Department of Psychological Science, Weber State University, Ogden, Utah, USA.
Behav Pharmacol. 2020 Sep;31(6):583-590. doi: 10.1097/FBP.0000000000000562.
Electronic cigarette use has significantly increased over the past decade. However, there is limited preclinical research on the behavioral and abuse-related effects of nicotine vapor inhalation in rodents. The present study evaluates the effects of repeated nicotine vapor inhalation in male and female mice using a nicotine behavioral sensitization model. Male and female C57BL/6 mice were administered vaporized nicotine (0-10.0 mg/ml) or the positive control of intraperitoneally administered nicotine (0.5 mg/kg) once daily for 5 days, and locomotor activity was assessed. Body temperatures were measured before and after nicotine vapor inhalation to assess hypothermia. Nicotine vapor inhalation (1.0-3.0 mg/ml) produced a dose-dependent behavioral sensitization effect and produced hypothermia in male and female mice. Nicotine (0.5 mg/kg) also produced significant behavioral sensitization. No sex differences were found for nicotine behavioral sensitization with either route of administration. Pretreatment with the nonselective nicotinic antagonist mecamylamine blocked the behavioral sensitization produced by 1.0 mg/ml of nicotine vapor inhalation. These results established that nicotine vapor inhalation produces behavioral sensitization in an inverted U-shaped curve that is similar to the effects of injected nicotine across several behavioral models. Additionally, pretreatment with mecamylamine demonstrated that nicotinic receptor activation was responsible for the behavioral sensitization produced by nicotine vapor inhalation and was not a conditioned response to the vapor. The methods used in the present study provide an additional behavioral approach for evaluating the behavioral effects of repeated nicotine vapor inhalation that allows the manipulation of several variables, including e-liquid oil blend, e-liquid flavors, puff duration, etc.
电子烟的使用在过去十年中显著增加。然而,关于尼古丁蒸气吸入在啮齿动物中的行为和滥用相关效应的临床前研究有限。本研究使用尼古丁行为敏化模型评估雄性和雌性小鼠中重复尼古丁蒸气吸入的效应。雄性和雌性 C57BL/6 小鼠每天接受一次雾化尼古丁(0-10.0 mg/ml)或腹腔内给予尼古丁(0.5 mg/kg)的阳性对照处理,评估运动活性。在尼古丁蒸气吸入前后测量体温,以评估体温过低。尼古丁蒸气吸入(1.0-3.0 mg/ml)产生了剂量依赖性的行为敏化效应,并导致雄性和雌性小鼠体温过低。尼古丁(0.5 mg/kg)也产生了显著的行为敏化。无论给予途径如何,尼古丁的行为敏化均未发现性别差异。非选择性烟碱受体拮抗剂美加明预处理阻断了 1.0 mg/ml 尼古丁蒸气吸入产生的行为敏化。这些结果确立了尼古丁蒸气吸入产生了类似于几种行为模型中注射尼古丁的行为敏化的倒 U 形曲线。此外,美加明预处理表明,烟碱受体激活是尼古丁蒸气吸入产生的行为敏化的原因,而不是对蒸气的条件反应。本研究中使用的方法提供了一种评估重复尼古丁蒸气吸入的行为效应的额外行为方法,允许操纵几个变量,包括电子烟油混合物、电子烟油口味、抽吸持续时间等。