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三磷酸丙吡胺和 ZD7288 对迷走神经刺激时窦房结起搏节律变化的影响。

Effects of tertiapin-Q and ZD7288 on changes in sinoatrial pacemaker rhythm during vagal stimulation.

机构信息

Department of Physiology and the Centre for Neuroscience, University of Otago, Dunedin, New Zealand.

Department of Physiology and the Centre for Neuroscience, University of Otago, Dunedin, New Zealand.

出版信息

Auton Neurosci. 2015 Dec;193:117-26. doi: 10.1016/j.autneu.2015.10.002. Epub 2015 Oct 24.

Abstract

Heart rate slowing produced by cardiac parasympathetic (vagal) stimulation is thought to be the result of modulation of the acetylcholine-activated K(+) current (IK,ACh) and the pacemaker current (If) in sinoatrial (SAN) pacemaker cells. However, the contribution of these and other ion currents to vagal slowing is controversial. Here, we examined the contributions of IK,ACh and If to vagal slowing in 15 isolated, vagal-innervated preparations of guinea-pig atria, using 300 nM tertiapin-Q (TQ) and 2 μM ZD7288 to obtain full and substantial block of these currents, respectively. Blocking IK,ACh alone reduced atrial rate responses to 10-s trains of regular vagal stimulation (supramaximal stimulation, 2-ms duration, 1-10 Hz) by ~50% (P<0.01; N=11); blocking If alone had no effect (N=7). Blocking both IK,ACh and If produced ~90% reduction (P<0.01; N=4). Atrial cycle length response to a single burst of vagal stimuli (3 stimuli at 50 Hz), delivered at the optimum phase of the cycle was strongly suppressed by blocking IK,ACh (reduced by 98%; P<0.01; N=9), and modestly reduced by blocking If alone (by ~43%; P=0.20; N=6). The response was abolished by combined block of IK,ACh and If (P=0.04; N=4). Our data show that modulation of IK,ACh and If is sufficient to account for all the vagal slowing observed in this preparation. The vagally-induced negative shift in activation potential for If will be opposed by hyperpolarisation of SAN through activation of IK,ACh. Thus removal of IK,ACh by TQ may have exaggerated the overall contribution of If to vagal slowing.

摘要

心脏迷走(副交感)神经刺激引起的心率减慢被认为是乙酰胆碱激活的 K(+)电流 (IK,ACh) 和窦房结 (SAN) 起搏细胞起搏电流 (If) 调制的结果。然而,这些和其他离子电流对迷走神经减速的贡献存在争议。在这里,我们使用 300 nM tertiapin-Q (TQ) 和 2 μM ZD7288 分别获得对这些电流的完全和实质性阻断,在 15 个分离的、迷走神经支配的豚鼠心房中检查了 IK,ACh 和 If 对迷走神经减速的贡献。单独阻断 IK,ACh 可使心房对 10 秒长的规则迷走神经刺激(超刺激,2 毫秒持续时间,1-10 Hz)的反应率降低约 50%(P<0.01;N=11);单独阻断 If 则没有影响(N=7)。同时阻断 IK,ACh 和 If 可产生约 90%的抑制作用(P<0.01;N=4)。阻断 IK,ACh 可强烈抑制对单个迷走神经刺激(50 Hz 时 3 个刺激)的心房周期长度反应(在周期的最佳相位)(减少 98%;P<0.01;N=9),单独阻断 If 则适度减少(约 43%;P=0.20;N=6)。同时阻断 IK,ACh 和 If 可使反应完全消除(P=0.04;N=4)。我们的数据表明,IK,ACh 和 If 的调制足以解释在该制剂中观察到的所有迷走神经减速。If 的激活电位的迷走神经诱导的负偏移将通过 IK,ACh 的激活使 SAN 超极化来对抗。因此,TQ 去除 IK,ACh 可能夸大了 If 对迷走神经减速的总体贡献。

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