Effect of L-arginine supplementation on NO production in man

被引:22
作者
Bode-Böger, SM [1 ]
机构
[1] Univ Hosp Otto von Guericke Univ, Inst Clin Pharmacol, D-39120 Magdeburg, Germany
关键词
oral L-arginine; L-arginine paradox; asymmetric dimethylarginine (ADMA);
D O I
10.1007/s00228-005-0004-z
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
L-arginine is the substrate for the enzyme nitric oxide synthase (NOS), which is responsible for the production of nitric oxide (NO), an endogenous messenger molecule involved in many of the processes associated with the development of atherosclerosis. Acute and chronic administration of L-arginine has been shown to improve endothelial function in animal models of hypercholesterolemia and atherosclerosis. Therefore, numerous studies have been conducted to elucidate whether dietary L-arginine supplementation can augment NO production in humans and thereby improve vascular health. In this review, the results of studies of intravenous and oral L-arginine supplementation with a wide spectrum of doses, study duration, and surrogate parameters of endothelial function are summarized. The pharmacokinetics of L-arginine have been investigated; side effects are rare and mostly mild and dose-dependent. Several possible mechanisms of action of L-arginine are discussed. An evaluation of L-arginine as a therapeutic agent from the point of view of a clinical pharmacologist is given.
引用
收藏
页码:91 / 99
页数:9
相关论文
共 76 条
[1]   No effect of an L-arginine-enriched medical food (HeartBars) on endothelial function and platelet aggregation in subjects with hypercholesterolemia [J].
Abdelhamed, AI ;
Reis, SE ;
Sane, DC ;
Brosnihan, KB ;
Preli, RB ;
Herrington, DM .
AMERICAN HEART JOURNAL, 2003, 145 (03) :E15
[2]   Cigarette smoking is associated with increased human monocyte adhesion to endothelial cells: Reversibility with oral L-arginine but not vitamin C [J].
Adams, MR ;
Jessup, W ;
Celermajer, DS .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 29 (03) :491-497
[3]   Oral L-arginine improves endothelium-dependent dilatation and reduces monocyte adhesion to endothelial cells in young men with coronary artery disease [J].
Adams, MR ;
McCredie, R ;
Jessup, W ;
Robinson, J ;
Sullivan, D ;
Celermajer, DS .
ATHEROSCLEROSIS, 1997, 129 (02) :261-269
[4]   ORAL L-ARGININE INHIBITS PLATELET-AGGREGATION BUT DOES NOT ENHANCE ENDOTHELIUM-DEPENDENT DILATION IN HEALTHY-YOUNG MEN [J].
ADAMS, MR ;
FORSYTH, CJ ;
JESSUP, W ;
ROBINSON, J ;
CELERMAJER, DS .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1995, 26 (04) :1054-1061
[5]   Oral L-arginine in patients with coronary artery disease on medical management [J].
Blum, A ;
Hathaway, L ;
Mincemoyer, R ;
Schenke, WH ;
Kirby, M ;
Csako, G ;
Waclawiw, MA ;
Panza, JA ;
Cannon, RO .
CIRCULATION, 2000, 101 (18) :2160-2164
[6]   Effects of oral L-arginine on endothelium-dependent vasodilation and markers of inflammation in healthy postmenopausal women [J].
Blum, A ;
Hathaway, L ;
Mincemoyer, R ;
Schenke, WH ;
Kirby, M ;
Csako, G ;
Waclawiw, MA ;
Panza, JA ;
Cannon, RO .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 35 (02) :271-276
[7]   Endocrine and lipid effects of oral L-arginine treatment in healthy postmenopausal women [J].
Blum, A ;
Cannon, RO ;
Costello, R ;
Schenke, WH ;
Csako, G .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 2000, 135 (03) :231-237
[8]  
Bode-Böger SM, 1999, J INVEST MED, V47, P43
[9]   Oral L-arginine improves endothelial function in healthy individuals older than 70 years [J].
Bode-Böger, SM ;
Muke, J ;
Surdacki, A ;
Brabant, G ;
Böger, RH ;
Frölich, JC .
VASCULAR MEDICINE, 2003, 8 (02) :77-81
[10]   L-arginine-induced vasodilation in healthy humans:: Pharmacokinetic-pharmacodynamic relationship [J].
Bode-Böger, SM ;
Böger, RH ;
Galland, A ;
Tsikas, D ;
Frölich, JC .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 46 (05) :489-497