Levitt M D, Levitt D G
Research Service, Veterans Affairs Medical Center, Minneapolis, Minnesota.
J Pharmacol Exp Ther. 1994 Apr;269(1):297-304.
The area under blood ethanol concentration-time curves may be lower after ingestion vs. intravenous infusion of similar ethanol doses, a difference that has been attributed to first-pass metabolism in the gastric mucosa. Using a model of human hepatic ethanol metabolism, we predicted the area under blood ethanol concentration-time curves and first-pass metabolism that would result from oral vs. intravenous ethanol. This model accurately predicted reported differences in AUC after oral vs. intravenous ethanol. First-pass metabolism has been shown to disappear when the stomach is bypassed via intraduodenal or portal vein infusion of ethanol. Our model predicts that the efficiency of first-pass metabolism is extremely sensitive to the hepatic delivery rate of ethanol and the rapid ethanol delivery rate in bypass studies would have eliminated hepatic first-pass metabolism. We conclude that hepatic ethanol metabolism could explain published observations concerning first-pass metabolism and it is not necessary to postulate a major role for gastric mucosal metabolism in this process. Inhibition of the liver's ability to oxidize ethanol is a necessary requirement of any theory proposing that the gastric mucosa is the primary site of first-pass ethanol metabolism.
摄入相同剂量乙醇后,血乙醇浓度-时间曲线下面积可能低于静脉输注,这种差异归因于胃黏膜的首过代谢。使用人类肝脏乙醇代谢模型,我们预测了口服与静脉注射乙醇后血乙醇浓度-时间曲线下面积及首过代谢情况。该模型准确预测了口服与静脉注射乙醇后报道的曲线下面积差异。当通过十二指肠内或门静脉输注乙醇绕过胃部时,首过代谢已被证明会消失。我们的模型预测,首过代谢效率对乙醇的肝脏输送速率极为敏感,而在绕过研究中快速的乙醇输送速率会消除肝脏首过代谢。我们得出结论,肝脏乙醇代谢可以解释已发表的关于首过代谢的观察结果,在此过程中没有必要假定胃黏膜代谢起主要作用。抑制肝脏氧化乙醇的能力是任何提出胃黏膜是首过乙醇代谢主要部位理论的必要条件。