Determination of arginine and asymmetric dimethylarginine (ADMAL) in human plasma by liquid chromatography/mass spectrometry with the isotope dilution technique

被引:58
作者
Martens-Lobenhoffer, J
Krug, O
Bode-Böger, SM
机构
[1] Otto Von Guericke Univ, Univ Hosp, Inst Clin Pharmacol, D-39120 Magdeburg, Germany
[2] Univ Magdeburg, Inst Chem, D-39106 Magdeburg, Germany
来源
JOURNAL OF MASS SPECTROMETRY | 2004年 / 39卷 / 11期
关键词
arginine dimethylarginine; liquid chromatography/mass spectrometry; stable isotope dilution; human plasma;
D O I
10.1002/jms.684
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Arginine (ARG) is a substrate for endogenous nitric oxide (NO) production whereas its metabolite, asymmetric dimethylarginine (ADMA), acts as an inhibitor. Sufficient NO production is essential for cardiovascular key functions, thus elevated concentration levels of ADMA are related to a range of cardiovascular diseases. Owing to the lack of reliable methods for the measurement of ARG and ADMA in human plasma, concentration values determined with these methods can differ considerably. We present here a simple and very robust liquid chromatographic/mass spectrometric method for the determination of ARG and ADMA utilizing isotope-labeled internal standards. Sample preparation requires only protein precipitation; the analytes were derivatized with o-phthalaldehyde-mercaptoethanoI and separated on a reversed-phase C-18 column with gradient elution. The analytes were detected with an electrospray ionization ion trap instrument working in the full-scan single mass spectrometry mode. Concentration values obtained with this method for healthy controls were ARG = 63.9 +/- 23.9 mum and ADMA = 0.355 +/- 0.066 mum, with a normal range for ADMA from 0.225 to 0.485 mum. The corresponding values for end-stage chronic renal failure patients are ARG = 48.1 +/- 18.5 mum, p < 0.01 and ADMA = 0.673 +/- 0.134 m, p < 0.001. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:1287 / 1294
页数:8
相关论文
共 22 条
[1]   Asymmetric dimethylarginine causes hypertension and cardiac dysfunction in humans and is actively metabolized by dimethylarginine dimethylaminohydrolase [J].
Achan, V ;
Broadhead, M ;
Malaki, M ;
Whitley, G ;
Leiper, J ;
MacAllister, R ;
Vallance, P .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (08) :1455-1459
[2]  
Anderstam B, 1997, J AM SOC NEPHROL, V8, P1437
[3]   Asymmetric dimethylarginine (ADMA):: A novel risk factor for endothelial dysfunction -: Its role in hypercholesterolemia [J].
Böger, RH ;
Bode-Böger, SM ;
Szuba, A ;
Tsao, PS ;
Chan, JR ;
Tangphao, O ;
Blaschke, TF ;
Cooke, JP .
CIRCULATION, 1998, 98 (18) :1842-1847
[4]   Determination of asymmetrical dimethylarginine by capillary electrophoresis-laser-induced fluorescence [J].
Caussé, E ;
Siri, N ;
Arnal, JF ;
Bayle, C ;
Malatray, P ;
Valdiguié, P ;
Salvayre, R ;
Couderc, F .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2000, 741 (01) :77-83
[5]   Determination of N-G,N-G-dimethylarginine in human plasma by high-performance liquid chromatography [J].
Chen, BM ;
Xia, LW ;
Zhao, RQ .
JOURNAL OF CHROMATOGRAPHY B, 1997, 692 (02) :467-471
[6]   Does ADMA cause endothelial dysfunction? [J].
Cooke, JP .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (09) :2032-2037
[7]   Serum concentrations of asymmetric (ADMA) and symmetric (SDMA) dimethylarginine in patients with chronic kidney diseases [J].
Fleck, C ;
Schweitzer, F ;
Karge, E ;
Busch, M ;
Stein, G .
CLINICA CHIMICA ACTA, 2003, 336 (1-2) :1-12
[8]  
Kielstein JT, 1999, J AM SOC NEPHROL, V10, P594
[9]   Simultaneous detection of arginine, asymmetric dimethylarginine, symmetric dimethylarginine and citrulline in human plasma and urine applying liquid chromatography-mass spectrometry with very straightforward sample preparation [J].
Martens-Lobenhoffer, J ;
Bode-Böger, SM .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 798 (02) :231-239
[10]   High-performance liquid chromatographic determination of nitric oxide synthase-related arginine derivatives in vitro and in vivo [J].
Meyer, J ;
Richter, N ;
Hecker, M .
ANALYTICAL BIOCHEMISTRY, 1997, 247 (01) :11-16