Experimental Studies on Protective Effects of FK506 Against Hepatic Ischemia-Reperfusion Injury.

T. Sawada, Katsuhiko Inoue, D. Tanabe, S. Kawamoto, Tatsuya Tsuji, S. Tashiro
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引用次数: 1

Abstract

Purposes; FK506 (strong immunosuppressive agent) was investigated experimentally whether to protect the hepatic IRI. Methods; Warm ischemic experiment using pigs and rats were performed and examined whether FK506 is effective. Results; The results obtained are as follows. 1. Warm ischemia allowed time of the pigs without FK506 was 150 minutes, but as for that of FK506 group, the extension of 30 minutes was got in 180 minutes. 2. Biliary excretion rate of BSP after reperfusion were better in the group of 180 minutes ischemia with FK506 than in without FK506 group. 3. Chemiluminescence intensity in the peripheral neutrophils and adhered and infiltrated leukocytes in the liver were suppressed markedly by FK506. 4. The vascular endothelium with the scanning electron microscope was relatively preserved in the FK506 group comparing to the placebo group on 30 minutes after reperfusion. 5. Stress gastric ulcer was controlled and myeloperoxidase activity in the gastric mucosa was suppressed by FK506. Conclusion; Based on the results of theses experiments, it was suggested that FK506 has a protective effect on IRI by suppressing: the impairment of sinusoidal endothelial cells; the activation of KCs; the disturbance of micro-circulation; oxidative stress; inflammation; and the accumulation of leukocytes. J. Med. Invest. 63: 262-269, August, 2016.
FK506对肝缺血再灌注损伤保护作用的实验研究。
目的;实验研究了强免疫抑制剂FK506对肝脏IRI的保护作用。方法;用猪和大鼠进行热缺血实验,观察FK506是否有效。结果;所得结果如下:1. 无FK506组热缺血允许时间为150分钟,而FK506组在180分钟内延长了30分钟。2. FK506缺血180 min组BSP再灌注后胆汁排泄率明显高于无FK506组。3.FK506显著抑制外周中性粒细胞和肝内粘附、浸润的白细胞的化学发光强度。4. 再灌注后30分钟,FK506组与安慰剂组相比,扫描电镜下血管内皮相对保存。5. FK506可控制应激性胃溃疡,抑制胃粘膜髓过氧化物酶活性。结论;实验结果表明,FK506对IRI具有保护作用,其机制为:抑制窦状内皮细胞损伤;KCs的活化;微循环紊乱;氧化应激;炎症;白细胞的积累。[j] .中国医药科学,2016,31(3):369 - 369。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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