Nickel B, Engel J, Szelenyi I
Department of Pharmacology, ASTA Pharma AG, Frankfurt, Federal Republic of Germany.
Agents Actions. 1988 Feb;23(1-2):112-6. doi: 10.1007/BF01967209.
These experimental studies were conducted to obtain information about the antinociceptive action of flupirtine within the central nervous system. Flupirtine dose-dependently increased pain threshold in the electrostimulated pain test in mice. Its antinociceptive activity was attenuated by simultaneous administration of the noradrenergic alpha 1/alpha 2-antagonist yohimbine and alpha 2-antagonist idazoxane. By contrast, the analgesia induced by codeine or morphine was not influenced by alpha 2-adrenergic antagonists at all. A striking resemblance could be observed in the pharmaco-EEG of freely moving rats treated with clonidine and flupirtine, respectively. The present results are consistent with the hypothesis that the noradrenergic descending pain-modulating system might be involved in the antinociceptive mode of action of flupirtine.
进行这些实验研究是为了获取有关氟吡汀在中枢神经系统中的抗伤害感受作用的信息。在小鼠的电刺激疼痛试验中,氟吡汀剂量依赖性地提高了疼痛阈值。同时给予去甲肾上腺素能α1/α2拮抗剂育亨宾和α2拮抗剂伊达唑新可减弱其抗伤害感受活性。相比之下,可待因或吗啡诱导的镇痛作用完全不受α2肾上腺素能拮抗剂的影响。分别用可乐定和氟吡汀处理的自由活动大鼠的药物脑电图中可观察到显著相似性。目前的结果与去甲肾上腺素能下行疼痛调节系统可能参与氟吡汀抗伤害感受作用模式的假说一致。