Yao J K, Zhu P, Wilds D J, van Kammen D P
VA Pittsburgh Healthcare System, Western Psychiatric Institute and Clinic, PA, USA.
J Neural Transm (Vienna). 1997;104(8-9):967-75. doi: 10.1007/BF01285564.
Urinary 3-methoxy-4-hydroxyphenylglycol (MHPG) level may provide us with a biochemical index for central noradrenergic activity. Previous methods for assaying MHPG in urine often lacked specificity, sensitivity, cost-effectiveness or convenience. We now describe a simplified routine assay for urinary MHPG by high-pressure liquid chromatography using electrochemical detection. For convenience and cost-effectiveness within a typical batch assay of total MHPG, 0.5 mL of urine sample, 50 microL of glusulase and 4 micrograms iso-vanillyl alcohol (internal standard) were used to hydrolyze conjugated MHPG at 37 degrees C overnight. Alternatively, for a same-day operation, it is efficient to hydrolyze the sample at 50 degrees C for 3 hours. Each sample was separated isocratically on a reversed-phase column (Ultracarb 5 ODS) at 25 degrees C with the flow rate at 1 mL/min. Intra- and inter-assay coefficients of variation were found to be 4.0% (n = 10) and 5.0% (n = 27), respectively, for MHPG at a mean concentration of 1.9 mg/L. Sulfatase or glucuronidase can be substituted for glusulase to obtain either sulfate- or glucuronide-conjugated MHPG. This procedure requires smaller sample amounts and less preparation time without compromising sensitivity and reproducibility.
尿中3-甲氧基-4-羟基苯乙二醇(MHPG)水平可为我们提供中枢去甲肾上腺素能活性的生化指标。以往测定尿中MHPG的方法往往缺乏特异性、敏感性、成本效益或便利性。我们现在描述一种使用电化学检测的高压液相色谱法简化的尿中MHPG常规检测方法。为了在典型的总MHPG批量检测中方便且具有成本效益,使用0.5 mL尿样、50 μL葡萄糖苷酶和4微克异香草醇(内标)在37℃下过夜水解结合型MHPG。或者,对于当日操作,在50℃下将样品水解3小时效率更高。每个样品在25℃下于反相柱(Ultracarb 5 ODS)上进行等度分离,流速为1 mL/分钟。对于平均浓度为1.9 mg/L的MHPG,批内和批间变异系数分别为4.0%(n = 10)和5.0%(n = 27)。硫酸酯酶或葡萄糖醛酸酶可替代葡萄糖苷酶以获得硫酸酯或葡萄糖醛酸结合型MHPG。该方法所需样品量较小,制备时间较短,且不影响灵敏度和重现性。