Fabbri A, Cruccu G, Sperti P, Ridolfi M, Ciampani T, Leardi M G, Ferracuti S, Bonifacio V
Chair of Andrology, Vth Medical Clinic, Rome, Italy.
Experientia. 1992 Dec 1;48(11-12):1139-42. doi: 10.1007/BF01948008.
Piroxicam is a nonsteroidal anti-inflammatory drug with a potent analgesic effect. In order to establish whether the analgesic action of Piroxicam has a central component, we studied the effect of the drug on the nociceptive orbicularis oculi reflexes evoked by electrical stimulation of the cornea and supraorbital nerve in healthy subjects. Piroxicam significantly suppressed the corneal reflex and R3 component of the blink reflex by 28% (p < 0.05) and 50% (p < 0.01), respectively. This effect was not reversed by the i.v. injection of naloxone. Beta-endorphin levels did not change. Piroxicam administration induces distinct inhibitory changes in nociceptive reflexes, which suggests that the analgesic action of the drug has a central component. The ineffectiveness of naloxone, and the lack of beta-endorphin changes, indicate that this central action is independent of the opioid system; other pain regulatory systems are probably involved.
吡罗昔康是一种具有强效镇痛作用的非甾体抗炎药。为了确定吡罗昔康的镇痛作用是否有中枢成分,我们研究了该药物对健康受试者角膜和眶上神经电刺激诱发的伤害性眼轮匝肌反射的影响。吡罗昔康分别使角膜反射和瞬目反射的R3成分显著抑制了28%(p < 0.05)和50%(p < 0.01)。静脉注射纳洛酮并未逆转这种作用。β-内啡肽水平没有变化。给予吡罗昔康可引起伤害性反射明显的抑制性变化,这表明该药物的镇痛作用有中枢成分。纳洛酮无效以及β-内啡肽水平无变化表明这种中枢作用独立于阿片系统;可能涉及其他疼痛调节系统。