Kavaliers M, Ossenkopp K P
Bioelectromagnetics Western and Neuroscience Program, University of Western Ontario, London, Canada.
Brain Res. 1993 Aug 20;620(1):159-62. doi: 10.1016/0006-8993(93)90285-u.
Results of studies with rodents have shown that animals repeatedly injected with the opioid antagonist, naloxone, acquire a hypoalgesic response to thermal nociceptive stimuli. The present study revealed a similar response in the terrestrial pulmonate snail, Cepaea nemoralis. Snails receiving daily injections of naloxone followed by measurements of thermal nociceptive sensitivity also developed hypoalgesia. Daily brief (30-min) exposures to a weak 60-Hz magnetic field (1.0 gauss or 0.1 mT), which acutely antagonize opioid-mediated nociception and antinociception in a manner comparable to that of naloxone, also led to the expression of a hypoalgesic responses. This suggests that opioid antagonist-induced thermal hypoalgesia may be a basic feature of opioid systems. This naloxone- and magnetic field-induced 'analgesia' is consistent with either a facilitation of aversive thermal conditioning and or antagonism of the excitatory, hyperalgesic effects of low levels of endogenous opioids.
对啮齿动物的研究结果表明,反复注射阿片类拮抗剂纳洛酮的动物会对热痛觉刺激产生痛觉减退反应。本研究揭示了陆生肺螺类蜗牛(黄斑蛞蝓)也有类似反应。每天接受纳洛酮注射后测量热痛觉敏感性的蜗牛也出现了痛觉减退。每天短暂(30分钟)暴露于弱60赫兹磁场(1.0高斯或0.1毫特斯拉),其以与纳洛酮相当的方式急性拮抗阿片类介导的痛觉和抗痛觉,也导致了痛觉减退反应的表达。这表明阿片类拮抗剂诱导的热痛觉减退可能是阿片类系统的一个基本特征。这种纳洛酮和磁场诱导的“镇痛”与厌恶热条件反射的促进和/或内源性阿片类药物低水平的兴奋性、痛觉过敏作用的拮抗是一致的。