Lee J H, Beitz A J
Department of Veterinary Biology, College of Veterinary Medicine, University of Minnesota, St. Paul 55108.
Brain Res. 1992 Apr 10;577(1):80-91. doi: 10.1016/0006-8993(92)90540-p.
The present study was designed to investigate the effect of 4 Hz vs. 100 Hz electroacupuncture (EA) on c-fos expression in the spinal cord induced by noxious stimulation (NS). A second objective was to evaluate the sensitivity of these two different frequencies of EA stimulation to the opiate antagonist, naloxone. Mechanical NS was applied to the right hindpaw following 30 min of either 4 Hz or 100 Hz EA treatment and the resulting c-fos expression in the spinal cord dorsal horn was compared to that obtained in rats exposed only to the noxious stimulation. The involvement of endogenous opioids in the EA response to 4 Hz or 100 Hz stimulation frequencies was evaluated by pretreating rats with naloxone (5 mg/kg, i.p.) 10 min prior to EA. Both 4 Hz and 100 Hz EA reduced the number of c-fos-immunoreactive neurons in the spinal dorsal horn induced by noxious stimulation by 58% and 50%, respectively. The suppression of c-fos expression induced by 4 Hz EA was completely reversed by prior treatment with naloxone. On the other hand, the suppression of c-fos induced by 100 Hz EA was only partially blocked by this opiate antagonist. These data indicate that both high- and low-frequency EA are capable of inhibiting the expression of c-fos in the dorsal horn induced by NS. Low-frequency EA appears to be mediated primarily by endogenous opioid systems, while non-opioid mechanisms may be involved in mediating the analgesic effect of high frequency EA. These results support the hypothesis that EA has a direct inhibitory effect on spinal cord dorsal horn neurons and extend the results of previous studies which indicate low frequency EA is mediated by opiate sensitive circuitry, while high frequency EA is predominantly mediated by non-opioid neurotransmitters.
本研究旨在探讨4Hz与100Hz电针(EA)对伤害性刺激(NS)诱导的脊髓中c-fos表达的影响。第二个目的是评估这两种不同频率的EA刺激对阿片类拮抗剂纳洛酮的敏感性。在4Hz或100Hz EA治疗30分钟后,对右后爪施加机械性NS,并将脊髓背角中由此产生的c-fos表达与仅暴露于伤害性刺激的大鼠中获得的表达进行比较。通过在EA前10分钟用纳洛酮(5mg/kg,腹腔注射)预处理大鼠,评估内源性阿片类物质在EA对4Hz或100Hz刺激频率反应中的作用。4Hz和100Hz EA分别将伤害性刺激诱导的脊髓背角中c-fos免疫反应性神经元数量减少了58%和50%。4Hz EA诱导的c-fos表达抑制被纳洛酮预处理完全逆转。另一方面,100Hz EA诱导的c-fos抑制仅被这种阿片类拮抗剂部分阻断。这些数据表明,高频和低频EA都能够抑制NS诱导的背角中c-fos的表达。低频EA似乎主要由内源性阿片类系统介导,而非阿片类机制可能参与介导高频EA的镇痛作用。这些结果支持了EA对脊髓背角神经元具有直接抑制作用的假设,并扩展了先前研究的结果,这些结果表明低频EA由阿片敏感回路介导,而高频EA主要由非阿片类神经递质介导。