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新型5-羟色胺/去甲肾上腺素摄取抑制剂(Ro 15-8081)分级口服剂量与60毫克可待因及安慰剂相比,对健康男性实验性诱导疼痛及副作用情况的影响。

Effects of graded oral doses of a new 5-hydroxytryptamine/noradrenaline uptake inhibitor (Ro 15-8081) in comparison with 60 mg codeine and placebo on experimentally induced pain and side effect profile in healthy men.

作者信息

Stacher G, Steinringer H, Schneider S, Mittelbach G, Gaupmann G, Abatzi T A, Stacher-Janotta G

机构信息

Department of Psychiatry, University of Vienna, Austria.

出版信息

Br J Clin Pharmacol. 1987 Nov;24(5):627-35. doi: 10.1111/j.1365-2125.1987.tb03222.x.

Abstract
  1. Ro 15-8081 (Hoffmann-La Roche, Basle, Switzerland) is a novel mixed 5-HT/noradrenaline uptake inhibitor producing potent antinociceptive effects in animal pain models. 2. In healthy man, two models with electrically and thermally induced pain, respectively, have been shown to reliably discriminate between the effects of opioid as well as of antipyretic analgesics and placebo. 3. This study investigated the effects of single oral doses of 10, 25, and 50 mg Ro 15-8081 in comparison with 60 mg codeine and placebo on threshold and tolerance to electrically induced pain and on threshold to thermally induced pain. Furthermore, the effects on psychomotor function, self-rated subjective feelings, and side effect profile were studied. 4. Twenty healthy males participated each in five experiments in which they received, in random double-blind fashion, each of the treatments. Every experiment comprised two series of measurements before and twelve after drug administration, carried out at 30 min intervals. 5. Ro 15-8081 produced marked elevations of threshold and tolerance to electrically and of threshold to thermally induced pain. The effects of all doses of Ro 15-8081 were significantly superior to those of placebo. Threshold and tolerance to electrically induced pain were not affected differently by the three doses of Ro 15-8081, whereas the threshold to thermally induced pain was elevated significantly more by 50 mg than by 10 and 25 mg Ro 15-8081. 6. Codeine 60 mg had a more rapid onset of action and greater maximal effects than Ro 15-8081.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 罗15 - 8081(瑞士巴塞尔霍夫曼 - 罗氏公司)是一种新型的5 - 羟色胺/去甲肾上腺素混合摄取抑制剂,在动物疼痛模型中具有强效的抗伤害感受作用。2. 在健康人体中,分别采用电刺激和热刺激诱导疼痛的两种模型,已被证明能够可靠地区分阿片类药物、解热镇痛药和安慰剂的效果。3. 本研究调查了单次口服10毫克、25毫克和50毫克罗15 - 8081与60毫克可待因及安慰剂相比,对电刺激诱导疼痛的阈值和耐受性以及热刺激诱导疼痛阈值的影响。此外,还研究了对精神运动功能、自我评定的主观感受及副作用情况的影响。4. 20名健康男性分别参与了五项实验,他们以随机双盲方式接受每种治疗。每项实验在给药前和给药后12次进行测量,每隔30分钟进行一系列测量。5. 罗15 - 8081使电刺激诱导疼痛的阈值和耐受性以及热刺激诱导疼痛的阈值显著提高。罗15 - 8081所有剂量的效果均显著优于安慰剂。罗15 - 8081的三个剂量对电刺激诱导疼痛的阈值和耐受性影响无差异,而热刺激诱导疼痛的阈值,50毫克罗15 - 8081比10毫克和25毫克罗15 - 8081显著提高得更多。6. 60毫克可待因的起效更快,最大效果比罗15 - 8081更强。(摘要截选至250字)

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