Breland A B, Evans S E, Buchhalter A R, Eissenberg T
Department of Psychology and Institute for Drug and Alcohol Studies, Virginia Commonwealth University, Richmond, Virginia 23298-0205, USA.
Tob Control. 2002 Dec;11(4):376-8. doi: 10.1136/tc.11.4.376.
To examine the acute effects of Advance, a potential reduced exposure product (PREP) for smokers marketed as a means to reduce exposure to toxic gases and tobacco specific nitrosamines.
DESIGN, SETTING, PARTICIPANTS: Latin square ordered, three condition, laboratory based, crossover design with 20 smokers of light or ultra-light cigarettes (15 or more cigarettes/day). In each 2.5 hour condition, participants completed an 8-puff smoking bout from their own brand, Advance, or an unlit cigarette (that is, sham smoking) every 30 minutes for a total of four bouts.
Subject rated measures of tobacco/nicotine withdrawal; carbon monoxide (CO), and heart rate; plasma nicotine concentrations.
Relative to own brand, Advance produced similar withdrawal suppression and heart rate increase, lower CO boost, and higher plasma nicotine concentrations.
PREPs for smokers need to be evaluated using a comprehensive strategy that includes empirical examination of acute and long term effects. Adequate withdrawal suppression and potentially lower concentrations of CO associated with Advance use are positive factors, although higher nicotine concentrations do not constitute "reduced exposure". Overall, longer exposure periods are necessary to determine carcinogen delivery. PREP evaluation is complex and should be completed objectively.
研究Advance(一种面向吸烟者的潜在低暴露产品,宣传可减少有毒气体和烟草特有亚硝胺暴露)的急性效应。
设计、地点、参与者:拉丁方序、三条件、基于实验室的交叉设计,纳入20名吸淡味或超淡味香烟(每天15支或更多)的吸烟者。在每个2.5小时的条件下,参与者每30分钟从自己的品牌香烟、Advance或未点燃的香烟(即假吸烟)中进行一次8口吸烟,共进行四轮。
受试者对烟草/尼古丁戒断、一氧化碳(CO)和心率的评分;血浆尼古丁浓度。
相对于自己的品牌香烟,Advance产生了相似的戒断抑制和心率升高,较低的CO增加量,以及较高的血浆尼古丁浓度。
需要采用综合策略评估吸烟者的低暴露产品,该策略包括对急性和长期效应的实证研究。Advance使用时充分的戒断抑制以及可能较低的CO浓度是积极因素,尽管较高的尼古丁浓度并不构成“低暴露”。总体而言,需要更长的暴露时间来确定致癌物的释放量。低暴露产品评估很复杂,应客观完成。