Jones Alan Wayne, Lindberg Lars, Olsson Sven-Gunnar
Department of Forensic Toxicology, University Hospital, Linköping, Sweden.
Clin Pharmacokinet. 2004;43(15):1157-66. doi: 10.2165/00003088-200443150-00006.
Human studies of arterio-venous (AV) differences in drug concentrations and the consequences for pharmacokinetic modelling and concentration-effect relationships are very limited. We therefore investigated the intravenous and intra-arterial concentrations of alcohol (ethanol) during the absorption, distribution and elimination stages of alcohol metabolism in healthy men.
Nine male volunteers aged 26-67 years drank 0.6 g alcohol/kg bodyweight in 2-15 minutes. The drink was prepared from 95% v/v alcohol, which was diluted with an alcohol-free beverage to 20% v/v. Before the start of drinking and for 6-7 hours post-administration, blood samples were drawn at 15- to 20-minute intervals from indwelling catheters in a radial artery and a cubital vein on the same arm. The blood-alcohol concentration (BAC) was determined by headspace gas chromatography, and blood-water content was measured by desiccation.
The peak concentration (Cmax) of alcohol in arterial blood was 0.98 g/L (SD 0.209) compared with 0.84 g/L (SD 0.176) for venous blood (p < 0.001), whereas median time to reach Cmax (tmax) was the same (35 minutes). The AV difference was greatest at 10 minutes after the end of drinking (mean 0.20 g/L [range 0.09-0.40 g/L]), decreasing as the absorption of alcohol continued. At a median time of 90 minutes post-administration (range 45-105 minutes), the AV difference was momentarily zero. At later times, the AV differences became increasingly negative and at 280 minutes post-administration the mean was -0.051 g/L (range -0.025 to -0.078 g/L). The slope of the post-absorptive phase (k0) was 0.116 g/L/h (SD 0.0167) for arterial blood compared with 0.109 g/L/h (SD 0.0185) for venous blood (p < 0.001). The extrapolated time to reach zero BAC was 391 minutes (SD 34) for arterial blood and 420 minutes (SD 41) for venous blood; the difference of 29 minutes was statistically highly significant (p < 0.001). The apparent volume of distribution of alcohol, the area under the concentration-time curves (AUC) and the water content of arterial and venous blood samples were not significantly different for the two sampling compartments.
The arterial and venous blood-alcohol profiles were shifted in time owing to the time it takes for alcohol to equilibrate between arterial blood and tissue water. Alcohol is metabolised in the liver but not in muscle tissue, which acts as a reservoir for alcohol. The concentrations of alcohol in arterial and venous blood were the same at only one timepoint, which signifies complete equilibration of alcohol in total body water. During the entire post-absorptive phase, the concentration of alcohol in venous blood draining skeletal muscles was slightly greater than the arterial blood concentration; therefore, the AV differences were negative.
关于动静脉药物浓度差异以及对药代动力学建模和浓度-效应关系影响的人体研究非常有限。因此,我们研究了健康男性在酒精代谢的吸收、分布和消除阶段静脉和动脉内酒精(乙醇)的浓度。
9名年龄在26至67岁的男性志愿者在2至15分钟内饮用了0.6克酒精/千克体重。饮料由95%(v/v)酒精配制而成,并用无酒精饮料稀释至20%(v/v)。在饮酒开始前以及给药后6至7小时内,每隔15至20分钟从同一手臂的桡动脉和肘静脉内留置导管采集血样。采用顶空气相色谱法测定血液酒精浓度(BAC),通过干燥法测量血液含水量。
动脉血中酒精的峰值浓度(Cmax)为0.98克/升(标准差0.209),而静脉血为0.84克/升(标准差0.176)(p < 0.001),然而达到Cmax的中位时间(tmax)相同(35分钟)。饮酒结束后10分钟时动静脉差异最大(平均0.20克/升[范围0.09 - 0.40克/升]),随着酒精吸收的持续而减小。给药后中位时间90分钟(范围45 - 105分钟)时,动静脉差异瞬间为零。在之后的时间里,动静脉差异变得越来越负,给药后280分钟时平均值为 -0.051克/升(范围 -0.025至 -0.078克/升)。吸收后阶段的斜率(k0),动脉血为0.116克/升/小时(标准差0.0167),静脉血为0.109克/升/小时(标准差0.0185)(p < 0.001)。动脉血达到零BAC的外推时间为391分钟(标准差34),静脉血为420分钟(标准差41);29分钟的差异具有高度统计学意义(p < 0.001)。两个采样部位酒精的表观分布容积、浓度-时间曲线下面积(AUC)以及动脉和静脉血样的含水量无显著差异。
由于酒精在动脉血和组织水之间达到平衡所需的时间,动脉和静脉血液酒精曲线在时间上发生了偏移。酒精在肝脏中代谢,但不在肌肉组织中代谢,肌肉组织起到酒精储存库的作用。动脉血和静脉血中酒精浓度仅在一个时间点相同,这表明酒精在全身水中完全平衡。在整个吸收后阶段,引流骨骼肌的静脉血中酒精浓度略高于动脉血浓度;因此,动静脉差异为负。