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暴露于低水平和中等水平一氧化碳的兔子体内纤维蛋白溶解的增强受到ε-氨基己酸的抑制。

Enhancement of fibrinolysis in rabbits exposed to low and moderate levels of carbon monoxide inhibited by epsilon amino caproic acid.

作者信息

Kalmaz E V, Canter L W, Coleman R L, Hampton J W

出版信息

Thromb Haemost. 1978 Feb 28;39(1):109-21.

PMID:580486
Abstract

The first (control) group of rabbits breathed ambient air whereas the second was exposed to low level carbon monoxide (CO, 50 ppm by volume) for 24 hr continuously for 8 weeks. The third group was exposed to 300 ppm CO for 4 weeks. The fourth group was exposed to 300 ppm CO for the same period of time as the third group but in addition they were also given epsilon amino caproic acid (EACA) orally, and the results compared to Group III. Per cent oxyhemoglobin (HbO2), per cent hemoglobin (Hb) and per cent carboxyhemoglobin (HbCO) were monitored in all groups. Tests of fibrinolysis were monitored and showed acceleration of the whole blood clot lysis and euglobulin lysis times (ELT). A fibrin plate test confirmed the increased lysis and serum fibrin and/or fibrinogen degradation products (FDP) were elevated in the CO exposed animals. No changes were observed in the same tests in the rabbits exposed to ambient air. The fourth group of animals receiving EACA showed inhibition of lysis and decrease in serum FDP. Alpha-1-antitrypsin and alpha-2-macroglobulin assays in all groups showed no change. Microscopic examination of the large vessels in these test groups showed endothelial damage which indicates a possible source for a plasminogen activator release, or lead to action of Hageman factor and activated plasma plasminogen proactivator.

摘要

第一组(对照组)兔子呼吸环境空气,而第二组兔子连续8周每天24小时暴露于低水平一氧化碳(CO,体积分数为50 ppm)环境中。第三组兔子暴露于300 ppm CO环境中4周。第四组兔子与第三组暴露于300 ppm CO环境中的时间相同,但除此之外还口服ε-氨基己酸(EACA),并将结果与第三组进行比较。监测所有组的氧合血红蛋白(HbO2)百分比、血红蛋白(Hb)百分比和碳氧血红蛋白(HbCO)百分比。监测纤维蛋白溶解试验,结果显示全血凝块溶解和优球蛋白溶解时间(ELT)加快。纤维蛋白平板试验证实暴露于CO环境中的动物的溶解增加,血清纤维蛋白和/或纤维蛋白原降解产物(FDP)升高。在呼吸环境空气的兔子的相同试验中未观察到变化。接受EACA的第四组动物显示溶解受到抑制,血清FDP降低。所有组的α-1-抗胰蛋白酶和α-2-巨球蛋白检测均未显示变化。对这些试验组的大血管进行显微镜检查显示存在内皮损伤,这表明可能是纤溶酶原激活物释放的来源,或导致了Hageman因子和活化血浆纤溶酶原激活剂的作用。

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