首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Cyclopiazonic acid an inhibitor of the sarcoplasmic reticulum Ca(2+)-pump reduces Ca(2+)-dependent K+ currents in guinea-pig smooth muscle cells.
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Cyclopiazonic acid an inhibitor of the sarcoplasmic reticulum Ca(2+)-pump reduces Ca(2+)-dependent K+ currents in guinea-pig smooth muscle cells.

机译:Cyclopiazonic酸肌浆网Ca(2+)泵的抑制剂减少豚鼠平滑肌细胞中Ca(2+)依赖的K +电流。

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摘要

1. Effects of cyclopiazonic acid (CPA), a specific inhibitor of the Ca(2+)-ATPase in sarcoplasmic reticulum (SR), on membrane ionic currents were examined in single smooth muscle cells freshly isolated from ileal longitudinal strips and urinary bladder of the guinea-pig. 2. Under whole-cell clamp, CPA (1-10 microM) reduced peak outward current elicited by depolarization in a concentration-dependent manner. The concentration of CPA required for 50% decrease in the peak outward current was approximately 3 microM in ileal cells under these conditions. The current reduced by CPA recovered by more than 70% after washout. 3. The transient outward current elicited by application of 5 mM caffeine at a holding potential of -50 mV in Ca2+ free solution was almost abolished, when the preceding Ca(2+)-loading of the cell in a solution containing 2.2 mM Ca2+ was performed in the presence of 3 microM CPA. 4. When the Ca(2+)-dependent K+ current (IK-Ca) and Ca2+ current (ICa) were inhibited by addition of Ca2+, the remaining delayed rectifier type K+ current was not affected by 10 microM CPA. When outward currents were blocked by replacement of K+ by Cs+ in the pipette solution, the remaining ICa was not affected by 10 microM CPA. 5. CPA (10 microM) did not affect the conductance of single maxi Ca(2+)-dependent K+ channels or the Cd(2+)-dependence of their open probability in both inside- and outside-out configurations. 6. These results indicate that IK-Ca is selectively and strongly suppressed by CPA.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在新鲜分离自回肠纵条和膀胱的单个平滑肌细胞中,检查了肌质网(SR)中Ca(2 +)-ATPase的一种特异抑制剂环吡嗪酸(CPA)对膜离子电流的影响。豚鼠。 2.在全细胞钳夹下,CPA(1-10 microM)以浓度依赖的方式降低了去极化引起的峰值向外电流。在这些条件下,回肠细胞中降低峰值向外电流50%所需的CPA浓度约为3 microM。冲洗后,CPA降低的电流恢复了70%以上。 3.当在含2.2 mM Ca2 +的溶液中将细胞的先前Ca(2+)负载量设为1时,几乎消除了通过在-5 mV的保持电位下以5 mM的保持电位施加5 mM咖啡因引起的瞬态向外电流。在3 microM CPA存在下执行。 4.当添加Ca2 +抑制了Ca(2+)依赖性K +电流(IK-Ca)和Ca2 +电流(ICa)时,剩余的延迟整流器类型K +电流不受10 microM CPA的影响。当通过移液器中的Cs +替代K +阻止向外电流时,剩余的ICa不受10 microM CPA的影响。 5. CPA(10 microM)不会影响单个最大的Ca(2+)依赖型K +通道的电导率,也不会影响内部和外部配置中打开概率的Cd(2+)依赖性。 6.这些结果表明,CPA对IK-Ca有选择性和强烈的抑制作用。(摘要截断为250个字)

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