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In vitro effect of a mucolytic thiol agent on the activity of polymorphonuclear leucocyte elastase and antileucoprotease.

机译:粘液溶解硫醇剂对多形核白细胞弹性蛋白酶和抗白蛋白蛋白酶活性的体外作用。

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摘要

We have studied the effects of the mucolytic thiol agent mercapto-ethanesulphonate (mesna) on the activity of both polymorphonuclear leucocyte (PMN) elastase and antileucoprotease in vitro. In all tests a specific synthetic substrate was used to measure elastase activity, which was then related to enzyme activity in the absence of mesna. The relative elastase activity decreased to 67.5% of control values after the enzyme had been incubated in a 120 mmol/l mesna solution. In the sol phase of purulent sputum, elastase activity decreased to 45% after the sol phase had been incubated in a 600 mmol/l mesna solution. The inability to reverse the inhibition of mesna by increasing the substrate concentration indicated that mesna acts as a non-competitive inhibitor of PMN elastase. Incubation of elastase with antileucoprotease reduced the relative elastase activity to 21%. When antileucoprotease was preincubated in a 60 mmol/l mesna solution under identical assay conditions, a relative elastase activity of 39% was observed. Inhibition experiments with mesna treated antileucoprotease, in which sulphydryl groups were blocked with iodoacetamide, strongly suggested that the dissociation constant (Ki) of the fraction of antileucoprotease that retains activity after the incubation with mesna was not changed. Elastase inhibitory activity in mucoid sol phase, which can be ascribed mainly to antileucoprotease, decreased to 53% after incubation with mesna at a concentration of 960 mmol/l. Incubation of PMN elastase/antileucoprotease complex with mesna did not result in any release of active PMN elastase from the antileucoprotease. It is concluded that mesna and other thiol compounds, when locally administered, may influence the proteinase-antiproteinase balance in the airways by their effect on both PMN elastase and antileucoprotease.
机译:我们已经研究了溶粘硫醇剂巯基乙磺酸盐(mesna)对多形核白细胞(PMN)弹性蛋白酶和抗白蛋白蛋白酶活性的影响。在所有测试中,均使用特定的合成底物来测量弹性蛋白酶的活性,然后将其与在缺少mesna的情况下的酶活性相关。在120 mmol / l甲基纤维素溶液中孵育酶后,相对弹性蛋白酶的活性降至对照值的67.5%。在化脓性痰的溶胶相中,将溶胶相在600 mmol / l二氯甲烷溶液中孵育后,弹性蛋白酶的活性降至45%。无法通过增加底物浓度来逆转对mesna的抑制,这表明mesna充当PMN弹性蛋白酶的非竞争性抑制剂。将弹性蛋白酶与抗白蛋白蛋白酶一起孵育会将相对弹性蛋白酶活性降低至21%。在相同的测定条件下,将抗白蛋白蛋白酶在60 mmol / l甲基冰钠溶液中预孵育时,观察到39%的相对弹性蛋白酶活性。 mesna处理的抗白蛋白蛋白酶的抑制实验(其中巯基被碘乙酰胺封闭)强烈表明,与mesna孵育后保留活性的抗白蛋白蛋白酶部分的解离常数(Ki)不变。在以960 mmol / l的浓度与mesna孵育后,粘液样溶胶相中的弹性蛋白酶抑制活性(主要归因于抗白细胞蛋白酶)降低至53%。将PMN弹性蛋白酶/抗白蛋白蛋白酶复合物与mesna一起孵育不会导致活性PMN弹性蛋白酶从抗白蛋白中释放出来。结论是,当局部给药时,mesna和其他硫醇化合物可能通过对PMN弹性蛋白酶和抗白蛋白蛋白酶的作用而影响气道中的蛋白酶-抗蛋白酶平衡。

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