肝衰竭模型中,62只比格犬在24小时内接受了三剂对乙酰氨基酚。单独用肝刺激物质或与胰岛素、转化生长因子-α和胰岛素样生长因子II混合治疗这些动物,对死亡率没有影响。治疗组和未治疗组动物的有丝分裂指数为静息时的20至25倍,这是最大再生的证据。同样,肝损伤的生化和血液学指标也不受治疗的影响。这些研究表明,用外源性生长因子治疗暴发性肝衰竭是徒劳的,因为在肝脏损伤的自然反应中,这些生长因子显然已经大量存在。结果表明,除了缺乏生长因子之外,其他机制导致的持续性肝损伤是暴发性肝衰竭的核心问题。如果是这样,提供再生刺激物质是一种不恰当的治疗策略。