Marusov I V, Marusova I B, Pchelintsev M V
Valdman Institute of Pharmacology, Pavlov State Medical University, ul. L. Tolstogo 6/8, St. Petersburg, 197022 Russia.
Eksp Klin Farmakol. 2001 Jan-Feb;64(1):30-2.
Peroral administration of lornoxicam, a new representative of the class of oxicams, in a total dose of 2-16 mg/kg produced a dose-dependent analgesic effect in rats with formalin-induced tail inflammation, as confirmed by the tail-flick and hot-plate tests. The maximum analgesic effect of lornoxicam during the formalin-induced edema development was observed upon a three-fold drug administration by the scheme 1/2, 1/4, 1/4 of the total dose (8-16 mg/kg, p.o.) with a 3 h interval prior to formalin injection into the rat tail base. Validity of using the tail-flick and hot-plate methods for evaluation of the analgesic effect of NSAID is discussed.
口服给予昔康类的新代表药物氯诺昔康,总剂量为2-16mg/kg,在福尔马林诱导大鼠尾部炎症模型中产生剂量依赖性镇痛作用,甩尾试验和热板试验证实了这一点。在福尔马林诱导的水肿形成过程中,氯诺昔康的最大镇痛作用是通过在向大鼠尾根部注射福尔马林前3小时按照1/2、1/4、1/4的总剂量方案(8-16mg/kg,口服)给药三次观察到的。讨论了使用甩尾法和热板法评估非甾体抗炎药镇痛作用的有效性。