Spaulding T C, Fielding S, Venafro J J, Lal H
Eur J Pharmacol. 1979 Sep 1;58(1):19-25. doi: 10.1016/0014-2999(79)90335-2.
The activity of clonidine and its interaction with morphine was assessed in the mouse tail flick assay. In this assay, clonidine was found to be 10 times more potent than morphine. Clonidine potentiated morphine antinociceptive activity approximately five-fold and morphine potentiated clonidine activity four-fold. Clonidine's agonstic activity was not reversed by naloxone hydrochloride (10 mg/kg) while the potentiating effect of clonidine by morphine was. Tolerance to the antinociceptive effect of morphine was observed in morphine pellet-implanted mice but no cross tolerance was observed for clonidine. These data indicate that clonidine-induced analgesia is not a result of an interaction at morphine receptors; but rather, common pathway(s) are present which appear to complement the agonistic interaction of each.
在小鼠甩尾试验中评估了可乐定的活性及其与吗啡的相互作用。在该试验中,发现可乐定的效力是吗啡的10倍。可乐定使吗啡的抗伤害感受活性增强约5倍,而吗啡使可乐定的活性增强4倍。可乐定的激动活性不会被盐酸纳洛酮(10mg/kg)逆转,而吗啡对可乐定的增强作用会被逆转。在植入吗啡丸的小鼠中观察到对吗啡抗伤害感受作用的耐受性,但未观察到对可乐定的交叉耐受性。这些数据表明,可乐定诱导的镇痛不是吗啡受体相互作用的结果;相反,存在共同途径,似乎可补充各自的激动相互作用。