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乙醇浓度-时间曲线的个体间和个体内变异性:晚餐前后乙醇摄入量的比较。

Inter-individual and intra-individual variability of ethanol concentration-time profiles: comparison of ethanol ingestion before or after an evening meal.

作者信息

Fraser A G, Rosalki S B, Gamble G D, Pounder R E

机构信息

University Department of Medicine, Royal Free Hospital School of Medicine, London, UK.

出版信息

Br J Clin Pharmacol. 1995 Oct;40(4):387-92. doi: 10.1111/j.1365-2125.1995.tb04561.x.

DOI:10.1111/j.1365-2125.1995.tb04561.x
PMID:8554941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1365158/
Abstract
  1. The magnitude of the variability of ethanol absorption is an important factor for studies that seek to determine the significance of potential interactions between ethanol and drugs. The aim of this study was to determine the extent of inter- and intra-individual variability of ethanol concentration-time profiles in fasted and fed subjects. 2. Twenty-four healthy male subjects were randomized to receive ethanol 0.3 g kg-1 before an evening meal on two study days and ethanol 0.3 g kg-1 after an evening meal on two study days. Plasma ethanol concentrations were measured at intervals from 0-240 min. 3. There were significant differences in the mean area under the ethanol concentration-time curve (AUC), the mean peak ethanol concentration (Cmax), the mean ethanol elimination slope and the time to peak ethanol concentration between the fed and fasted subjects. There were no significant differences between the first and second study days for either fed or fasting subjects for all parameters. 4. There was no statistically significant difference in inter- or intra-subject variance between fed and fasted studies although the coefficients of variation (standard deviation expressed as a percentage of the mean) for the differences between the first and second study day were higher for fed studies. 5. The large inter- and intra-individual variability of alcohol absorption for both fasted and fed subjects must be considered in the design of alcohol-drug interaction studies.
摘要
  1. 乙醇吸收变异性的大小是那些试图确定乙醇与药物之间潜在相互作用重要性的研究中的一个重要因素。本研究的目的是确定禁食和进食受试者中乙醇浓度-时间曲线的个体间和个体内变异性程度。2. 24名健康男性受试者被随机分为两组,在两个研究日的晚餐前接受0.3 g/kg的乙醇,在另外两个研究日的晚餐后接受0.3 g/kg的乙醇。在0至240分钟内定期测量血浆乙醇浓度。3. 进食和禁食受试者之间在乙醇浓度-时间曲线下的平均面积(AUC)、平均乙醇峰值浓度(Cmax)、平均乙醇消除斜率以及乙醇达到峰值浓度的时间方面存在显著差异。对于进食或禁食受试者,所有参数在第一个和第二个研究日之间均无显著差异。4. 进食和禁食研究之间的受试者间或受试者内方差没有统计学上的显著差异,尽管进食研究中第一个和第二个研究日之间差异的变异系数(标准差表示为平均值的百分比)更高。5. 在酒精-药物相互作用研究的设计中,必须考虑禁食和进食受试者酒精吸收的个体间和个体内的巨大变异性。

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本文引用的文献

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An enzymatic method for the microdetermination of ethanol.一种微量测定乙醇的酶法。
Scand J Clin Lab Invest. 1951;3(1):58-62. doi: 10.3109/00365515109060572.
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Effects of erythromycin on gastric emptying, alcohol absorption and small intestinal transit in normal subjects.红霉素对正常受试者胃排空、酒精吸收及小肠转运的影响。
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Ranitidine has no effect on postbreakfast ethanol absorption.雷尼替丁对早餐后乙醇吸收没有影响。
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Absence of effect of ranitidine on blood alcohol concentrations when taken morning, midday, or evening with or without food.
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Review article: lack of clinical significance of the interaction between H2-receptor antagonists and ethanol.综述文章:H2受体拮抗剂与乙醇相互作用缺乏临床意义
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Can the liver account for first-pass metabolism of ethanol in the rat?肝脏能否解释大鼠体内乙醇的首过代谢?
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Alcohol absorption, gastric emptying and a breathalyser.酒精吸收、胃排空与呼气测醉器
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