首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Guinea pig plasma kallikrein as a vascular permeability enhancement factor. Its dependence on kinin generation and regulation mechanisms in vivo.
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Guinea pig plasma kallikrein as a vascular permeability enhancement factor. Its dependence on kinin generation and regulation mechanisms in vivo.

机译:豚鼠血浆激肽释放酶是血管通透性增强因子。其对体内激肽生成和调节机制的依赖性。

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摘要

Plasma kallikrein (mol wt 80,000) was purified from guinea pig plasma, and it caused vascular permeability enhancement when injected into guinea pig skin. The activity had a linear relationship to the logarithm of kallikrein concentrations from 5 X 10(-9) M to 5 X 10(-6) M and was blocked by immunopurified anti-prekallikrein F(ab')2 rabbit antibody and soybean trypsin inhibitor. Carboxypeptidase B(1.7 units), a kinin-destructive enzyme, decreased the permeability activity to 1/20, while SQ 20,881 (10(-6) M), an inhibitor to a kinin-destructive enzyme, augmented the activity 5.4-fold. These results suggested that the permeability activity of kallikrein was performed finally through kinin generation in the skin. The permeability activity was short-lasting, and was completely blocked by a kallikrein inhibitor purified from guinea pig plasma, suggesting the presence of a down-regulation system for the permeability activity in vivo. Prostaglandin E2 (25 ng), a hyperemia inducer in microcirculation, augmented the permeability activity 12-fold, suggesting the presence of an up-regulation system in vivo. Accordingly, it was assumed that kallikrein-kinin system might play a role as a vascular permeability enhancement system in guinea pig skin.
机译:从豚鼠血浆中纯化血浆激肽释放酶(mol wt 80,000),当将其注入豚鼠皮肤时会引起血管通透性增强。活性与激肽释放酶浓度从5 X 10(-9)M到5 X 10(-6)M的对数呈线性关系,并被免疫纯化的抗早激激肽释放酶F(ab')2兔抗体和大豆胰蛋白酶抑制剂阻断。激肽破坏酶羧肽酶B(1.7个单位)将通透性活性降低至1/20,而激肽破坏酶的抑制剂SQ 20,881(10(-6)M)将活性提高了5.4倍。这些结果表明,激肽释放酶的渗透活性最终是通过皮肤中激肽的产生而进行的。通透性活性是持久的,并且被从豚鼠血浆中纯化的激肽释放酶抑制剂完全阻断,表明存在体内通透性活性的下调系统。前列腺素E2(25 ng)是微循环中的充血诱导剂,可将通透性活性提高12倍,表明体内存在上调系统。因此,据推测激肽释放酶激肽系统可能在豚鼠皮肤中起血管通透性增强系统的作用。

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