Brady L S, Mansbach R S, Skurdal D N, Muldoon S M, Barrett J E
Life Sci. 1984 Dec 24;35(26):2593-600. doi: 10.1016/0024-3205(84)90026-2.
The effects of the benzodiazepine receptor antagonist, Ro 15-1788, were examined on analgesia induced by morphine after central (intracerebroventricular, i.c.v., or intrathecal, i.t.) and systemic administration. Analgesia was assessed in squirrel monkeys trained to respond under an electric shock titration procedure and in mice using the radiant heat tail-flick test. Central and systemic administration of morphine produced antinociceptive effects that were antagonized by 0.1 mg/kg of naloxone in both species. Ro 15-1788 antagonized the effects of morphine after central (i.c.v. or i.t.) administration but did not alter the effects of morphine given by the systemic route. This novel interaction suggests that Ro 15-1788 may be useful in pharmacologically separating neural substrates subserving opiate analgesia.
研究了苯二氮䓬受体拮抗剂Ro 15 - 1788对吗啡经中枢(脑室内或鞘内)及全身给药后诱导的镇痛作用的影响。采用电击滴定程序训练的松鼠猴和利用辐射热甩尾试验的小鼠来评估镇痛效果。吗啡经中枢及全身给药均产生了抗伤害感受作用,在这两个物种中,0.1mg/kg的纳洛酮均可拮抗该作用。Ro 15 - 1788可拮抗吗啡经中枢(脑室内或鞘内)给药后的作用,但不改变吗啡经全身途径给药的效果。这种新型相互作用表明,Ro 15 - 1788可能有助于从药理学上区分介导阿片类镇痛的神经底物。