Davis A, Perkins M N
Sandoz Institute for Medical Research, London, UK.
Agents Actions. 1993;38 Spec No:C10-2. doi: 10.1007/BF01991121.
Systemic administration of capsaicin has been shown to be antinociceptive in a number of acute nociceptive models. We present here two models of prolonged hyperalgesia in the rat induced by intra-articular injection of uric acid or Freund's complete adjuvant into the knee. The time course of hyperalgesia lasts up to 48 h with uric acid and 5 to 10 days with Freund's adjuvant. The hyperalgesia was maximal in both models after 18 h. At this time, the weight tolerated by the injected leg was reduced by 70-80% in the Freund's-treated and 50-60% in the uric-treated animals, compared to the uninjected leg. The hyperalgesia was reversed in both models by indomethacin and ibuprofen (1-100 mg kg-1 s.c.), paracetamol (50-500 mg kg-1 s.c.) and morphine (2-16 mg kg-1 s.c.) in a dose-dependent manner. The morphine reversal was blocked by coadministration with naloxone (2.5 mg kg-1 s.c.). Capsaicin (3-9 mg kg-1 s.c.) also reversed the hyperalgesia in both models.
在多种急性伤害性感受模型中,已证明辣椒素的全身给药具有抗伤害感受作用。我们在此展示两种大鼠长期痛觉过敏模型,通过向膝关节内注射尿酸或弗氏完全佐剂诱导。尿酸诱导的痛觉过敏时程长达48小时,弗氏佐剂诱导的痛觉过敏时程为5至10天。两种模型在18小时后痛觉过敏达到最大程度。此时,与未注射的腿相比,弗氏佐剂处理组动物注射腿的承重减少70 - 80%,尿酸处理组动物注射腿的承重减少50 - 60%。吲哚美辛、布洛芬(1 - 100毫克/千克,皮下注射)、对乙酰氨基酚(50 - 500毫克/千克,皮下注射)和吗啡(2 - 16毫克/千克,皮下注射)以剂量依赖方式逆转了两种模型中的痛觉过敏。吗啡的逆转作用可被与纳洛酮(2.5毫克/千克,皮下注射)共同给药所阻断。辣椒素(3 - 9毫克/千克,皮下注射)也逆转了两种模型中的痛觉过敏。