Salata J J, Jalife J
Circ Res. 1985 May;56(5):718-27. doi: 10.1161/01.res.56.5.718.
Previous studies have suggested that maintained vagal stimulation or acetylcholine infusion results in a fade of responses in the sinoatrial node but not in the atrioventricular node, implying different muscarinic receptor subtypes in the two regions. We investigated this hypothesis in 23 isolated rabbit atrial preparations made quiescent by continuous superfusion with verapamil (1 microgram/ml). Transmembrane potentials were recorded simultaneously from cells in the sinoatrial pacemaker region and from the "N" region of the atrioventricular node. Postganglionic vagal stimulation was achieved by the application of trains of pulses (50-150 microseconds; 10-20 V; 200 Hz). Simultaneous application of long-lasting (1-10 sec) vagal trains produced hyperpolarizations which were nearly identical for both nodal regions. Maximal hyperpolarizations (approximately or equal to 24 mV for sinoatrial node; 26 mV for atrioventricular node) were reached about 500 msec after initiation of the vagal train. Thereafter, hyperpolarizations faded, following a biphasic time course, and thus displaying two different time constants, one fast (tau fast = 580 msec for sinoatrial node; 550 msec for atrioventricular node), and one slow (tau slow = 9.2 sec for both sinoatrial and atrioventricular nodes). Hyperpolarizations during brief (200-msec) but repetitive vagal trains also faded biphasically, but approached a steady state much more rapidly than responses to long-lasting trains. Recovery from hyperpolarization decay occurred rather slowly and was linear. Our results demonstrate that the membrane potential responses to vagal stimulation in the atrioventricular node are indistinguishable from those in the sinoatrial node, and suggest that similar muscarinic receptors are operative in both regions. These phenomena may play an important role in the response of the cardiac conducting system to direct or reflexly mediated vagal input.
以往的研究表明,持续的迷走神经刺激或乙酰胆碱注入会导致窦房结的反应逐渐减弱,但房室结却不会,这意味着两个区域存在不同的毒蕈碱受体亚型。我们在23个通过用维拉帕米(1微克/毫升)持续灌流使其静止的离体兔心房标本中研究了这一假设。同时记录窦房结起搏区域细胞和房室结“N”区域细胞的跨膜电位。通过施加脉冲串(50 - 150微秒;10 - 20伏;200赫兹)实现节后迷走神经刺激。同时施加持续时间长(1 - 10秒)的迷走神经脉冲串会产生超极化,两个结区的超极化几乎相同。迷走神经脉冲串开始后约500毫秒达到最大超极化(窦房结约为或等于24毫伏;房室结为26毫伏)。此后,超极化呈双相时间进程逐渐减弱,因此显示出两个不同的时间常数,一个快(窦房结的τ快 = 580毫秒;房室结的τ快 = 550毫秒),一个慢(窦房结和房室结的τ慢均为9.2秒)。短暂(200毫秒)但重复的迷走神经脉冲串期间的超极化也呈双相减弱,但比持续时间长的脉冲串反应更快地接近稳态。超极化衰减后的恢复相当缓慢且呈线性。我们的结果表明,房室结对迷走神经刺激的膜电位反应与窦房结的反应没有区别,并表明两个区域都有类似的毒蕈碱受体起作用。这些现象可能在心脏传导系统对直接或反射介导的迷走神经输入的反应中起重要作用。