Jalife J
J Physiol. 1984 Nov;356:221-43. doi: 10.1113/jphysiol.1984.sp015461.
The mechanisms of synchronous firing of cardiac pace-makers were studied using thin (0.3-0.5 mm) rabbit sino-atrial (s.a.) node strips placed in a three-compartment tissue bath. Superfusion of the central segment (1 mm in length) with ion-free sucrose solution permitted the electrical insulation of the external segments and the development of two independent pace-maker 'centres': one fast (F); one slow (S). An external shunt pathway was used to modulate the degree of coupling between F and S. Superfusion of the central segment with Tyrode solution containing heptanol (3.5 mM) instead of sucrose induced progressive decrease in the amplitude of responses in this segment and led to progressive loss of F:S synchronization. Eventually the two pace-makers became totally independent from each other. These changes were reversible upon wash-out of heptanol. When a pace-maker centre was within the range of influence of local circuit (i.e. electronic) currents from the pace-maker in the opposite side of the sucrose (or heptanol) compartment, its period was prolonged or abbreviated, depending on phase and frequency relations. Dynamic F:S interactions at various degrees of electrical coupling resulted in mutual entrainment with both pace-makers beating at simple harmonic (i.e. 1:1, 2:1, 1:2, etc.) or more complex (3:2, 5:4, etc.) ratios that depended on the degree of coupling and the intrinsic periods of the individual pace-maker centres. The patterns of synchronization could be predicted by the phasic sensitivity of each pace-maker to brief electrotonic inputs. The results suggest that when two individual pace-maker cells are connected through low resistance junctions, the period resulting from their mutual entrainment should be a function of their respective intrinsic frequencies, their phase relations and the degree of electrical coupling. The data further suggest that the heart beat is initiated by a 'democratic' type of synchronous firing of cells in the s.a. node, with each pace-maker cell contributing to an aggregate signal and involving mutual entrainment between cells.
利用置于三室组织浴中的薄(0.3 - 0.5毫米)兔窦房(s.a.)结条带,研究了心脏起搏器同步发放的机制。用无离子蔗糖溶液灌注中央节段(长度为1毫米),可使外部节段实现电绝缘,并形成两个独立的起搏器“中心”:一个快速(F);一个慢速(S)。使用外部分流途径来调节F和S之间的耦合程度。用含庚醇(3.5毫摩尔)而非蔗糖的台氏液灌注中央节段,会导致该节段反应幅度逐渐减小,并导致F:S同步性逐渐丧失。最终,两个起搏器变得完全相互独立。冲洗掉庚醇后,这些变化是可逆的。当一个起搏器中心处于蔗糖(或庚醇)隔室另一侧起搏器的局部回路(即电紧张)电流影响范围内时,其周期会延长或缩短,这取决于相位和频率关系。在不同程度的电耦合下,动态的F:S相互作用导致两个起搏器以简单谐波(即1:1、2:1、1:2等)或更复杂(3:2、5:4等)的比率相互同步跳动,这取决于耦合程度和各个起搏器中心的固有周期。同步模式可通过每个起搏器对短暂电紧张输入的相位敏感性来预测。结果表明,当两个独立的起搏器细胞通过低电阻连接时,它们相互同步产生的周期应是其各自固有频率、相位关系和电耦合程度的函数。数据进一步表明,心跳是由窦房结细胞的“民主”式同步发放引发的,每个起搏器细胞都对总信号有贡献,并涉及细胞间的相互同步。