Fountaine Robert, Milton Ashley, Checchio Tina, Wei Greg, Stolar Marilyn, Teeter John, Jaeger Rudolph, Fryburg David
Pfizer Global Research and Development, Groton, CT and Environmental Medicine Incorporated, Westwood, NJ, USA.
Br J Clin Pharmacol. 2008 Jun;65(6):864-70. doi: 10.1111/j.1365-2125.2008.03122.x.
Active cigarette smoking is associated with increased permeability of the pulmonary alveolar epithelium, resulting in faster absorption of inhaled drugs such as Exubera (EXU). Absorption of EXU is increased approximately twice to four times as much in chronic smokers compared with nonsmokers. The rate of clearance of radioaerosols such as technetium-labelled diethylenetriamine penta-acetic acid is decreased in response to passive smoke exposure.
Passive smoke exposure causes a decrease in lung permeability, an effect opposite to that of active smoking. Acute passive smoke exposure results in a decrease in EXU bioavailability and does not create a risk of hypoglycaemia. These results are consistent with previous studies of radioaerosol lung clearance. AIMS Relative to nonsmokers, the bioavailability of inhaled human insulin (Exubera(R); EXU) is markedly increased in chronic smokers. The pharmacokinetics of EXU following passive cigarette smoke exposure is unknown. METHODS In an open-label, crossover study, healthy nonsmoking volunteers received two treatments in randomized sequence separated by a 2-week wash-out: (i) EXU 3 mg with no passive smoke exposure and (ii) EXU 3 mg after passive smoke exposure (atmospheric nicotine levels 75-125 mug m(-3)) for 2 h. Blood samples were obtained at prespecified times up to 6 h after EXU administration.
Twenty-seven subjects completed both study periods. Mean plasma insulin AUC(0-360) decreased by 17% [ratio 83%, 95% confidence interval (CI) 68.8, 99.5] and mean C(max) by 29% (ratio 71%, 95% CI 59.8, 83.1) after passive cigarette smoke exposure. The median (range) t(max) was 60 min (20-120 min) and 75 min (20-360 min) in the EXU with no exposure and EXU passive exposure groups, respectively. EXU was well tolerated.
Unlike active chronic smoking, acute passive cigarette smoke exposure modestly decreases EXU bioavailability and thus should not increase hypoglycaemia risk. These results are consistent with those from published literature involving technetium-labelled diethylenetriamine penta-acetic acid and suggest that passive cigarette smoke exposure causes an acute decrease in lung permeability vs. active smoking, which causes an increase in permeability.
主动吸烟与肺泡上皮通透性增加有关,导致吸入药物(如依克那肽(EXU))的吸收加快。与非吸烟者相比,慢性吸烟者中依克那肽的吸收增加约两倍至四倍。接触二手烟会导致放射性气溶胶(如锝标记的二乙三胺五乙酸)的清除率降低。
接触二手烟会导致肺通透性降低,这一效应与主动吸烟相反。急性接触二手烟会导致依克那肽的生物利用度降低,且不会产生低血糖风险。这些结果与先前关于放射性气溶胶肺清除率的研究一致。目的相对于非吸烟者,慢性吸烟者中吸入人胰岛素(依克那肽(Exubera®;EXU))的生物利用度显著增加。接触二手烟后依克那肽的药代动力学尚不清楚。方法在一项开放标签、交叉研究中,健康的非吸烟志愿者按随机顺序接受两种治疗,间隔2周洗脱期:(i)吸入3毫克依克那肽且无二手烟接触,(ii)吸入3毫克依克那肽后接触二手烟(大气尼古丁水平75 - 125微克/立方米)2小时。在给予依克那肽后长达6小时的预定时间采集血样。
27名受试者完成了两个研究阶段。接触二手烟后,血浆胰岛素平均AUC(0 - 360)降低了17%[比值83%,95%置信区间(CI)68.8,99.5],平均C(max)降低了29%(比值71%,95%CI 59.8,83.1)。在无接触依克那肽组和接触二手烟依克那肽组中,t(max)的中位数(范围)分别为60分钟(20 - 120分钟)和75分钟(20 - 360分钟)。依克那肽耐受性良好。
与慢性主动吸烟不同,急性接触二手烟会适度降低依克那肽的生物利用度,因此不应增加低血糖风险。这些结果与已发表的涉及锝标记的二乙三胺五乙酸的文献结果一致,表明接触二手烟会导致肺通透性急性降低,而主动吸烟会导致通透性增加。