Asymmetric dimethylarginine (ADMA) in vascular, renal and hepatic disease and the regulatory role of L-arginine on its metabolism

被引:68
作者
Wilcken, David E. L. [1 ]
Sim, Ah Slew
Wang, Jun
Wang, Xing Li
机构
[1] Univ New S Wales, Dept Cardiovasc Med, Sydney, NSW, Australia
[2] Prince Wales Hosp, Sydney, NSW, Australia
[3] Baylor Coll Med, Michael E DeBakey Dept Surg, Div Cardiothorac Surg, Houston, TX 77030 USA
关键词
asymmetric dimethylarginine; L-arginine; nitric oxide; vascular risk; renal function; hepatic function;
D O I
10.1016/j.ymgme.2007.04.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Asymmetric dimethylarginine (ADMA), an inhibitor of nitric oxide synthase (NOS), has been identified as a new and emerging contributor to, or marker for, cardiovascular risk. The ADMA-mediated regulation of nitric oxide (NO) production is determined by the quantitative bioavailability of intracellular and extracellular ADMA. Dimethylarginine dimethylaminohydrolase (DDAH), which is ubiquitously expressed in tissues, especially liver and kidney, converts the majority of the ADMA to citrulline. In this review, we discuss a new regulatory mechanism for the metabolism of ADMA in which L-arginine acts as a competitive inhibitor of DDAH activity. This novel regulatory pathway is consistent with ADMA contributing to cardiovascular risk when levels are increased but not when levels are within the normal range. The pathway then has a physiological role in the regulation of NO production by preventing overproduction of NO. The regulatory role Of L-arginine on ADMA may explain the unexpected outcomes in Some L-arginine supplementation studies. This paper also reviews associations between the metabolism of ADMA and insulin resistance, smoking and homocysteine which are all associated with an increased risk of vascular disease. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:309 / 317
页数:9
相关论文
共 81 条
[21]   Cardiovascular effects of systemic nitric oxide synthase inhibition with asymmetrical dimethylarginine in humans [J].
Kielstein, JT ;
Impraim, B ;
Simmel, S ;
Bode-Böger, SM ;
Tsikas, D ;
Frölich, JC ;
Hoeper, MM ;
Haller, H ;
Fliser, D .
CIRCULATION, 2004, 109 (02) :172-177
[22]  
Kielstein JT, 1999, J AM SOC NEPHROL, V10, P594
[23]  
Kielstein JT, 2002, J AM SOC NEPHROL, V13, P170, DOI 10.1681/ASN.V131170
[24]   Relationship of asymmetric dimethylarginine to dialysis treatment and atherosclerotic disease [J].
Kielstein, JT ;
Bode-Böger, SM ;
Frölich, JC ;
Haller, H ;
Böger, RH .
KIDNEY INTERNATIONAL, 2001, 59 :S9-S13
[25]   Severity of HCV-induced liver damage alters glucose homeostasis in noncirrhotic patients with chronic HCV infection [J].
Konrad, T ;
Zeuzem, S ;
Toffolo, G ;
Vicini, P ;
Teuber, G ;
Briem, D ;
Lormann, J ;
Lenz, T ;
Herrmann, G ;
Berger, A ;
Cobelli, C ;
Usadel, KH .
DIGESTION, 2000, 62 (01) :52-59
[26]   Weight loss reduces circulating asymmetrical dimethylarginine concentrations in morbidly obese women [J].
Krzyzanowska, K ;
Mittermayer, F ;
Kopp, HP ;
Wolzt, M ;
Schernthaner, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (12) :6277-6281
[27]   The synthesis and metabolism of asymmetric dimethylarginine (ADMA) [J].
Leiper, JM ;
Vallance, P .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 62 (Suppl 1) :33-38
[28]   Identification of two human dimethylarginine dimethylaminohydrolases with distinct tissue distributions and homology with microbial arginine deiminases [J].
Leiper, JM ;
Maria, JS ;
Chubb, A ;
MacAllister, RJ ;
Charles, IG ;
Whitley, GSJ ;
Vallance, P .
BIOCHEMICAL JOURNAL, 1999, 343 :209-214
[29]   Hyperhomocysteinemia, endothelial dysfunction, and cardiovascular risk: the potential role of ADMA [J].
Lentz, SR ;
Rodionov, RN ;
Dayal, S .
ATHEROSCLEROSIS SUPPLEMENTS, 2003, 4 (04) :61-65
[30]   Plasma concentrations of nitric oxide and asymmetric dimethylarginine in human alcoholic cirrhosis [J].
Lluch, P ;
Torondel, B ;
Medina, P ;
Segarra, G ;
del Olmo, JA ;
Serra, MA ;
Rodrigo, JM .
JOURNAL OF HEPATOLOGY, 2004, 41 (01) :55-59