RTI International, 3040 Cornwallis Road, Research Triangle Park, NC 27709-2194, United States.
RTI International, 3040 Cornwallis Road, Research Triangle Park, NC 27709-2194, United States.
Drug Alcohol Depend. 2019 Nov 1;204:107504. doi: 10.1016/j.drugalcdep.2019.06.007. Epub 2019 Aug 24.
Use of electronic cigarettes (e-cigarettes) has increased exponentially since their appearance on the U.S. market around 2007. To provide preclinical models of vaping that incorporate olfactory cues and chemosensory effects (including flavors) that play a role in human vaping behavior, the feasibility of using a modified e-cigarette device for delivery of aerosolized nicotine was examined in a nicotine discrimination procedure in mice.
Adult female and male C57BL/6 mice were trained to discriminate 0.75 mg/kg subcutaneous (s.c.) nicotine from saline. After determination of a s.c. nicotine dose-effect curve, aerosolized freebase nicotine and nicotine-containing tobacco products (i.e., non-flavored and Arctic Blast e-liquids) were evaluated.
Nicotine (s.c.) dose-dependently substituted in mice of both sexes, although females showed less sensitivity and greater variability. By contrast, aerosolized nicotine, regardless of formulation, produced concentration-dependent increases up to maximum of 46-62% nicotine-associated responding. Brain nicotine concentrations for each sex were similar for s.c. 0.75 mg/kg nicotine and 30 mg/ml freebase nicotine.
Mice of both sexes readily acquired s.c. nicotine discrimination, but females showed less sensitivity. Further, all three formulations of aerosolized nicotine produced increases in nicotine-like responding in mice of each sex. However, the maximum magnitude of these increases did not engender a similar degree of substitution as s.c. 0.75 mg/kg nicotine, despite similar brain concentrations of nicotine at 30 mg/ml aerosolized nicotine. Additional research is needed for determination of the reason(s); however, results here demonstrate initial feasibility for examination of the discriminative stimulus effects of vaped drugs such as nicotine.
自 2007 年美国市场出现电子烟以来,其使用呈指数级增长。为了提供包含嗅觉线索和化学感觉效应(包括口味)的蒸气作用的临床前模型,这些在人类蒸气作用行为中发挥作用,研究人员在小鼠尼古丁辨别程序中检查了使用改良电子烟装置输送雾化尼古丁的可行性。
成年雌性和雄性 C57BL/6 小鼠被训练辨别 0.75mg/kg 皮下(s.c.)尼古丁与盐水。在确定 s.c.尼古丁剂量效应曲线后,评估了雾化游离碱尼古丁和含有尼古丁的烟草产品(即,无口味和北极冲击波电子烟液)。
尼古丁(s.c.)剂量依赖性地替代了雌雄小鼠,尽管雌性表现出较低的敏感性和较大的变异性。相比之下,无论配方如何,雾化尼古丁都会产生浓度依赖性增加,最高可达 46-62%的尼古丁相关反应。对于每个性别,s.c.0.75mg/kg 尼古丁和 30mg/ml 游离碱尼古丁的脑尼古丁浓度相似。
雌雄小鼠都容易获得 s.c.尼古丁辨别,但雌性表现出较低的敏感性。此外,雾化尼古丁的所有三种配方都在雌雄小鼠中产生了尼古丁样反应的增加。然而,这些增加的最大幅度并没有产生与 s.c.0.75mg/kg 尼古丁相似的替代程度,尽管 30mg/ml 雾化尼古丁的脑尼古丁浓度相似。需要进一步研究以确定原因;然而,这里的结果表明,对于检查雾化药物(如尼古丁)的辨别刺激效应的初步可行性。