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阿片类镇痛药曲马多可引起肌肉强直,而非阿片类药物氟吡汀则不会。

Muscle rigidity induced by the opioid analgesic tramadol, but not by the non-opioid flupirtine.

作者信息

Ossowska K, Wolfarth S

机构信息

Department of Neuro-Psychopharmacology, Polish Academy of Sciences, Kraków.

出版信息

Pol J Pharmacol. 1994 Jan-Apr;46(1-2):61-5.

PMID:7981773
Abstract

The influence of high doses of two analgesic drugs, tramadol and flupirtine on the electromyographic activity in the gastrocnemius soleus muscles was examined. Tramadol (100-200 mg/kg po) dose-dependently induced a tonic electromyographic activity, which is generally accepted as a model of the opiate-induced muscle rigidity. That effect was antagonized by intraperitoneal injection of naloxone (0.8 mg/kg ip). On the other hand, flupirtine even in the high doses (100-200 mg/kg po) did not induce any tonic electromyographic activity. The obtained results confirm an opiate-like action of tramadol, but not that of flupirtine, on the muscle tension.

摘要

研究了两种镇痛药物曲马多和氟吡汀的高剂量对腓肠肌比目鱼肌肌电活动的影响。曲马多(100 - 200毫克/千克口服)剂量依赖性地诱发强直性肌电活动,这通常被认为是阿片类药物诱发肌肉强直的模型。腹腔注射纳洛酮(0.8毫克/千克腹腔注射)可拮抗该效应。另一方面,即使是高剂量(100 - 200毫克/千克口服)的氟吡汀也未诱发任何强直性肌电活动。所得结果证实了曲马多对肌肉张力具有阿片样作用,而氟吡汀则没有。

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