Department of Medicine, School of Medicine, University of California, Irvine, CA 92697, USA.
Am J Physiol Heart Circ Physiol. 2013 Jul 1;305(1):H76-85. doi: 10.1152/ajpheart.00091.2013. Epub 2013 May 3.
Thinly myelinated Aδ-fiber and unmyelinated C-fiber cardiac sympathetic (spinal) sensory nerve fibers are activated during myocardial ischemia to transmit the sensation of angina pectoris. Although recent observations showed that myocardial ischemia increases the concentrations of opioid peptides and that the stimulation of peripheral opioid receptors inhibits chemically induced visceral and somatic nociception, the role of opioids in cardiac spinal afferent signaling during myocardial ischemia has not been studied. The present study tested the hypothesis that peripheral opioid receptors modulate cardiac spinal afferent nerve activity during myocardial ischemia by suppressing the responses of cardiac afferent nerve to ischemic mediators like bradykinin and extracellular ATP. The nerve activity of single unit cardiac afferents was recorded from the left sympathetic chain (T₂-T₅) in anesthetized cats. Forty-three ischemically sensitive afferent nerves (conduction velocity: 0.32-3.90 m/s) with receptive fields in the left and right ventricles were identified. The responses of these afferent nerves to repeat ischemia or ischemic mediators were further studied in the following protocols. First, epicardial administration of naloxone (8 μmol), a nonselective opioid receptor antagonist, enhanced the responses of eight cardiac afferent nerves to recurrent myocardial ischemia by 62%, whereas epicardial application of vehicle (PBS) did not alter the responses of seven other cardiac afferent nerves to ischemia. Second, naloxone applied to the epicardial surface facilitated the responses of seven cardiac afferent nerves to epicardial ATP by 76%. Third, administration of naloxone enhanced the responses of seven other afferent nerves to bradykinin by 85%. In contrast, in the absence of naloxone, cardiac afferent nerves consistently responded to repeated application of ATP (n = 7) or bradykinin (n = 7). These data suggest that peripheral opioid peptides suppress the responses of cardiac sympathetic afferent nerves to myocardial ischemia and ischemic mediators like ATP and bradykinin.
薄髓 Aδ 纤维和无髓 C 纤维心脏交感(脊髓)感觉神经纤维在心肌缺血时被激活,以传递心绞痛的感觉。尽管最近的观察表明,心肌缺血会增加阿片肽的浓度,并且外周阿片受体的刺激会抑制化学诱导的内脏和躯体痛觉,但阿片类物质在心肌缺血期间心脏脊髓传入信号中的作用尚未得到研究。本研究假设外周阿片受体通过抑制心脏传入神经对缓激肽和细胞外 ATP 等缺血介质的反应来调节心肌缺血期间心脏脊髓传入神经活动。在麻醉猫的左侧交感神经链(T₂-T₅)上记录单个单位心脏传入神经的神经活动。鉴定出 43 根对缺血敏感的传入神经(传导速度:0.32-3.90 m/s),其感受野位于左心室和右心室。在以下方案中,进一步研究了这些传入神经对重复缺血或缺血介质的反应。首先,心脏表面给予纳洛酮(8 μmol),一种非选择性阿片受体拮抗剂,使 8 根心脏传入神经对反复心肌缺血的反应增强了 62%,而心脏表面给予载体(PBS)并未改变另外 7 根心脏传入神经对缺血的反应。其次,纳洛酮应用于心外膜表面使 7 根心脏传入神经对心外膜 ATP 的反应增加了 76%。第三,给予纳洛酮使另外 7 根传入神经对缓激肽的反应增强了 85%。相比之下,在没有纳洛酮的情况下,心脏传入神经始终对反复应用 ATP(n = 7)或缓激肽(n = 7)有反应。这些数据表明,外周阿片肽抑制心脏交感传入神经对心肌缺血和 ATP 及缓激肽等缺血介质的反应。