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单次及重复给予双硫仑后,人红细胞醛脱氢酶活性的抑制以及二乙基二硫代氨基甲酸甲酯及其单硫类似物的消除动力学

Inhibition of erythrocyte aldehyde dehydrogenase activity and elimination kinetics of diethyldithiocarbamic acid methyl ester and its monothio analogue after administration of single and repeated doses of disulfiram to man.

作者信息

Johansson B, Stankiewicz Z

机构信息

Department of Clinical Chemistry, General Hospital, Malmö, Sweden.

出版信息

Eur J Clin Pharmacol. 1989;37(2):133-8. doi: 10.1007/BF00558220.

Abstract

The elimination kinetics of the methyl esters of diethyldithiocarbamic acid (Me-DDC) and its monothio analogue (Me-DTC) has been compared in ten alcoholic patients after a single oral dose of 400 mg disulfiram (Antabuse). Erythrocyte aldehyde dehydrogenase (ALDH) activity was continuously followed in the subjects until complete inactivation. The relation between individual steady-state concentrations of Me-DTC in plasma, blood acetaldehyde concentration and the dose of disulfiram sufficient to give the disulfiram alcohol reaction was investigated in 12 healthy volunteers treated with increasing doses of disulfiram and then challenged with ethanol. The mean peak plasma concentration of Me-DDC occurred at 1.8 h and its plasma half-life was 6.3 h. The corresponding values for Me-DTC were 3.3 h and 11.2 h, respectively. This suggests oxidative formation of Me-DTC from Me-DDC. In alcoholics with a rapid decrease in erythrocyte ALDH activity (in less than 5 days), the mean peak plasma concentration of Me-DTC was 278 nmol.l-1, whereas the peak concentration was below the detection limit in subjects with a prolonged inactivation time (7-20 days). The healthy volunteers were divided into three groups of four subjects, with clinically valid disulfiram alcohol reactions at 100, 200, and 300 mg doses of disulfiram, respectively. The mean plasma concentrations of Me-DTC at steady-state were proportional to the disulfiram doses given, compared within groups at different doses, and between groups at equal and different optimal doses of the drug. The concentrations of Me-DTC were significantly increased, as compared above, whereas the blood concentrations of acetaldehyde were not significantly increased.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在10名酒精性肝病患者单次口服400mg双硫仑(安塔布司)后,比较了二乙基二硫代氨基甲酸甲酯(Me-DDC)及其单硫类似物(Me-DTC)的消除动力学。持续监测受试者红细胞醛脱氢酶(ALDH)活性直至完全失活。在12名健康志愿者中,给予递增剂量的双硫仑然后用乙醇激发,研究了血浆中Me-DTC的个体稳态浓度、血液乙醛浓度与产生双硫仑-酒精反应所需双硫仑剂量之间的关系。Me-DDC的平均血浆峰浓度出现在1.8小时,其血浆半衰期为6.3小时。Me-DTC的相应值分别为3.3小时和11.2小时。这表明Me-DTC是由Me-DDC氧化形成的。在红细胞ALDH活性迅速下降(少于5天)的酗酒者中,Me-DTC的平均血浆峰浓度为278nmol·l-1,而在失活时间延长(7-20天)的受试者中,峰浓度低于检测限。健康志愿者分为三组,每组四人,分别在100mg(双硫仑)、200mg(双硫仑)和300mg(双硫仑)剂量下出现临床上有效的双硫仑-酒精反应。在不同剂量组内以及在药物的相同和不同最佳剂量组之间比较时,稳态下Me-DTC的平均血浆浓度与给予的双硫仑剂量成比例。与上述情况相比,Me-DTC的浓度显著增加,而血液中乙醛的浓度没有显著增加。(摘要截短至250字)

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