Rose J Q, Yurchak A M, Meikle A W, Jusko W J
J Pharmacokinet Biopharm. 1981 Feb;9(1):1-14. doi: 10.1007/BF01059339.
The pharmacokinetics of oral prednisone and oral dexamethasone were examined in 18 healthy male adults. Eight subjects also received intravenous prednisolone and intravenous dexamethasone. Half of each group were cigarette smokers as confirmed by plasma thiocyanate concentrations. Plasma and urine concentrations of prednisone and prednisolone were assayed by high performance liquid chromatography, while plasma dexamethasone was measured by radioimmunoassay. There were no statistically significant differences between smokers and nonsmokers in the systemic availability of prednisolone (75 versus 84%), oral dose clearance of prednisone (29 verus 27 ml/min/kg), systemic prednisolone clearance (2.8 versus 2.9 ml/min/kg), or in the interconversion rates, volumes of distribution, or urinary recoveries of prednisone and prednisolone. Similarly, the pharmacokinetics of dexamethasone were unaffected by smoking. A limited correlation (r = 0.55) was found between the high oral dose clearances of prednisone and the lower values of dexamethasone (6.73 and 5.71 ml/min/kg in smokers and nonsmokers). A two- to threefold variability occurred in oral dose clearances of each steroid with partial intrasubject covariance. Unlike the anticonvulsants, which markedly induce corticosteroid metabolism, smoking has no effect on their pharmacokinetics and should not complicate therapy with these drugs.
在18名健康成年男性中研究了口服泼尼松和口服地塞米松的药代动力学。8名受试者还接受了静脉注射泼尼松龙和静脉注射地塞米松。根据血浆硫氰酸盐浓度确认,每组中有一半是吸烟者。泼尼松和泼尼松龙的血浆及尿液浓度通过高效液相色谱法测定,而血浆地塞米松则通过放射免疫分析法测定。吸烟者和不吸烟者在泼尼松龙的全身可用性(75%对84%)、泼尼松的口服剂量清除率(29对27 ml/min/kg)、全身泼尼松龙清除率(2.8对2.9 ml/min/kg)方面,或在泼尼松和泼尼松龙的相互转化率、分布容积或尿回收率方面,均无统计学显著差异。同样,吸烟对地塞米松的药代动力学没有影响。在泼尼松的高口服剂量清除率与地塞米松的较低值(吸烟者和不吸烟者分别为6.73和5.71 ml/min/kg)之间发现了有限的相关性(r = 0.55)。每种类固醇的口服剂量清除率存在两到三倍的变异性,且有部分个体内协方差。与明显诱导皮质类固醇代谢的抗惊厥药不同,吸烟对其药代动力学没有影响,也不应使这些药物的治疗复杂化。