Elvin A T, Cole A F, Pieper J A, Rolbin S H, Lalka D
Clin Pharmacol Ther. 1981 Oct;30(4):455-60. doi: 10.1038/clpt.1981.188.
The effect of high-protein meal on the hepatic clearance (ClH) of intravenous lidocaine, because of its conceptual importance in understanding first-pass metabolic phenomena, was evaluated in nine healthy males. Our randomized crossover study demonstrated that mean ClH rose from 1245 to 1477 ml/min (P less than 0.03) as a result of the meal (i.e., mean area under the blood concentration-time curve decreased 20%). The magnitude of the change in clearance correlated weakly with fasting ClH (r = 0.54; slope = -0.037% per ml/min; intercept = 67.2%; P less than 0.15). In a separate study, it was observed that the meal did not influence lidocaine serum protein binding; the free fraction of lidocaine in samples drawn from the subjects in the fasting state averaged 0.305 +/- 0.027 while that from subjects who had eaten was 0.321 +/- 0.042. These data suggest that the mean clearance of lidocaine is increased by stimulation of hepatic blood flow rate. Furthermore, the magnitude of this increase is consistent with expectations based on a simple physiologic model. Thus, these data provide experimental support for the hypothesis that transient increases in splanchnic blood flow rate observed after a high-protein meal may explain apparent improvement of the oral bioavailability of model high intrinsic clearance drugs.
由于高蛋白餐对静脉注射利多卡因肝脏清除率(ClH)的影响在理解首过代谢现象方面具有重要的概念意义,因此在9名健康男性中进行了评估。我们的随机交叉研究表明,由于进食,平均ClH从1245 ml/min升至1477 ml/min(P<0.03)(即血药浓度-时间曲线下平均面积下降20%)。清除率变化的幅度与空腹ClH弱相关(r = 0.54;斜率=-0.037%/ml/min;截距=67.2%;P<0.15)。在另一项研究中,观察到进食不影响利多卡因的血清蛋白结合;空腹状态下受试者样本中利多卡因的游离分数平均为0.305±0.027,而进食后受试者的游离分数为0.321±0.042。这些数据表明,利多卡因的平均清除率因肝血流速率的刺激而增加。此外,这种增加的幅度与基于简单生理模型的预期一致。因此,这些数据为以下假设提供了实验支持:高蛋白餐后观察到的内脏血流速率的短暂增加可能解释了模型高内在清除率药物口服生物利用度的明显改善。