Manson H J, Dyke G, Melling J, Gough M
Can Anaesth Soc J. 1983 Jan;30(1):28-31. doi: 10.1007/BF03007713.
The incidence of withdrawal convulsions was determined in mice following removal from a 70 per cent nitrous oxide environment. Groups of 20 mice received saline (control), naloxone or morphine subcutaneous injections five minutes prior to withdrawal. The observer was blind to the treatments. In comparison to the control group, the proportion convulsing was significantly (p less than 0.05) increased following naloxone 0.125 mg (n = 40), 0.25 mg, but not 0.5 mg. The proportion convulsing was significantly decreased following morphine 0.4 mg. Overall proportions of mice convulsing was 0.55 for the saline control group; 0.73 for naloxone 0.125 mg; 0.80 for naloxone 0.25 mg; 0.60 for naloxone 0.50 mg; and 0.38 for morphine 0.4 mg. Modification of this phenomenon by both an opiate antagonist and agonist suggests endorphin withdrawal as a possible mechanism. However, this should be regarded as indirect evidence pending further study of this area.
在将小鼠从70%氧化亚氮环境中移出后,测定戒断性惊厥的发生率。20只小鼠为一组,在戒断前5分钟皮下注射生理盐水(对照组)、纳洛酮或吗啡。观察人员对处理情况不知情。与对照组相比,注射0.125毫克(n = 40)、0.25毫克而非0.5毫克纳洛酮后,惊厥比例显著升高(p小于0.05)。注射0.4毫克吗啡后,惊厥比例显著降低。生理盐水对照组小鼠惊厥的总体比例为0.55;0.125毫克纳洛酮组为0.73;0.25毫克纳洛酮组为0.80;0.50毫克纳洛酮组为0.60;0.4毫克吗啡组为0.38。阿片类拮抗剂和激动剂对这一现象的改变表明内啡肽戒断可能是一种机制。然而,在该领域进一步研究之前,这应被视为间接证据。