Vitale G, Sandrini M, Pini L A
Clinical Pharmacology Department, University of Modena, Italy.
Agents Actions. 1994 May;41(3-4):184-7. doi: 10.1007/BF02001914.
An increasing number of observations indicate that prostaglandin synthesis inhibition is not a satisfactory explanation for the antinociceptive activity of the non-steroidal anti-inflammatory drugs. In the hot-plate test performed 1 or 2 h after ketorolac at 40, 70 and 100 mg/kg i.p., the drug does not display any significant antinociceptive activity. Nor, at the two higher doses used, does it affect the cortical and pontine serotonin binding capacity of rat brain membranes 2 h after treatment. The data suggest that this lack of anti-nociceptive activity in the hot-plate test is associated with the drug's inability to affect the central serotoninergic system.
越来越多的观察结果表明,前列腺素合成抑制并不能令人满意地解释非甾体抗炎药的抗伤害感受活性。在腹腔注射酮咯酸40、70和100mg/kg后1或2小时进行的热板试验中,该药物未表现出任何显著的抗伤害感受活性。在使用的两个较高剂量下,治疗后2小时它也不影响大鼠脑膜的皮质和脑桥5-羟色胺结合能力。数据表明,热板试验中这种缺乏抗伤害感受活性与该药物无法影响中枢5-羟色胺能系统有关。