Winter C A, Kling P J, Tocco D J, Tanabe K
J Pharmacol Exp Ther. 1979 Dec;211(3):678-85.
A method is described for testing analgesia for narcotic or nonnarcotic drugs in rats injected with Freund's adjuvant in the tail, by manipulation of the tail the day after injection, or of the feet after the development of adjuvant arthritis. The method is responsive to a behavioral depressant or an anti-inflammatory steroid. Diflunisal (MK-647; 5-(2,4-difluorophenyl)salicylic acid] exhibited activity in this assay after oral administration with potency about 25 times greater than that of aspirin, about 3 times that of glafenine and twice that of zomepirac. The onset of activity was within a 1/2 hour for narcotic analgesics but required about an hour for non-narcotic compounds. With the latter, the peak of activity was not attained until 2 to 4 hr, depending on the compound. The peak for diflunisal was delayed until the 3rd or 4th hour, but the onset of action was more prompt and the duration greater as the dose was increased. [14C]Diflunisal was concentrated to some extent in the inflamed tissue after adjuvant injection. Peak levels both in plasma and tissue appeared about 2 hr before peak analgesic effect. Repeated administration of large doses produced neither tolerance nor sensitization to the analgesic action of diflunisal. Naloxone and naltrexone did not antagonize the action of the compound, but when morphine and diflunisal were given together, the overall effect was enhanced.
本文描述了一种在大鼠尾部注射弗氏佐剂后测试麻醉性或非麻醉性药物镇痛作用的方法,即在注射后第二天通过操纵尾巴,或在佐剂性关节炎发展后通过操纵足部来进行测试。该方法对行为抑制剂或抗炎类固醇有反应。双氟尼酸(MK - 647;5 -(2,4 - 二氟苯基)水杨酸)口服给药后在该试验中表现出活性,其效力约为阿司匹林的25倍,约为格拉非宁的3倍,佐美酸的2倍。麻醉性镇痛药的活性起效时间在半小时内,但非麻醉性化合物则需要约一小时。对于后者,根据化合物的不同,活性峰值直到2至4小时才达到。双氟尼酸的峰值延迟到第3或第4小时,但起效更快,且随着剂量增加持续时间更长。[14C]双氟尼酸在佐剂注射后在炎症组织中有所蓄积。血浆和组织中的峰值水平在镇痛作用峰值出现前约2小时出现。重复给予大剂量药物既不会产生对双氟尼酸镇痛作用的耐受性,也不会产生致敏作用。纳洛酮和纳曲酮不会拮抗该化合物的作用,但当吗啡和双氟尼酸一起给药时,总体效果会增强。