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评估可燃香烟吸食者对电子烟的滥用倾向。

Abuse liability assessment of an electronic cigarette in combustible cigarette smokers.

机构信息

Department of Psychology, College of Humanities and Sciences, Virginia Commonwealth University.

Department of Internal Medicine, Division of General Internal Medicine, Virginia Commonwealth University.

出版信息

Exp Clin Psychopharmacol. 2019 Oct;27(5):443-454. doi: 10.1037/pha0000261. Epub 2019 Feb 18.

Abstract

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).

摘要

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)。

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