首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Blocking action of chromanol 293B on the slow component of delayed rectifier K+ current in guinea-pig sino-atrial node cells
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Blocking action of chromanol 293B on the slow component of delayed rectifier K+ current in guinea-pig sino-atrial node cells

机译:色酚293B对豚鼠鼻窦房结细胞中延迟整流K +电流慢成分的阻断作用

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摘要

class="enumerated" style="list-style-type:decimal">In guinea-pig sino-atrial (SA) node cells the delayed rectifier K+ current (IK) is composed of rapidly and slowly activating components of IK (IKr and IKs, respectively). The present study was undertaken to characterize the blocking action of the chromanol derivative 293B on IKs in guinea-pig SA node cells using whole-cell patch-clamp technique.Bath application of 293B blocked IKs, elicited by 4-s depolarizing voltage pulses from a holding potential of −50 mV, under conditions in which the L-type Ca2+ current (ICa,L) and IKr were inhibited; the effect was concentration-dependent with an IC50 of 5.3 μM, when evaluated by the decrease in the amplitude of IKs tail current following 4-s depolarizing voltage steps to +50 mV.The 293B block of IKs progressed with time during depolarizing voltage steps with a more rapid block at higher concentrations.The block of IKs by 293B was fully reversed within a few minutes after washing off the drug, even when a maximal effect (a nearly full block) was achieved at high drug concentration (50 μM).Bath application of 293B at 50 μM greatly and reversibly reduced the amplitude of IKs which is maximally stimulated by β-adrenergic agonist isoprenaline (1 μM), while the degree of 293B block of the isoprenaline-stimulated IKs was slightly but significantly smaller than that of non-stimulated IKs (94.0±0.98% block, n=6 vs 99.4±0.45% block, n=6; P<0.01).We conclude that, in guinea-pig SA node cells (i) 293B is a potent and fully reversible blocker of IKs in control and during β-adrenergic stimulation and (ii) block with 293B occurs in a time-dependent manner during depolarizing voltage steps.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在几内亚猪的心房(SA)节点细胞中,延迟整流器K + 电流(IK)由IK的快速激活成分和缓慢激活的成分(分别为IKr和IKs)组成。本研究利用全细胞膜片钳技术表征了苯并二氢吡喃酚衍生物293B对豚鼠SA节点细胞IKs的阻断作用。 293B阻断IKs在浴中的应用4 -s在保持L型Ca 2 + 电流(ICa,L)和IKr的条件下从保持电位为-50 mV的去极化电压脉冲;通过以4s的去极化电压步进至+50 mV后IKs尾电流的幅度减小来评估,该效应与浓度有关,IC50为5.3μM。 IK的293B阻滞进展随着时间的流逝,在较高的浓度下会更快地阻断极化。 洗出药物后的几分钟内,293B的IKs阻断被完全逆转,即使效果最大(接近完全) 在50μM的浴液中应用293B极大地并且可逆地降低了IKs的振幅,IK的振幅最大程度地受到了β-肾上腺素能激动剂异丙肾上腺素(1μM)的刺激,异丙肾上腺素刺激的IKs的293B阻滞程度比未刺激的IKs稍高但显着较小(94.0±0.98%阻滞,n = 6 vs 99.4±0.45%阻滞,n = 6; P < /em><0.01)。 我们得出的结论是,在豚鼠SA结细胞中,(i)293B是 I Ks在β肾上腺素能刺激中以及在(ii)293B阻滞在去极化电压阶跃过程中以时间依赖的方式发生。

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