酪氨酸激酶抑制剂对血管平滑肌细胞中Ca2+激活的K+通道活性的调节

Zhigang Xiong, Ethan Burnette, Donald W. Cheung
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引用次数: 29

摘要

采用膜片钳记录技术研究了酪氨酸激酶抑制剂染料木素、薰衣草素A和tyrphostin A25对大鼠尾动脉单血管平滑肌细胞Ca2+活化K+通道活性的影响。染料木黄酮(5-50 μM)和薰衣草素A (10 μM)增加全细胞Ca2+激活的K+通道电流。染料木素和薰衣草素A的单通道活性也在切除后的斑块中增加。Diadzein (15 μM)是染料木黄酮的非活性类似物,不改变通道活性。Tyrphostin A25 (10 nM)在50 μM的浓度下对全细胞电流没有显著影响,但在内向外的斑块中通道的打开概率增加了841%。当从细胞内溶液中省略ATP时,染料木素未观察到全细胞和单通道活性的增强。这些观察结果表明酪氨酸激酶调节血管平滑肌细胞中Ca2+激活的K+通道活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of Ca2+-activated K+ channel activity by tyrosine kinase inhibitors in vascular smooth muscle cell

The effects of the tyrosine kinase inhibitors genistein, lavendustin A, and tyrphostin A25 on Ca2+-activated K+ channel activities in freshly isolated single vascular smooth muscle cells from the rat tail artery were studied by patch clamp recording technique. Genistein (5–50 μM) and lavendustin A (10 μM) increased whole-cell Ca2+-activated K+ channel currents. Increase in single channel activities by genistein and lavendustin A was also observed in excised inside-out patches. Diadzein (15 μM), an inactive analogue of genistein, did not alter channel activities. Tyrphostin A25 (10 nM), which had no significant effect on whole-cell currents in concentrations up to 50 μM, increased the open probability of the channels by 841% in inside-out patches. No potentiation of whole-cell and single channel activities by genistein was observed when ATP was omitted from the intracellular solutions. These observations suggest that tyrosine kinase modulates Ca2+-activated K+ channel activities in vascular smooth muscle cells.

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