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对乙酰氨基酚在人体内的消除半衰期不受短期无硫氨基酸饮食的影响。

Acetaminophen elimination half-life in humans is unaffected by short-term consumption of sulfur amino acid-free diet.

机构信息

Graduate Program in Molecular and Systems Pharmacology, Emory University, Atlanta, Georgia 30322, USA.

出版信息

J Pharmacol Exp Ther. 2010 Jun;333(3):948-53. doi: 10.1124/jpet.110.166439. Epub 2010 Mar 5.

Abstract

Sulfation and glutathione (GSH) conjugation are important pathways for elimination of acetaminophen (APAP). Previous studies in rodents show that limitation of dietary sulfur amino acids (SAAs) reduces biosynthesis of 3'-phosphoadenosine-5'-phosphosulfate, the precursor for sulfation, and GSH, the precursor for the mercapturatic acid pathway. The amount of SAA needed for the metabolism of two doses of APAP is equivalent to 62% of the recommended dietary allowance (RDA) for SAA in humans. A decrease in the activity of these metabolic pathways could lead to decreased elimination of the reactive metabolite of APAP and possibly affect risk of APAP use. To determine whether intake of a SAA-deficient diet alters APAP metabolism, a pilot clinical study with a double-blind, cross-over design was performed. Subjects received the RDA for SAA for 3 days for equilibration. After admission to the clinical research unit, subjects were given a chemically defined diet with 100 or 0% of the RDA for SAA for 2 days. On day 3, two doses of APAP (15 mg/kg) or placebo were given successively within a 6-h interval. Plasma samples were collected at baseline and hourly for 12 h, and two 6-h urine aliquots were collected during this time course. The data show that SAA limitation 1) did not change the pattern of APAP metabolites in plasma or urine and 2) did not alter APAP pharmacokinetics. Thus, the results show that 2 days of diet completely devoid of SAA have no effect on APAP metabolism or disposition in healthy humans.

摘要

磺化和谷胱甘肽(GSH)缀合是消除对乙酰氨基酚(APAP)的重要途径。 以前在啮齿动物中的研究表明,限制饮食中的含硫氨基酸(SAA)会减少磺酸盐的前体 3'-磷酸腺苷-5'-磷酸硫酸和 GSH 的生物合成,GSH 是巯基尿酸途径的前体。 代谢两剂 APAP 所需的 SAA 量相当于人类 SAA 推荐膳食允许量(RDA)的 62%。 这些代谢途径的活性降低可能导致 APAP 反应性代谢物的消除减少,并可能影响 APAP 使用的风险。 为了确定 SAA 缺乏饮食是否会改变 APAP 的代谢,进行了一项双盲,交叉设计的初步临床研究。 受试者接受 SAA 的 RDA 平衡 3 天。 进入临床研究单位后,受试者接受了一种化学定义的饮食,其中 SAA 的 RDA 为 100%或 0%,持续 2 天。 在第 3 天,在 6 小时的间隔内先后给予受试者两剂 APAP(15mg/kg)或安慰剂。 在基线和 12 小时内每小时收集血浆样本,并在此时间过程中收集两个 6 小时尿液等分试样。 数据显示,SAA 限制 1)没有改变血浆或尿液中 APAP 代谢物的模式,2)没有改变 APAP 的药代动力学。 因此,结果表明,2 天完全缺乏 SAA 的饮食对健康人体中的 APAP 代谢或处置没有影响。

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