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首页> 外文期刊>European journal of drug metabolism and pharmacokinetics >Mechanism of the stimulatory effect of 6-aminohexanoic acid on plasminogen activation by streptokinase or tissue plasminogen activator: the role of chloride.
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Mechanism of the stimulatory effect of 6-aminohexanoic acid on plasminogen activation by streptokinase or tissue plasminogen activator: the role of chloride.

机译:6-氨基己酸通过链激酶或组织纤溶酶原激活物对纤溶酶原激活的刺激作用机理:氯化物的作用。

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摘要

Studies were conducted on the mechanism of the stimulatory effect of 6-aminohexanoic acid (6-AH) during the in vitro activation of human glutamic plasminogen (Glu-Plg) by streptokinase or by tissue plasminogen activator (t-PA) and the possible role of the addition of physiological concentrations of NaCl to the buffer solution. Enhancement by 6-AH was investigated by measuring the rate of plasmin generation using chromogenic substrate H-D-glu-phe-lys-pNA (S-2403). Control studies using plasmin showed that the addition of 6-AH at concentrations below 20 mM did not significantly affect the initial rate of the amidolytic activity of plasmin with or without the addition of NaCl to 0.05 M Tris buffer (pH 7.4). On the other hand, addition of NaCl to the buffer slowed down the initial rate of activation of Glu-Plg by streptokinase or by t-PA while increasing the percent enhancement by 6-AH when compared with the controls. The ratios of the initial rates of plasmin generation in the presence or in the absence of 6-AH were plotted against the inverse of the volume fraction of Glu-Plg, streptokinase or t-PA after serial dilutions. The results showed that when the activation reactions were performed in 50 mM of Tris buffer (pH 7.4), the enhancements by 6-AH were related to its interaction with streptokinase or t-PA, while using the same Tris buffer containing 0.6 % NaCl, the enhancements by 6-AH were related to its interaction with both Glu-Plg and streptokinase or t-PA. However, upon increasing the NaCl to 0.9%, the results showed that the enhancements by 6-AH of the activation of Glu-Plg by streptokinase or t-PA were related to its interaction with Glu-Plg. The results suggested that changes in the concentrations of NaCl play a regulatory role during the activation process.
机译:研究了在链激酶或组织纤溶酶原激活物(t-PA)体外激活人谷氨酸纤溶酶原(Glu-Plg)时6-氨基己酸(6-AH)的刺激作用机理及其可能的作用。在缓冲溶液中添加生理浓度的氯化钠的步骤。通过使用生色底物H-D-glu-phe-lys-pNA(S-2403)测量纤溶酶的生成速率,研究了6-AH的增强作用。使用纤溶酶的对照研究表明,在20 mM以下的浓度下添加6-AH不会显着影响向或向0.05 M Tris缓冲液(pH 7.4)中添加或未添加NaCl的纤溶酶的酰胺分解活性的起始速率。另一方面,与缓冲液相比,向缓冲液中添加NaCl会减慢链激酶或t-PA活化Glu-Plg的初始速率,同时增加6-AH的百分比。将在存在或不存在6-AH的情况下纤溶酶产生的初始速率的比率与连续稀释后Glu-Plg,链激酶或t-PA的体积分数的倒数作图。结果表明,当在50 mM Tris缓冲液(pH 7.4)中进行活化反应时,6-AH的增强与其与链激酶或t-PA的相互作用有关,而使用相同的含有0.6%NaCl的Tris缓冲液, 6-AH的增强与其与Glu-Plg和链激酶或t-PA的相互作用有关。然而,当将NaCl增加至0.9%时,结果表明链激酶或t-PA通过6-AH增强Glu-Plg的活化与其与Glu-Plg的相互作用有关。结果表明,NaCl浓度的变化在激活过程中起调节作用。

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