Schady W, Torebjörk H E
J Clin Pharmacol. 1984 Oct;24(10):429-35. doi: 10.1002/j.1552-4604.1984.tb01815.x.
The central analgesic activity of zomepirac was studied in six healthy subjects by means of intraneural electrical stimulation. Pain elicited by selective activation of nociceptive fibers was inhibited by the administration of a single oral dose of 100 mg zomepirac. Pain relief in this double-blind crossover study was significantly greater after zomepirac than after placebo. Maximal analgesic effect was observed between 30 and 90 minutes after ingestion. Since peripheral receptors are bypassed by this technique, it is postulated that the observed effect reflects a central action of zomepirac, possibly as a result of inhibition of prostaglandin synthesis in the central nervous system.
通过神经内电刺激研究了6名健康受试者中佐美酸的中枢镇痛活性。单次口服100mg佐美酸可抑制伤害性纤维选择性激活所引发的疼痛。在这项双盲交叉研究中,佐美酸给药后的疼痛缓解明显大于安慰剂。服药后30至90分钟观察到最大镇痛效果。由于该技术绕过了外周受体,推测观察到的效果反映了佐美酸的中枢作用,可能是由于中枢神经系统中前列腺素合成受到抑制。