Minisi A J, Thames M D
Department of Medicine, Medical College of Virginia/Virginia Commonwealth University, Richmond.
Circulation. 1991 Jul;84(1):357-67. doi: 10.1161/01.cir.84.1.357.
Left ventricular sympathetic afferent nerves are located mainly in superficial epicardial layers. Reflex excitatory responses mediated by sympathetic afferent nerves have been observed during myocardial ischemia in cats and humans but not in dogs. Previous canine studies have induced ischemia by occlusion of a coronary artery. Extensive collateral circulation in the canine heart may limit ischemia of epicardial layers during simple coronary occlusion, resulting in little stimulation of sympathetic afferent nerves and minimal reflex excitatory responses.
In anesthetized dogs with sinoaortic and vagal deafferentation, we determined whether reflex sympathoexcitatory responses mediated by sympathetic afferents occurred during transmural myocardial ischemia. Reflex sympathoexcitation was quantitated by direct recording from either efferent renal (n = 20) or cardiac (n = 5) sympathetic nerves. Responses of arterial pressure and efferent sympathetic nerve activity were measured during simple occlusion of the anterior descending artery (LAD alone) and during LAD occlusion with a circumflex stenosis (LAD + CIRC). This circumflex stenosis was adjusted to abolish coronary vasodilator reserve without reducing basal flow. We observed significantly greater reflex increases in renal (32 +/- 5%) and cardiac (58 +/- 15%) nerve activity during LAD + CIRC than during LAD alone (14 +/- 6% and 8 +/- 7%, respectively). Reflex changes in renal nerve activity during LAD + CIRC were abolished by interruption of cardiac sympathetic afferent pathways (n = 5). In eight experiments, myocardial blood flow was measured during the two coronary occlusions. These experiments confirmed that LAD + CIRC elicited more transmural ischemia in the LAD distribution than did LAD alone. However, these experiments also revealed that LAD + CIRC elicited endocardial ischemia in the circumflex distribution. In five additional experiments, regional sympathetic deafferentation of the posterior left ventricle by epicardial application of 88% phenol along the atrioventricular groove had no significant effect on renal nerve responses to LAD + CIRC (36 +/- 5% increase before phenol versus 31 +/- 3% increase after phenol). These results indicate that endocardial ischemia in the circumflex distribution did not contribute to the reflex increases in nerve activity that were noted during LAD + CIRC.
Reflex sympathoexcitation mediated by cardiac sympathetic afferents can be elicited in dogs. However, these responses are significant only during ischemia that is transmural and involves the superficial epicardial layers of the left ventricle.
左心室交感传入神经主要位于心外膜浅层。在猫和人类的心肌缺血过程中已观察到由交感传入神经介导的反射性兴奋反应,但在犬类中未观察到。以往的犬类研究通过冠状动脉闭塞诱导缺血。犬类心脏广泛的侧支循环可能会限制单纯冠状动脉闭塞期间心外膜层的缺血,导致交感传入神经刺激很少,反射性兴奋反应最小。
在去窦主动脉和迷走神经传入的麻醉犬中,我们确定在透壁心肌缺血期间是否发生由交感传入神经介导的反射性交感神经兴奋反应。通过直接记录传出肾交感神经(n = 20)或心脏交感神经(n = 5)来定量反射性交感神经兴奋。在单纯闭塞前降支动脉(仅LAD)以及前降支动脉闭塞合并回旋支狭窄(LAD + CIRC)期间测量动脉血压和传出交感神经活动的反应。调整该回旋支狭窄以消除冠状动脉扩张储备而不降低基础血流。我们观察到,与仅LAD闭塞期间(分别为14±6%和8±7%)相比,LAD + CIRC期间肾神经活动(32±5%)和心脏神经活动(58±15%)的反射性增加明显更大。LAD + CIRC期间肾神经活动的反射性变化在心脏交感传入通路中断后消失(n = 5)。在8个实验中,在两种冠状动脉闭塞期间测量心肌血流量。这些实验证实,与仅LAD闭塞相比,LAD + CIRC在LAD分布区域引起更多的透壁缺血。然而,这些实验还表明,LAD + CIRC在回旋支分布区域引起心内膜缺血。在另外5个实验中,沿房室沟心外膜应用88%苯酚对左心室后壁进行局部交感神经去传入对肾神经对LAD + CIRC的反应没有显著影响(苯酚应用前增加36±5%,应用后增加31±3%)。这些结果表明,回旋支分布区域的心内膜缺血对LAD + CIRC期间观察到的神经活动反射性增加没有贡献。
在犬类中可引发由心脏交感传入神经介导的反射性交感神经兴奋。然而,这些反应仅在透壁且涉及左心室心外膜浅层的缺血期间才显著。