Cusack B J, Dawson G W, Mercer G D, Vestal R E
Clin Pharmacol Ther. 1985 Mar;37(3):330-6. doi: 10.1038/clpt.1985.48.
The inhibition of theophylline metabolism by cimetidine was investigated in young male cigarette smokers (greater than 20 cigarettes/day) and nonsmokers by stable isotope methodology. Subjects received oral theophylline (510 mg/day) for 14 days and cimetidine (1200 mg/day) over days 1 to 7 or 8 to 14. On days 7 and 14, a tracer dose (10 mg) of stable isotope-labeled theophylline was injected intravenously with the oral dose of theophylline. Serial plasma samples were then obtained for 24 hours and both molecular forms of theophylline were assayed by mass spectrometry after purification by HPLC. Theophylline bioavailability, volume of distribution, and protein binding were of the same order in both groups and were not affected by cimetidine. Although the basal theophylline elimination rate constant was 46% greater and clearance was 54% greater in smokers than in nonsmokers, the proportionate changes in steady-state plasma concentrations, t1/2, and clearance due to cimetidine were much the same in both groups. Plasma thiocyanate concentrations were higher in smokers than in nonsmokers and were related to theophylline clearance. Our findings indicate that cimetidine inhibits theophylline metabolism to a similar extent in both smokers and nonsmokers. Determination of plasma thiocyanate levels may be valuable in the prediction of theophylline clearance.
采用稳定同位素方法,在年轻男性吸烟者(每天吸烟超过20支)和非吸烟者中研究了西咪替丁对茶碱代谢的抑制作用。受试者口服茶碱(510毫克/天),持续14天,在第1至7天或第8至14天服用西咪替丁(1200毫克/天)。在第7天和第14天,静脉注射示踪剂量(10毫克)的稳定同位素标记茶碱,并同时口服茶碱。随后连续24小时采集血浆样本,通过高效液相色谱法纯化后,用质谱法测定茶碱的两种分子形式。两组的茶碱生物利用度、分布容积和蛋白结合情况处于同一水平,且不受西咪替丁影响。虽然吸烟者的基础茶碱消除速率常数比非吸烟者高46%,清除率高54%,但两组中由于西咪替丁导致的稳态血浆浓度、半衰期和清除率的相应变化大致相同。吸烟者的血浆硫氰酸盐浓度高于非吸烟者,且与茶碱清除率相关。我们的研究结果表明,西咪替丁在吸烟者和非吸烟者中对茶碱代谢的抑制程度相似。测定血浆硫氰酸盐水平可能对预测茶碱清除率有价值。