Department of Psychology, College of Humanities and Sciences, Virginia Commonwealth University.
Department of Internal Medicine, Division of General Internal Medicine, Virginia Commonwealth University.
Exp Clin Psychopharmacol. 2019 Oct;27(5):443-454. doi: 10.1037/pha0000261. Epub 2019 Feb 18.
Under certain conditions, electronic cigarettes (e-cigs) can deliver nicotine to and suppress tobacco abstinence symptoms in cigarette smokers. Growing popularity of e-cigs raises abuse liability concerns. This study's purpose was to compare the abuse liability of an e-cig (1.5 Ohm, 3.3 V) filled with 36 mg/mL or 0 mg/mL nicotine to an Food and Drug Administration (FDA)-approved nicotine inhaler (IN) and participants' own brand (OB) of cigarettes. Smokers (N = 24) completed four sessions in which they completed the multiple-choice procedure, and plasma nicotine concentration and subjective effects were measured. Mean (SD) multiple-choice procedure crossover point was $0.87 (1.0) for the 36-mg/mL nicotine e-cig and $0.96 (1.2) for the 0-mg/mL e-cig, significantly higher than the IN mean of $0.32 (0.6) but significantly lower than the OB cigarette mean of $1.42 (1.4). Ten puffs from an own-brand cigarette increased mean plasma nicotine concentration from 3.55 (2.8) to 13.64 (9.8) ng/mL, as compared to an increase from 3.16 (1.8) to 8.51 (5.4) ng/mL for the 36-mg/mL e-cig. The 36-mg/mL e-cig reduced nicotine abstinence symptoms more than the 0-mg/mL e-cig, and both e-cigs were rated as more reinforcing than the inhaler but less reinforcing than participants' OB cigarettes (ps < .05). Results suggest that the e-cig examined had higher abuse liability than the IN but lower than combustible cigarettes. These data and methods may be useful for policymakers by revealing how e-cig abuse liability compares to tobacco/nicotine products with abuse liability profiles that are well established. (PsycINFO Database Record (c) 2019 APA, all rights reserved).
在某些条件下,电子烟(e-cigs)可以向吸烟者输送尼古丁并抑制其戒烟症状。电子烟日益普及,引发了滥用风险的担忧。本研究旨在比较 1.5 欧姆、3.3 伏特的 36 毫克/毫升尼古丁电子烟与食品和药物管理局(FDA)批准的尼古丁吸入器(IN)和参与者自身品牌(OB)香烟的滥用风险。吸烟者(N=24)完成了四个阶段的实验,他们完成了多项选择程序,并测量了血浆尼古丁浓度和主观效果。36 毫克/毫升尼古丁电子烟的平均(SD)多项选择程序交叉点为 0.87(1.0),0 毫克/毫升电子烟的交叉点为 0.96(1.2),显著高于 IN 的 0.32(0.6),但显著低于 OB 香烟的 1.42(1.4)。与使用 36 毫克/毫升电子烟相比,抽完自身品牌的一支香烟后,血浆尼古丁浓度从 3.55(2.8)增加到 13.64(9.8)ng/mL,增加了 10.09(9.8)ng/mL;而从 3.16(1.8)增加到 8.51(5.4)ng/mL。36 毫克/毫升电子烟比 0 毫克/毫升电子烟能更有效地减轻尼古丁戒断症状,与吸入器相比,两者都被评为更具强化作用,但比参与者的 OB 香烟的强化作用弱(p<.05)。结果表明,研究中使用的电子烟的滥用风险高于 IN,但低于可燃香烟。这些数据和方法可能对政策制定者有用,因为它们揭示了电子烟的滥用风险与滥用风险特征明确的烟草/尼古丁产品相比如何。(PsycINFO 数据库记录(c)2019 APA,保留所有权利)。