Functional role of peripheral opioid receptors in the regulation of cardiac spinal afferent nerve activity during myocardial ischemia

被引:7
作者
Fu, Liang-Wu [1 ,3 ]
Longhurst, John C. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Med, Sch Med, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Physiol & Biophys, Sch Med, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Susan Samueli Ctr Integrat Med, Sch Med, Irvine, CA 92697 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2013年 / 305卷 / 01期
关键词
sympathetic afferent nerves; opioid receptors; myocardial ischemia; naloxone; SYMPATHETIC AFFERENTS; BETA-ENDORPHIN; MOLECULAR-MECHANISMS; THROMBOXANE A(2); OPIATE RECEPTOR; GENE-EXPRESSION; MESSENGER-RNA; RAT; MU; DELTA;
D O I
10.1152/ajpheart.00091.2013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thinly myelinated A delta-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 (T-2-T-5) 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 mu mol), 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.
引用
收藏
页码:H76 / H85
页数:10
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