Mårdh G, Sjöquist B, Anggård E
J Neurochem. 1983 Jul;41(1):246-50. doi: 10.1111/j.1471-4159.1983.tb11835.x.
D,L(+/-)-4-Hydroxy-3-methoxyphenylglycol (HMPG) labelled with three deuterium atoms was used to study turnover of plasma free HMPG following an intravenous injection. Ten healthy men were given a pulse dose of either 4.3 mumol or 2.2 mumol of labelled HMPG ([2H3]HMPG piperazine salt). Plasma and urine levels of both endogenous and labelled HMPG were subsequently followed by gas chromatography-mass spectrometry with selected ion detection. Kinetic calculations based upon a single-compartment model were consistent with a monoexponential elimination of plasma free HMPG. The half-life of HMPG was 0.46 and 0.78 h (mean values in the two dose groups). The HMPG production rate was 2.01 and 2.35 mumol/hour, and the urinary excretion rate of HMPG (free and conjugated) was 0.48 and 0.47 mumol/h. The endogenous plasma level of free HMPG was 25 and 33 nmol/L. The results show that HMPG turns over rapidly and that HMPG is further metabolized extensively. About one-fourth of the HMPG produced is excreted in urine as free and conjugated HMPG.
用标记有三个氘原子的D,L(±)-4-羟基-3-甲氧基苯乙二醇(HMPG)研究静脉注射后血浆游离HMPG的周转率。给10名健康男性静脉注射4.3μmol或2.2μmol标记的HMPG([2H3]HMPG哌嗪盐)脉冲剂量。随后用选择离子检测的气相色谱-质谱法跟踪内源性和标记的HMPG的血浆和尿液水平。基于单室模型的动力学计算与血浆游离HMPG的单指数消除一致。HMPG的半衰期为0.46和0.78小时(两个剂量组的平均值)。HMPG的生成率为2.01和2.35μmol/小时,HMPG(游离和结合型)的尿排泄率为0.48和0.47μmol/小时。游离HMPG的内源性血浆水平为25和33nmol/L。结果表明,HMPG周转迅速,并且HMPG进一步被广泛代谢。所产生的HMPG约四分之一以游离和结合型HMPG的形式经尿液排泄。