de Jong F, Opthof T, Wilde A A, Janse M J, Charles R, Lamers W H, Moorman A F
Department of Anatomy and Embryology, University of Amsterdam, The Netherlands.
Circ Res. 1992 Aug;71(2):240-50. doi: 10.1161/01.res.71.2.240.
We performed a correlative electrophysiological and immunohistochemical study of embryonic chicken hearts during the septational period (Hamburger and Hamilton stages 13-31 [2-7 days of incubation]). The analyses yield conclusive evidence for slow conduction, up to 7 days of development, in the outflow tract, in the atrioventricular canal, and in the sinoatrial junction. The conduction velocity remains approximately 1 cm/sec in the outflow tract and increases in the ventricle 20-fold to approximately 20 cm/sec between 2 and 7 days of development. Transmembrane potentials of myocytes in the outflow tract and atrioventricular canal slowly rise (less than 5 V/sec), whereas in the atrium and ventricle, the upstroke velocity is eightfold to 13-fold higher. In the outflow tract, repolarization is completed only after the start of the next cycle. Because of the persistence of slow conduction, the myocardium flanking the developing atria and ventricle is thought to represent segments of persisting "primary" myocardium, whereas the more rapidly conducting "working" myocardium of the ventricle and atria is thought to represent more advanced stages of myocardial differentiation. The persisting primary myocardium was characterized by a continued coexpression of both the atrial and ventricular isoforms of myosin heavy chain. The developing atria and ventricle could be demarcated morphologically from the primary myocardium because the free walls of these segments only express their respective isoforms of myosin heavy chain. The slowly conducting myocardial zones appear to be essential for the function of the embryonic heart because 1) they provide the septating heart with alternating segments of slow and relatively fast conduction necessary for consecutive contraction of the atrial and ventricular segments and 2) their sphincterlike prolonged peristaltic contraction pattern can substitute for the adult type of one-way valves that start to develop at the end of septation.
我们对处于分隔期(汉伯格和汉密尔顿分期13 - 31期[孵化2 - 7天])的鸡胚心脏进行了相关的电生理和免疫组织化学研究。分析得出确凿证据,在发育至7天时,流出道、房室管和窦房交界处存在缓慢传导。在流出道,传导速度在发育的2至7天内保持约1厘米/秒,而在心室中增加了20倍,达到约20厘米/秒。流出道和房室管中肌细胞的跨膜电位缓慢上升(小于5伏/秒),而在心房和心室中,上升速度要高8至13倍。在流出道,复极化仅在下一个周期开始后才完成。由于缓慢传导的持续存在,围绕发育中的心房和心室的心肌被认为代表了持续存在的“原始”心肌段,而心室和心房中传导较快的“工作”心肌被认为代表了心肌分化的更高级阶段。持续存在的原始心肌的特征是肌球蛋白重链的心房和心室异构体持续共表达。发育中的心房和心室在形态上可以与原始心肌区分开来,因为这些节段的游离壁仅表达各自的肌球蛋白重链异构体。缓慢传导的心肌区域似乎对胚胎心脏的功能至关重要,因为:1)它们为正在分隔的心脏提供了心房和心室节段连续收缩所需的缓慢和相对快速传导交替的节段;2)它们类似括约肌的延长蠕动收缩模式可以替代在分隔末期开始发育的成人型单向瓣膜。