Department of Family Medicine and Community Health, University of Minnesota Medical School, Minneapolis, MN 55414, USA.
Nicotine Tob Res. 2012 Jun;14(6):688-93. doi: 10.1093/ntr/ntr268. Epub 2012 Feb 8.
Despite the widespread use of mentholated cigarettes, lower cessation rates, and disproportionately high smoking-related morbidity among Blacks, the possible role of menthol in smokers' response to pharmacotherapy has not been well-studied. This study examined the effects of menthol on the pharmacokinetic (PK) profiles of bupropion and its principal metabolites, hydroxybupropion, threohydrobupropion, and erythrohydrobupropion among Black smokers.
After a 7-day placebo run-in period, participants received 150 mg bid sustained-release bupropion for 20-25 days. Blood samples were drawn for PK analysis on 2 occasions, 10-15 days after the commencement of bupropion while participants were still smoking (smoking phase) and at days 20-25 when they were asked not to smoke (nonsmoking phase).
18 smokers of nonmenthol cigarettes and 23 smokers of menthol cigarettes were enrolled in this study. No differences were found by menthol smoking status in the Cmax and area under the plasma concentration versus time curve (AUC) of bupropion and its metabolites in the smoking or nonsmoking phases. However, among menthol smokers, the AUC ratios of metabolite/bupropion were lower in the nonsmoking phase compared with the smoking phase (hydro/bup = 31.49 ± 18.84 vs. 22.95 ± 13.27, p = .04; erythro/bup = 1.99 ± 1.02 vs. 1.76 ± 0.75, p = .016; threo/bup = 11.77 ± 8.90 vs. 10.44 ± 5.63, p = .034). No significant differences were found in the metabolite/bup ratios between smoking and nonsmoking conditions among nonmenthol smokers.
We did not find a significant effect of menthol compared with nonmenthol cigarette smoking on the PKs of bupropion and metabolites at steady state. More research is needed to advance the understanding of mechanisms underlying disparities in smoking cessation outcomes related to smoking of menthol cigarettes.
尽管薄荷醇香烟的使用广泛,但黑人的戒烟率较低,与吸烟有关的发病率较高,但薄荷醇在吸烟者对药物治疗反应中的可能作用尚未得到充分研究。本研究检查了薄荷醇对黑人吸烟者中丁丙诺啡的药代动力学(PK)谱的羟丁丙诺啡、苏羟丁丙诺啡、赤羟丁丙诺啡和赤羟丁丙诺啡的影响。
在 7 天的安慰剂导入期后,参与者接受了 150mg bid 缓释丁丙诺啡,持续 20-25 天。在开始使用丁丙诺啡后 10-15 天(吸烟期)和第 20-25 天(非吸烟期),当参与者被要求不吸烟时,抽取两次血样进行 PK 分析。
这项研究共纳入了 18 名吸非薄荷醇香烟的吸烟者和 23 名吸薄荷醇香烟的吸烟者。在吸烟或不吸烟阶段,薄荷醇吸烟状态与丁丙诺啡及其代谢物的 Cmax 和血浆浓度-时间曲线下面积(AUC)无差异。然而,在薄荷醇吸烟者中,与吸烟期相比,非吸烟期代谢物/丁丙诺啡的 AUC 比值较低(羟丁丙诺啡=31.49±18.84 vs. 22.95±13.27,p=0.04;赤羟丁丙诺啡=1.99±1.02 vs. 1.76±0.75,p=0.016;苏羟丁丙诺啡=11.77±8.90 vs. 10.44±5.63,p=0.034)。在非薄荷醇吸烟者中,吸烟和不吸烟条件下的代谢物/丁丙诺啡比值无显著差异。
与吸非薄荷醇香烟相比,我们没有发现薄荷醇对丁丙诺啡及其代谢物在稳态时的 PKs 有显著影响。需要进一步研究以深入了解与吸薄荷醇香烟有关的戒烟结果差异的机制。