Neuroscience Research Institute, Peking University, Beijing, 100191, China.
Department of Neurobiology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Neurosci Bull. 2022 Apr;38(4):403-416. doi: 10.1007/s12264-022-00844-7. Epub 2022 Apr 9.
Spinal cord stimulation (SCS)-induced analgesia was characterized, and its underlying mechanisms were examined in a spared nerve injury model of neuropathic pain in rats. The analgesic effect of SCS with moderate mechanical hypersensitivity was increased with increasing stimulation intensity between the 20% and 80% motor thresholds. Various frequencies (2, 15, 50, 100, 10000 Hz, and 2/100 Hz dense-dispersed) of SCS were similarly effective. SCS-induced analgesia was maintained without tolerance within 24 h of continuous stimulation. SCS at 2 Hz significantly increased methionine enkephalin content in the cerebrospinal fluid. The analgesic effect of 2 Hz was abolished by μ or κ opioid receptor antagonist. The effect of 100 Hz was prevented by a κ antagonist, and that of 10 kHz was blocked by any of the μ, δ, or κ receptor antagonists, suggesting that the analgesic effect of SCS at different frequencies is mediated by different endorphins and opioid receptors.
脊髓刺激 (SCS) 诱导的镇痛作用在大鼠神经病理性疼痛的 spared 神经损伤模型中得到了表征,并研究了其潜在机制。在具有中度机械性超敏反应的情况下,SCS 的镇痛作用随着刺激强度从 20%增加到 80%运动阈值而增加。各种频率(2、15、50、100、10000 Hz 和 2/100 Hz 密集分散)的 SCS 同样有效。在连续刺激 24 小时内,SCS 诱导的镇痛作用没有产生耐受。2 Hz 的 SCS 显著增加了脑脊液中的甲硫氨酸脑啡肽含量。2 Hz 的镇痛作用被 μ 或 κ 阿片受体拮抗剂所阻断。100 Hz 的作用被 κ 拮抗剂所预防,而 10 kHz 的作用则被任何 μ、δ 或 κ 受体拮抗剂所阻断,这表明不同频率的 SCS 的镇痛作用是由不同的内啡肽和阿片受体介导的。