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(±)-、(+)-和(-)-奈福泮对小鼠的镇痛作用。

Antinociceptive effects of (+/-)-, (+)- and (-)-nefopam in mice.

作者信息

Fasmer O B, Berge O G, Jørgensen H A, Hole K

出版信息

J Pharm Pharmacol. 1987 Jul;39(7):508-11. doi: 10.1111/j.2042-7158.1987.tb03167.x.

Abstract

The antinociceptive activity of (+/-)-, (+)- and (-)-nefopam in mice has been examined using the hot-plate, formalin and tail-flick tests. Nefopam was administered by the intraperitoneal, intracerebroventricular (i.c.v.) and intrathecal (i.th.) routes. Intraperitoneal injection of (+/-)-nefopam (10-20 mg kg-1) had powerful analgesic effects in the hot-plate and formalin tests. In the tail-flick test it produced a weak, but significant elevation of the response latencies. In spinalized animals, however, the effect was abolished, indicating that nefopam prolonged the tail-flick latencies by activation of descending pain-modulating pathways. (+/-)-Nefopam (5-20 micrograms) elicited analgesia in the hot-plate test after i.c.v. or i.th. injection. These findings suggest that nefopam has both a spinal and a supraspinal site of action. (+)-Nefopam was significantly more potent than (-)-nefopam after both systemic and central administration.

摘要

已使用热板法、福尔马林法和甩尾法测试了(±)-、(+)-和(-)-奈福泮在小鼠中的抗伤害感受活性。奈福泮通过腹腔内、脑室内(i.c.v.)和鞘内(i.th.)途径给药。腹腔注射(±)-奈福泮(10 - 20 mg kg⁻¹)在热板法和福尔马林法测试中具有强大的镇痛作用。在甩尾法测试中,它使反应潜伏期产生微弱但显著的延长。然而,在脊髓横断的动物中,这种作用被消除,表明奈福泮通过激活下行性疼痛调节通路来延长甩尾潜伏期。脑室内或鞘内注射(±)-奈福泮(5 - 20微克)在热板法测试中引起镇痛作用。这些发现表明奈福泮具有脊髓和脊髓上的作用部位。全身给药和中枢给药后,(+)-奈福泮的效力均显著高于(-)-奈福泮。

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