Gardell L R, Burgess S E, Dogrul A, Ossipov M H, Malan T P, Lai J, Porreca F
Department of Pharmacology, University of Arizona Health Sciences Center, Tucson, AZ 85724, USA.
Pain. 2002 Jul;98(1-2):79-88. doi: 10.1016/s0304-3959(01)00475-4.
Recent studies indicate that sustained opioid administration produces increased expression of spinal dynorphin, which promotes enhanced sensitivity to non-noxious and noxious stimuli. Such increased "pain" may manifest behaviorally as a decrease in spinal antinociceptive potency. Here, the possibility of similar mechanisms in the antinociception of spinal cannabinoids was explored. Response thresholds to non-noxious mechanical and noxious thermal stimuli were assessed. Antinociception was determined using the 52 degrees C tail-flick test. Mice received repeated WIN 55,212-2, its inactive enantiomer, WIN 55,212-3 or vehicle (i.th., bid, 5 days). WIN 55,212-2, but not WIN 55,212-3 or vehicle, produced a time-related increased sensitivity to non-noxious and noxious stimuli. WIN 55,212-2, but not WIN 55,212-3 or vehicle, elicited a significant increase in lumbar spinal dynorphin content at treatment day 5. Increased sensitivity to mechanical and thermal stimuli produced by WIN 55,212-2 was reversed to baseline levels by i.th. MK-801 or dynorphin antiserum; control serum had no effect. WIN 55,212-2, but not WIN 55,212-3 or vehicle, produced dose-related antinociception and repeated administration resulted in antinociceptive tolerance. While MK-801 and dynorphin antiserum did not alter acute antinociception produced by WIN 55,212-2, these substances significantly blocked antinociceptive tolerance when given immediately prior to WIN 55,212-2 challenge on day 5. Daily MK-801 pretreatments, prior to WIN 55,212-2 injection, also produced a significant block of antinociceptive tolerance. These data suggest that like opioids, repeated spinal administration of a cannabinoid CB1 agonist elicits abnormal pain, which results in increased expression of spinal dynorphin. Manipulations that block cannabinoid-induced pain also block the behavioral manifestation of cannabinoid tolerance.
最近的研究表明,持续给予阿片类药物会使脊髓强啡肽的表达增加,这会促进对非伤害性和伤害性刺激的敏感性增强。这种增加的“疼痛”在行为上可能表现为脊髓抗伤害感受能力的下降。在此,探讨了脊髓大麻素抗伤害感受中类似机制的可能性。评估了对非伤害性机械刺激和伤害性热刺激的反应阈值。使用52摄氏度甩尾试验确定抗伤害感受。小鼠接受重复给予WIN 55,212-2、其无活性对映体WIN 55,212-3或赋形剂(鞘内注射,每日两次,共5天)。WIN 55,212-2,但不是WIN 55,212-3或赋形剂,产生了与时间相关的对非伤害性和伤害性刺激的敏感性增加。WIN 55,212-2,但不是WIN 55,212-3或赋形剂,在治疗第5天时引起腰椎脊髓强啡肽含量显著增加。WIN 55,212-2所产生的对机械和热刺激的敏感性增加通过鞘内注射MK-801或强啡肽抗血清恢复到基线水平;对照血清无作用。WIN 55,212-2,但不是WIN