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丙泊酚的行为学和毒理学效应。

Behavioral and toxicological effects of propofol.

作者信息

Gatch Michael B, Forster Michael J

机构信息

Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX 76107-2699, USA.

出版信息

Behav Pharmacol. 2011 Oct;22(7):718-22. doi: 10.1097/FBP.0b013e32834aff84.

Abstract

There is increasing concern about abuse of propofol, a widely-used surgical anesthetic and sedative that is currently not a controlled substance. The purpose of this study was to establish a rat model of the psychoactive effect of subanesthetic doses of propofol that could be useful for confirming abuse liability and for studying mechanisms of propofol abuse. Sprague-Dawley rats were trained to discriminate propofol (10 mg/kg, intraperitoneally) from vehicle (2% methylcellulose). Carisoprodol (100 mg/kg), chlordiazepoxide (10 mg/kg), and dizocilpine (0.1 mg/kg) were tested for substitution for the discriminative-stimulus effects of propofol (10 mg/kg), whereas pentylenetetrazol (10 mg/kg) was tested for antagonism of the discriminative-stimulus effects. Propofol (10 mg/kg) was tested for substitution in rats trained to discriminate carisoprodol from vehicle. Carisoprodol produced 59% propofol-appropriate responding, chlordiazepoxide produced 65% propofol-appropriate responding, and dizocilpine produced 34% propofol-appropriate responding. Pentylenetetrazol decreased propofol-appropriate responding to 41%. Propofol produced 52% carisoprodol-appropriate responding. Mortality rate during training of propofol (10 mg/kg) was 38%. Postmortem examination revealed cardiovascular abnormalities similar to those observed in propofol-infusion syndrome in humans. The results demonstrate that propofol can be trained as a discriminative stimulus. Its discriminative-stimulus effects were more similar to compounds promoting γ-aminobutyric acid-A receptor activity than to a compound inhibiting N-methyl-d-aspartate receptor activity. As propofol has discriminative-stimulus effects similar to known drugs of abuse, and occasions a high-mortality rate, its potential for continued abuse is of particular concern.

摘要

人们越来越关注丙泊酚的滥用问题。丙泊酚是一种广泛使用的外科麻醉剂和镇静剂,目前不属于管制药物。本研究的目的是建立一个亚麻醉剂量丙泊酚精神活性作用的大鼠模型,这可能有助于确认其滥用可能性并研究丙泊酚滥用的机制。将斯普拉格-道利大鼠训练成能够区分丙泊酚(10毫克/千克,腹腔注射)和赋形剂(2%甲基纤维素)。测试了卡立普多(100毫克/千克)、氯氮卓(10毫克/千克)和地佐环平(0.1毫克/千克)对丙泊酚(10毫克/千克)辨别刺激效应的替代作用,而测试了戊四氮(10毫克/千克)对丙泊酚辨别刺激效应的拮抗作用。对训练成能够区分卡立普多和赋形剂的大鼠测试了丙泊酚(10毫克/千克)的替代作用。卡立普多产生了59%与丙泊酚相符的反应,氯氮卓产生了65%与丙泊酚相符的反应,地佐环平产生了34%与丙泊酚相符的反应。戊四氮将与丙泊酚相符的反应降低到41%。丙泊酚产生了52%与卡立普多相符的反应。丙泊酚(10毫克/千克)训练期间的死亡率为38%。尸检显示心血管异常,类似于人类丙泊酚输注综合征中观察到的情况。结果表明丙泊酚可以被训练为一种辨别刺激。其辨别刺激效应与促进γ-氨基丁酸-A受体活性的化合物比与抑制N-甲基-D-天冬氨酸受体活性的化合物更相似。由于丙泊酚具有与已知滥用药物相似的辨别刺激效应,且导致高死亡率,其持续滥用的可能性尤其令人担忧。

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