Hueza Isis M, Ponce Fernando, Garcia Raphael C T, Marcourakis Tânia, Yonamine Maurício, Mantovani Cínthia de C, Kirsten Thiago B
Institute of Environmental, Chemical and Pharmaceutical Sciences, Federal University of São Paulo (ICAQF-UNIFESP), Diadema, S.P., Brazil; Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, S.P., Brazil.
Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, S.P., Brazil.
J Pharmacol Toxicol Methods. 2016 Jan-Feb;77:17-23. doi: 10.1016/j.vascn.2015.09.003. Epub 2015 Sep 25.
The use of smoked illicit drugs has spread dramatically, but few studies use proper devices to expose animals to inhalational abused drugs despite the availability of numerous smoking devices that mimic tobacco exposure in rodents. Therefore, the present study developed an inexpensive device to easily expose laboratory animals to smoked drugs. We used crack cocaine as the drug of abuse, and the cocaine plasma levels and the behaviors of animals intoxicated with the crack cocaine were evaluated to prove inhaled drug absorption and systemic activity. We developed an acrylic device with two chambers that were interconnected and separated by a hatch. Three doses of crack (100, 250, or 500 mg), which contained 63.7% cocaine, were burned in a pipe, and the rats were exposed to the smoke for 5 or 10 min (n=5/amount/period). Exposure to the 250-mg dose for 10 min achieved cocaine plasma levels that were similar to those of users (170 ng/mL). Behavioral evaluations were also performed to validate the methodology. Rats (n=10/group) for these evaluations were exposed to 250 mg of crack cocaine or air for 10 min, twice daily, for 28 consecutive days. Open-field evaluations were performed at three different periods throughout the experimental design. Exposed animals exhibited transient anorexia, increased motor activity, and shorter stays in central areas of the open field, which suggests reduced anxiety. Therefore, the developed model effectively exposed animals to crack cocaine, and this model may be useful for the investigation of other inhalational abused drugs.
吸食非法毒品的现象已急剧蔓延,但尽管有许多可模拟啮齿动物烟草暴露的吸烟装置,却很少有研究使用合适的装置让动物接触吸入性滥用药物。因此,本研究开发了一种廉价装置,可轻松让实验动物接触吸食的毒品。我们使用快克可卡因作为滥用药物,并评估了可卡因的血浆水平以及吸食快克可卡因的动物的行为,以证明吸入药物的吸收和全身活性。我们开发了一种丙烯酸装置,它有两个相互连接的腔室,由一个舱口隔开。将含有63.7%可卡因的三个剂量的快克(100、250或500毫克)在烟斗中燃烧,让大鼠接触烟雾5或10分钟(每组剂量/时间段n = 5)。接触250毫克剂量10分钟后,可卡因血浆水平与使用者相似(170纳克/毫升)。还进行了行为评估以验证该方法。用于这些评估的大鼠(每组n = 10)连续28天每天两次接触250毫克快克可卡因或空气10分钟。在整个实验设计的三个不同时间段进行旷场评估。接触毒品的动物表现出短暂的厌食、运动活动增加以及在旷场中央区域停留时间缩短,这表明焦虑减轻。因此,所开发的模型有效地让动物接触了快克可卡因,该模型可能有助于研究其他吸入性滥用药物。