High intensity magnetic stimulation over the lumbosacral spine evokes antinociception in rats

被引:11
作者
Lin, VWH
Hsiao, I
Kingery, WS
机构
[1] VA Long Beach Hlth Care Syst, Spinal Cord Injury Disorder Hlth Care Grp, Functional Magnet Stimulat Lab, Long Beach, CA 90822 USA
[2] Univ Calif Irvine, Dept Phys Med & Rehabil, Irvine, CA USA
[3] Stanford Univ, Sch Med, Dept Functional Restorat, Stanford, CA USA
[4] Vet Affairs Palo Alto Hlth Care Syst, Phys Med & Rehabil Serv, Palo Alto, CA 94304 USA
关键词
analgesia; magnetic stimulation; spinal cord; opioid;
D O I
10.1016/S1388-2457(02)00122-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: High intensity magnetic stimulation (MS) applied over the skin can painlessly depolarize superficial and deep nerves and we aimed to evaluate the effectiveness of MS of spinal nerves in evoking a potent analgesic response. Methods: The MS was administered to adult male Sprague-Dawley rats using a Cadwell MES-10 high-speed magnetic stimulator. A Peltier device and von Frey fibers were used to determine heat and mechanical nociceptive responses of the rats. Results: A brief (5 min) course of MS over the rat's lumbosacral spine produced a long-lasting (30-40 min) and robust (80-90% maximum possible effect) hindpaw antinociceptive effect to both mechanical and heat stimuli. Spinal cord transected rats had intact hindpaw nociceptive withdrawal responses, but transection eliminated MS evoked antinociception, indicating a critical extrasegmental component in the mechanism of MS antinociceptive action. The opiate receptor antagonist naloxone (5 mg/kg, i.p.) completely blocked MS evoked antinociception, demonstrating an opioidergic mechanism for MS antinociception. The alpha(2) adrenoceptor antagonist atipamezole (5 mg/kg, i.p.) slightly reduced the MS antinociceptive response to heat and had no effect on MS antinociception for mechanical stimuli. Conclusions: These data indicate that MS can evoke a robust, long-lasting antinociceptive effect, which requires an intact supraspinal pathway and is opioidergic mediated. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:1006 / 1012
页数:7
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