Aleman V, de Muñoz D M
Exp Neurol. 1983 May;80(2):451-6. doi: 10.1016/0014-4886(83)90296-0.
An investigation was made of the effect of morphine dependence on the characteristics of seizures induced in mice by convulsant drugs with differing mechanisms of action. Morphine dependence was induced in 90-day-old mice (weighing 29 to 32 g) by a 6-day schedule of twice daily i.p. injections of increasing doses of morphine (5, 32.5, 58, 82.5, 100, and 135 mg kg-1). Thirty minutes after the last morphine administration, convulsant drugs (4-aminopyridine 8 mg kg-1, pentylenetetrazol 50 mg kg-1, bicuculline 2.5 mg kg-1, strychnine 2.0 mg kg-1, and beta-mercaptopropionic acid 50 mg kg-1) were injected. 4-Aminopyridine (4-AP) and pentylenetetrazol (PTZ) increased both the number of animals with convulsions and death and in the case of 4-AP the period of convulsion latency was also increased. Naloxone at 1.0 mg kg-1 blocked the 4-AP effects, indicating that this action was mediated through an opioid receptor. Strychnine and beta-mercaptopropionic acid had an effect opposite 4-AP and PTZ in the number of animals with convulsions and death. On the other hand bicuculline had an effect more like 4-AP and PTZ than other inhibitory synapse-blocking drugs. We conclude that chronic morphine treatment modified the response of convulsant drugs depending on their mechanisms of action.
研究了吗啡依赖对作用机制不同的惊厥药物诱发小鼠惊厥特征的影响。通过6天的给药方案,每天两次腹腔注射递增剂量的吗啡(5、32.5、58、82.5、100和135 mg·kg⁻¹),使90日龄小鼠(体重29至32 g)产生吗啡依赖。在最后一次注射吗啡30分钟后,注射惊厥药物(4-氨基吡啶8 mg·kg⁻¹、戊四氮50 mg·kg⁻¹、荷包牡丹碱2.5 mg·kg⁻¹、士的宁2.0 mg·kg⁻¹和β-巯基丙酸50 mg·kg⁻¹)。4-氨基吡啶(4-AP)和戊四氮(PTZ)增加了惊厥和死亡动物的数量,并且就4-AP而言,惊厥潜伏期也延长了。1.0 mg·kg⁻¹的纳洛酮阻断了4-AP的作用,表明该作用是通过阿片受体介导的。士的宁和β-巯基丙酸在惊厥和死亡动物数量上的作用与4-AP和PTZ相反。另一方面,荷包牡丹碱与其他抑制性突触阻断药物相比,其作用更类似于4-AP和PTZ。我们得出结论,慢性吗啡治疗根据惊厥药物的作用机制改变了它们的反应。