Bluemel K M, Wurster R D, Randall W C, Duff M J, O'Toole M F
Department of Biology, Taylor University, Upland, Indiana 46989.
Am J Physiol. 1990 Nov;259(5 Pt 2):H1504-10. doi: 10.1152/ajpheart.1990.259.5.H1504.
Vagal ganglia that innervate the canine sinoatrial node (SAN) have been localized to a fat pad overlying and surrounding the right pulmonary vein complex (PVFP). The ventral epicardial surface of the right atrium was mapped in seven dogs anesthetized with alpha-chloralose after beta-blockade (timolol) and cardiac sympathetic and parasympathetic decentralization. A small, concentric bipolar exploring electrode was used to stimulate (during the atrial refractory period and using trains of five to eight stimuli per beat) systematically in the epicardial regions between the PVFP and the SAN. Changes in SAN rate with stimulation were measured, and the anatomic location was identified on a 150-point grid fitted to conform to size and shape of the atrium. Mapping was performed before and after local (PVFP) and systemic ganglionic blockade (hexamethonium). Data reveal that the primary vagal postganglionic pathways to the sinoatrial nodal region are subepicardial and adjacent to the SAN artery along the sulcus terminalis. Hexamethonium in the PVFP abolishes SAN inhibition during preganglionic vagal excitation, without interrupting vagal suppression of atrioventricular conduction. However, SAN slowing (with varying attenuation) continued to occur after hexamethonium (either PVFP or systemically) when the exploring electrode was applied directly over intramural postganglionic fibers between PVFP and sinus node. Attention is directed to existence of a very few synapses closer to SAN, probably in isolated ganglia immersed in fatty connective tissues along the sulcus terminalis.
支配犬窦房结(SAN)的迷走神经节已定位至覆盖并环绕右肺静脉复合体(PVFP)的脂肪垫。在用噻吗洛尔进行β受体阻滞、心脏交感神经和副交感神经去传入后,对7只经α-氯醛糖麻醉的犬的右心房腹侧心外膜表面进行标测。使用一个小型同心双极探测电极(在心房不应期且每搏施加5至8次刺激串),在PVFP和SAN之间的心外膜区域进行系统刺激。测量刺激时SAN频率的变化,并在一个适配心房大小和形状的150点网格上确定解剖位置。在局部(PVFP)和全身神经节阻滞(六甲铵)前后进行标测。数据显示,至窦房结区域的主要迷走神经节后通路位于心外膜下,沿着终沟与SAN动脉相邻。PVFP内的六甲铵可消除节前迷走神经兴奋期间的SAN抑制,而不中断迷走神经对房室传导的抑制。然而,当探测电极直接置于PVFP和窦房结之间的壁内节后纤维上方时,六甲铵(无论是PVFP局部给药还是全身给药)后SAN仍会减慢(程度不同)。值得注意的是,在更靠近SAN处存在极少数突触,可能存在于沿终沟浸于脂肪结缔组织中的孤立神经节内。