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季铵型纳洛酮对吗啡诱导的纳洛酮效价增加的影响。

The effect of quaternary naloxone on the increased naloxone potency induced by morphine.

作者信息

Wong C L, Wai M K

出版信息

Clin Exp Pharmacol Physiol. 1984 Sep-Oct;11(5):467-71. doi: 10.1111/j.1440-1681.1984.tb00854.x.

Abstract

Using the abdominal constriction test in mice it was shown that the antinociceptive effect of morphine was inhibited by naloxone hydrochloride and its quaternary derivative naloxone methylbromide which presumably only acts peripherally. Pretreatment with a single dose of morphine 2.0 mg/kg s.c. did not alter the antinociceptive effect of a second dose of morphine given 3 h later. However, the antagonistic effect of naloxone against morphine was enhanced at this time. The development of increased naloxone potency was inhibited when naloxone hydrochloride was given together with morphine in the pretreatment. A similar inhibitory effect was observed when the quaternary derivative naloxone methylbromide was used instead of naloxone hydrochloride in the pretreatment regime. As there was no difference between the effects of naloxone hydrochloride and naloxone methylbromide in suppressing the development of increased naloxone potency induced by morphine pretreatment, it was concluded that this phenomenon may be mediated mainly through peripheral opiate receptors.

摘要

在小鼠身上使用腹部收缩试验表明,盐酸纳洛酮及其季铵衍生物甲基溴化纳洛酮(可能仅在外周起作用)可抑制吗啡的抗伤害感受作用。皮下注射单剂量2.0mg/kg吗啡进行预处理,不会改变3小时后给予的第二剂吗啡的抗伤害感受作用。然而,此时纳洛酮对吗啡的拮抗作用增强。在预处理中,当盐酸纳洛酮与吗啡一起给药时,纳洛酮效力增加的发展受到抑制。当在预处理方案中使用季铵衍生物甲基溴化纳洛酮代替盐酸纳洛酮时,观察到类似的抑制作用。由于盐酸纳洛酮和甲基溴化纳洛酮在抑制吗啡预处理诱导的纳洛酮效力增加的发展方面没有差异,因此得出结论,这种现象可能主要通过外周阿片受体介导。

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Increased antagonist potency of naloxone caused by morphine pretreatment in mice.
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