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桂利嗪对补体备解素依赖性激活的抑制作用。

Inhibition by cinnarizine of the properdin-dependent activation of complement.

作者信息

Di Perri T, Auteri A, Pasini F L, Mattioli F

出版信息

Arch Int Pharmacodyn Ther. 1977 Apr;226(2):281-5.

PMID:879911
Abstract

Cinnarizine (1-benzhydryl-4-cinnamylpiperazine dihydrochloride), a well-known antagonist of vasoactive agents, has previously been shown to inhibit the activation of complement at the level of the fourth component. Cinnarizine was now tested in a system of complement activation by the properdin-dependent alternative pathway. At the concentration of 7.10(-5) M the compound completely inhibited the hemolytic reaction, which is the consequence of human complement activation in the presence of inulin or zymosan. This in vitro effect of cinnarizine was abolished by the addition of 1 mM MgCl2. These findings extend the anticomplementary activity of cinnarizine to the properdin pathway and support its interaction with the magnesium-dependent steps of the activation sequence.

摘要

桂利嗪(1-二苯甲基-4-肉桂基哌嗪二盐酸盐)是一种著名的血管活性药物拮抗剂,先前已被证明可在第四成分水平抑制补体激活。现在在由备解素依赖性替代途径介导的补体激活系统中对桂利嗪进行了测试。在7.10(-5)M的浓度下,该化合物完全抑制了溶血反应,这是在存在菊粉或酵母聚糖的情况下人补体激活的结果。加入1 mM MgCl2可消除桂利嗪的这种体外效应。这些发现将桂利嗪的抗补体活性扩展到备解素途径,并支持其与激活序列中镁依赖性步骤的相互作用。

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