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抗凝血酶III和肝素在凝血酶相关反应中的失活作用。

Antithrombin III and heparin inactivation in thrombin involving reactions.

作者信息

Marciniak E

出版信息

Thromb Haemost. 1977 Aug 31;38(2):486-93.

PMID:579490
Abstract

The inhibitory capacity of antithrombin III (AT III) was measured by a quantitative method independent of the velocity of inhibition. When AT III was in excess of thrombin in plasma or in purified system the capacity of inhibitor decreased quantitatively in proportion to the amount of thrombin neutralized. Heparin present in reaction together with thrombin invariably induced a more extensive utilization of inhibitor than thrombin alone. The extent of this additional loss of inhibitory capacity was to a limited degree related to the concentration of heparin. Heparin itself was neutralized in thrombin-AT III reaction losing its anticoagulant property in proportion to the amount of thrombin bound by inhibitor. This quantitative neutralization of heparin occurred not only when the anticoagulant participated in thrombin-AT III binding but also when heparin was added to a medium containing a preformed thrombin-AT III complex. These results suggest that acceleration of binding and increased utilization of binding capacity are the two regular effects of heparin on thrombin-involving reactions of AT III. Both of these effects may be abolished by quantitative binding of heparin to thrombin-AT III complex.

摘要

抗凝血酶III(AT III)的抑制能力通过一种与抑制速度无关的定量方法进行测定。当血浆或纯化系统中AT III过量于凝血酶时,抑制剂的能力会随着被中和的凝血酶量成比例地定量下降。与凝血酶一起存在于反应中的肝素总是比单独的凝血酶诱导更广泛地利用抑制剂。这种抑制能力额外损失的程度在一定程度上与肝素的浓度有关。肝素本身在凝血酶-AT III反应中被中和,其抗凝特性会随着被抑制剂结合的凝血酶量成比例地丧失。肝素的这种定量中和不仅发生在抗凝剂参与凝血酶-AT III结合时,也发生在将肝素添加到含有预先形成的凝血酶-AT III复合物的介质中时。这些结果表明,加速结合和增加结合能力的利用是肝素对涉及AT III的凝血酶反应的两个常规效应。通过肝素与凝血酶-AT III复合物的定量结合,这两种效应都可能被消除。

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