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急性期反应物会加重大鼠四氯化碳诱导的肝硬化。

Acute phase reactants enhance CCl4 induced liver cirrhosis in the rat.

作者信息

van Gool J, van Vugt H, de Nie I

出版信息

Exp Mol Pathol. 1986 Apr;44(2):157-68. doi: 10.1016/0014-4800(86)90066-3.

Abstract

High levels of acute phase proteins (acute phase reactants, APR) suppress acute inflammatory reactions in the rat. As many APR have antiprotease properties, including an anticollagenase activity, the effect of APR on the development of CCl4-induced liver fibrosis was investigated in rats. APR were provoked by repeated injections of epinephrine, inducing a broad spectrum of APR. This reaction can be monitored measuring alpha 2-macroglobulin levels in the rat (alpha 2-macrofetoprotein, alpha M FP). This protein was found to inhibit both acute galactosamine hepatitis and acute CCl4-induced liver toxicity. The animals with high levels of APR at the start of CCl4 treatment developed a more severe degree of fibrosis and cirrhosis than the control group in which no acute phase reaction was induced. Epinephrine alone had no such effects. Additionally, the APR positive group showed an initially lower degree of hepatocellular damage when compared to control animals. This uncoupling of liver cell damage and subsequent fibrosis may demonstrate that higher levels of APR might be important as to the development of cirrhosis, possibly based on the anticollagenase activity of these proteins.

摘要

高水平的急性期蛋白(急性期反应物,APR)可抑制大鼠的急性炎症反应。由于许多APR具有抗蛋白酶特性,包括抗胶原酶活性,因此研究了APR对大鼠四氯化碳诱导的肝纤维化发展的影响。通过反复注射肾上腺素激发APR,诱导产生多种APR。这种反应可通过测量大鼠体内α2-巨球蛋白水平(α2-甲胎蛋白,αM FP)来监测。发现这种蛋白可抑制急性半乳糖胺肝炎和急性四氯化碳诱导的肝毒性。在四氯化碳治疗开始时APR水平高的动物,与未诱导急性期反应的对照组相比,发生了更严重程度的纤维化和肝硬化。单独使用肾上腺素没有这种作用。此外,与对照动物相比,APR阳性组最初肝细胞损伤程度较低。肝细胞损伤与随后纤维化的这种脱节可能表明,较高水平的APR对于肝硬化的发展可能很重要,这可能基于这些蛋白的抗胶原酶活性。

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