Morris M E, Levy G
J Toxicol Clin Toxicol. 1983 Apr;20(2):107-14. doi: 10.3109/15563658308990056.
The purpose of this investigation was to determine the suitability of orally administered magnesium sulfate as a source of inorganic sulfate for counteracting the systemic depletion of sulfate caused by large doses of acetaminophen and certain other drugs that are metabolized to sulfate conjugates. Oral administration of 13.9 g magnesium sulfate U.S.P., in 4 equal hourly increments, to seven healthy men resulted in the urinary excretion (corrected for baseline excretion rate) of an amount of inorganic sulfate equivalent to 30.2 +/- 17.2 percent (mean +/- SD) of the dose during the first 24 hours. Excretion during the subsequent 48 hours was negligible. Six of the subjects experienced loose stools or diarrhea. Compared to sodium sulfate, magnesium sulfate appears to be absorbed less completely and more erratically, and to produce more adverse effects.
本研究的目的是确定口服硫酸镁作为无机硫酸盐来源,用于抵消大剂量对乙酰氨基酚及其他某些代谢为硫酸酯结合物的药物所导致的全身硫酸盐消耗的适用性。给7名健康男性每小时等量口服13.9 g美国药典级硫酸镁,分4次服用,结果在前24小时内,无机硫酸盐的尿排泄量(校正基线排泄率后)相当于给药量的30.2±17.2%(平均值±标准差)。随后48小时的排泄量可忽略不计。6名受试者出现了大便溏稀或腹泻。与硫酸钠相比,硫酸镁的吸收似乎更不完全且更不稳定,并且会产生更多不良反应。