The Glu298Asp polymorphism of the NOS 3 gene as a determinant of the baseline production of nitric oxide

被引:222
作者
Veldman, BA
Spiering, W
Doevendans, PA
Vervoort, G
Kroon, AA
de Leeuw, PW
Smits, P
机构
[1] Univ Nijmegen, Med Ctr, Dept Pharmacol Toxicol 233, NL-6500 HB Nijmegen, Netherlands
[2] Univ Nijmegen, Med Ctr, Dept Internal Med, NL-6500 HB Nijmegen, Netherlands
[3] Univ Nijmegen, Med Ctr, Dept Nephrol, NL-6500 HB Nijmegen, Netherlands
[4] Univ Hosp Maastricht, Cardiovasc Res Inst, Dept Internal Med, Maastricht, Netherlands
[5] Univ Hosp Maastricht, Cardiovasc Res Inst, Dept Cardiol, Maastricht, Netherlands
关键词
genetics; plethysmography; endothelium-dependent vasodilation; ecNOS; norepinephrine; nitric oxide;
D O I
10.1097/00004872-200210000-00022
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Rationale The endothelial nitric oxide synthase Glu298Asp polymorphism has been suggested to play a role in the development of hypertension, atherosclerosis and coronary artery disease. Objective To investigate functional differences between the various genotypes with respect to basal nitric oxide (NO) production, we estimated the response to endothelial NO synthase (ecNOS) inhibition by infusion of increasing doses of N-G-monomethyl-L-arginine (L-NMMA) into the brachial artery during venous occlusion plethysmography. Methods In 41 healthy subjects forearm blood flow responses to intra-arterial infusion of increasing doses of L-NMMA (0.05, 0.1 and 0.2 mg/min per dl) and norepinephrine (110, 20 and 40 ng/min per dl) were measured. The genotype of the ecNOS Glu298Asp polymorphism was assessed. Results Nineteen subjects had the Glu/Glu genotype, 19 subjects had the Glu/Asp genotype and three subjects had the Asp/Asp genotype. Groups were comparable concerning demographic, hemodynamic and possible confounding factors. Subjects with the Asp allele showed a reduced response to infusion Of L-NMMA as compared to subjects with the Glu/Glu genotype (ANOVA, P = 0.01). There was no significant difference in the response to infusion of the NO-independent vasoconstrictor, norepinephrine, between both groups. Conclusions The ecNOS Glu298Asp polymorphism is associated with reduced basal NO production and might therefore have functional implications in the development of atherosclerosis or hypertension. J Hypertens 20:2023-2027 (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:2023 / 2027
页数:5
相关论文
共 23 条
[1]   CHRONIC INHIBITION OF NITRIC-OXIDE PRODUCTION ACCELERATES NEOINTIMA FORMATION AND IMPAIRS ENDOTHELIAL FUNCTION IN HYPERCHOLESTEROLEMIC RABBITS [J].
CAYATTE, AJ ;
PALACINO, JJ ;
HORTEN, K ;
COHEN, RA .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (05) :753-759
[2]   A multilocus genotyping assay for candidate markers of cardiovascular disease risk [J].
Cheng, S ;
Grow, MA ;
Pallaud, C ;
Klitz, W ;
Erlich, HA ;
Visvikis, S ;
Chen, JJ ;
Pullinger, CR ;
Malloy, MJ ;
Siest, G ;
Kane, JP .
GENOME RESEARCH, 1999, 9 (10) :936-949
[3]  
DEMACKER PNM, 1980, CLIN CHEM, V26, P1775
[4]  
FISKERSTRAND T, 1993, CLIN CHEM, V39, P263
[5]   NITRIC OXIDE-GENERATING VASODILATORS AND 8-BROMO-CYCLIC GUANOSINE-MONOPHOSPHATE INHIBIT MITOGENESIS AND PROLIFERATION OF CULTURED RAT VASCULAR SMOOTH-MUSCLE CELLS [J].
GARG, UC ;
HASSID, A .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (05) :1774-1777
[6]   A common variant of the endothelial nitric oxide synthase (Glu298→Asp) is a major risk factor for coronary artery disease in the UK [J].
Hingorani, AD ;
Liang, CF ;
Fatibene, J ;
Lyon, A ;
Monteith, S ;
Parsons, A ;
Haydock, S ;
Hopper, RV ;
Stephens, NG ;
O'Shaughnessy, KM ;
Brown, MJ .
CIRCULATION, 1999, 100 (14) :1515-1520
[7]   INHIBITION OF LOW-DENSITY-LIPOPROTEIN OXIDATION BY NITRIC-OXIDE - POTENTIAL ROLE IN ATHEROGENESIS [J].
HOGG, N ;
KALYANARAMAN, B ;
JOSEPH, J ;
STRUCK, A ;
PARTHASARATHY, S .
FEBS LETTERS, 1993, 334 (02) :170-174
[8]   Lack of evidence for association between the endothelial nitric oxide synthase gene and hypertension [J].
Kato, N ;
Sugiyama, T ;
Morita, H ;
Nabika, T ;
Kurihara, H ;
Yamori, Y ;
Yazaki, Y .
HYPERTENSION, 1999, 33 (04) :933-936
[9]   NITRIC-OXIDE - AN ENDOGENOUS MODULATOR OF LEUKOCYTE ADHESION [J].
KUBES, P ;
SUZUKI, M ;
GRANGER, DN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :4651-4655
[10]   Nitric oxide synthase gene polymorphisms, blood pressure and aortic stiffness in normotensive and hypertensive subjects [J].
Lacolley, P ;
Gautier, S ;
Poirier, O ;
Pannier, B ;
Cambien, F ;
Benetos, A .
JOURNAL OF HYPERTENSION, 1998, 16 (01) :31-35