Contreras E, Tamayo L, Quijada L
Arch Int Pharmacodyn Ther. 1977 Aug;228(2):293-9.
Several drugs affecting nerve cell excitability, by opposing ion movements in membranes, were tested in mice rendered tolerant to or dependent on morphine. The purpose of the study was to investigate whether these drugs share the ability to attenuate morphine tolerance and dependence exhibited by tricyclic antidepressants. Tolerance to morphine was decreased by the administration of imipramine, doxepin, promethazine, propranolol, lidocaine and quinidine. Chlorpromazine and carbamazepine were ineffective. The intensity of the abstinence syndrome provoked by naloxone was decreased by chlorpromazine, imipramine, doxepin, lidocaine, quinidine and propranolol. Diphenyl. hydantion and carbamazepine had no effect. The results are discussed in relation with the blockade of ion conductance and their interference with the release of neurotransmitters produced by the drugs assayed.
通过对抗细胞膜中的离子运动来影响神经细胞兴奋性的几种药物,在对吗啡产生耐受性或依赖性的小鼠身上进行了测试。该研究的目的是调查这些药物是否具有与三环类抗抑郁药相同的减轻吗啡耐受性和依赖性的能力。给予丙咪嗪、多塞平、异丙嗪、普萘洛尔、利多卡因和奎尼丁可降低对吗啡的耐受性。氯丙嗪和卡马西平无效。氯丙嗪、丙咪嗪、多塞平、利多卡因、奎尼丁和普萘洛尔可降低纳洛酮诱发的戒断综合征的强度。苯妥英和卡马西平没有效果。结合所测药物对离子电导的阻断及其对神经递质释放的干扰对结果进行了讨论。