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依他尼酸对体外微管组装的抑制作用。

Ethacrynic acid inhibition of microtubule assembly in vitro.

作者信息

Xu S, Roychowdhury S, Gaskin F, Epstein D L

机构信息

Department of Behavioral Medicine and Psychiatry, University of Virginia School of Medicine, Charlottesville 22908.

出版信息

Arch Biochem Biophys. 1992 Aug 1;296(2):462-7. doi: 10.1016/0003-9861(92)90598-q.

Abstract

Ethacrynic acid (ECA) is a sulfhydryl reactive diuretic drug. Recent studies show that ocular administration of ECA may have potential efficacy for treatment of glaucoma. ECA affects cell shape in cultured cells from the eye outflow pathway and the microtubule system is disrupted. We have studied the effect of ECA on microtubule protein (MTP) (tubulin and microtubule-associated proteins) and purified tubulin assembly. Fifty percent inhibition of MTP (1.8 mg/ml) assembly was found at 70 microM ECA in buffer and 410 microM ECA in 30% glycerol in buffer. If all sulfhydryl groups were attributed to tubulin, then approximately two sulfhydryls were blocked at 50% inhibition. Tubulin (2 mg/ml) assembly showed 50% inhibition at 175 microM ECA and approximately 2 sulfhydryl groups were lost. Increasing ECA preincubation times (0-60 min) with tubulin showed that the longer the preincubation time, the longer the lag time, and the slower the rate of assembly and that the percentage of inhibition was proportional to the ECA preincubation time. The number of blocked sulfhydryls also increased with preincubation time. Approximately two sulfhydryls were blocked at 50% inhibition of assembly. The critical concentration for assembly increased twofold when tubulin was preincubated with 0.1 mM ECA, suggesting a loss of active tubulin. Fifty percent inhibition of taxol-induced MTP and tubulin assembly occurred at 190 and 280 microM ECA, respectively, with 3.6 to 3.8 sulfhydryls blocked, respectively. Taxol protects microtubules from disassembly by ECA, suggesting that the ECA binding key sulfhydryls are blocked in the microtubule. These results suggest that ECA reacts slowly with tubulin and blocks sulfhydryl groups important for assembly. Microtubule-associated proteins and glycerol protect the sulfhydryls and so more ECA is necessary to inhibit assembly. Since the number of blocked sulfhydryls is greater at 50% inhibition for taxol-induced microtubules, sulfhydryl blocked tubulin incompetent to assemble under normal conditions may be induced to do so with taxol.

摘要

依他尼酸(ECA)是一种具有巯基反应性的利尿药。最近的研究表明,眼部给药依他尼酸可能对青光眼治疗具有潜在疗效。依他尼酸会影响眼外流途径培养细胞的细胞形态,并且微管系统会受到破坏。我们研究了依他尼酸对微管蛋白(MTP)(微管蛋白和微管相关蛋白)以及纯化的微管蛋白组装的影响。在缓冲液中70微摩尔的依他尼酸以及在含有30%甘油的缓冲液中410微摩尔的依他尼酸时,发现微管蛋白(1.8毫克/毫升)组装受到50%的抑制。如果所有巯基都归因于微管蛋白,那么在50%抑制时大约有两个巯基被阻断。微管蛋白(2毫克/毫升)组装在175微摩尔的依他尼酸时显示出50%的抑制,并且大约有2个巯基丢失。延长依他尼酸与微管蛋白的预孵育时间(0 - 60分钟)表明,预孵育时间越长,滞后时间越长,组装速率越慢,并且抑制百分比与依他尼酸预孵育时间成正比。被阻断的巯基数量也随着预孵育时间增加。在组装受到50%抑制时大约有两个巯基被阻断。当微管蛋白与0.1毫摩尔的依他尼酸预孵育时,组装的临界浓度增加了两倍,这表明活性微管蛋白有所损失。在190和280微摩尔的依他尼酸时,紫杉醇诱导的微管蛋白和微管蛋白组装分别受到50%的抑制,分别有3.6至3.8个巯基被阻断。紫杉醇可保护微管免受依他尼酸的解聚作用,这表明依他尼酸结合的关键巯基在微管中被阻断。这些结果表明,依他尼酸与微管蛋白反应缓慢,并阻断了对组装重要的巯基。微管相关蛋白和甘油可保护巯基,因此需要更多的依他尼酸来抑制组装。由于在紫杉醇诱导的微管50%抑制时被阻断的巯基数量更多,在正常条件下无法组装的巯基被阻断的微管蛋白在紫杉醇作用下可能会被诱导进行组装。

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