Johansson B, Angelo H R, Christensen J K, Møller I W, Rønsted P
Department of Clinical Chemistry, General Hospital, Malmö, Sweden.
Pharmacol Toxicol. 1991 Mar;68(3):166-70. doi: 10.1111/j.1600-0773.1991.tb01216.x.
The study was designed to elucidate the basic pharmacological and biochemical effects of the disulfiram dose (Antabus) provoking disulfiram-alcohol reaction (DAR) in 52 human volunteers after ethanol challenge. Disulfiram was given daily in increasing doses (1, 100, 200, and 300 mg) in successive 14 day periods, with ethanol challenge at the end of each period, until a DAR was achieved. Irrespective of dose (except the 1 mg dose), the DAR was always accompanied by almost complete inactivation (about 97%) of aldehyde dehydrogenase (ALDH) activity in erythrocytes, plasma concentrations of diethyldithiocarbamic acid methyl ester (Me-DDC) in the range of 8-472 nmol/l and accumulated plasma concentrations of acetaldehyde in the range of 7-197 mumol/l. In four of the volunteers, the cardiovascular effects of the DAR were recorded as a decrease in diastolic blood pressure (14-47 mmHg) and an increase in pulse rate (9-40 beats/min.), accompanied by a two- to fourfold increase in the plasma concentrations of adrenaline and noradrenaline. The enzyme kinetics of ALDH in erythrocytes were regularly analysed in eight volunteers during DSF intake. In addition to the expected decrease in oxidizing capacity, the Km values were also impaired, which suggests that the inhibitor is implicated in an active site directed reaction.
该研究旨在阐明双硫仑剂量(安塔布司)在52名人类志愿者乙醇激发后引发双硫仑-酒精反应(DAR)的基本药理和生化作用。双硫仑在连续14天的时间段内每日递增剂量(1、100、200和300毫克)给药,在每个时间段结束时进行乙醇激发,直至出现DAR。无论剂量如何(1毫克剂量除外),DAR总是伴随着红细胞中醛脱氢酶(ALDH)活性几乎完全失活(约97%)、血浆中二乙基二硫代氨基甲酸甲酯(Me-DDC)浓度在8-472纳摩尔/升范围内以及血浆中乙醛累积浓度在7-197微摩尔/升范围内。在4名志愿者中,记录到DAR的心血管效应为舒张压降低(14-47毫米汞柱)和脉搏率增加(9-40次/分钟),同时血浆中肾上腺素和去甲肾上腺素浓度增加两到四倍。在8名志愿者服用双硫仑期间定期分析红细胞中ALDH的酶动力学。除了预期的氧化能力降低外,米氏常数(Km值)也受到损害,这表明抑制剂参与了活性位点导向反应。