Endothelial nitric oxide synthase polymorphisms and hypertension

被引:73
作者
Hingorani, AD [1 ]
机构
[1] UCL, BHF Labs, Ctr Clin Pharmacol, London WC1E 6JF, England
关键词
D O I
10.1007/s11906-003-0006-0
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The human endothelial nitric oxide synthase (eNOS) gene is highly polymorphic. Evidence for the involvement of eNOS single nucleotide polymorphisms in the development of essential hypertension is limited, though the eNOS Glu298Asp polymorphism appears to influence the blood pressure response to exercise. This variant also influences endothelial function, with its effects becoming manifest during the adaptive vascular changes in pregnancy. Carriers of eNOS Asp298 may be at risk of developing pre-eclampsia. Molecular studies have indicated that intact eNOS Asp298 has equivalent enzymatic activity to eNOS Glu298, but undergoes selective proteolysis in native cells and tissues such that the steady state level of active eNOS may be reduced in carriers of this allele. Carriers of eNOS Asp298, particularly if exposed to adverse environmental influences on endothelial function, may be at increased risk of developing atherosclerosis and cerebrovascular disease.
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页码:19 / 25
页数:7
相关论文
共 69 条
[1]   Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene region [J].
Arngrimsson, R ;
Hayward, C ;
Nadaud, S ;
Baldursdottir, A ;
Walker, JJ ;
Liston, WA ;
Bjarnadottir, RI ;
Brock, DJH ;
Geirsson, RT ;
Connor, JM ;
Soubrier, F .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) :354-362
[2]   THE EFFECT OF NITRIC OXIDE-DONATING VASODILATORS ON MONOCYTE CHEMOTAXIS AND INTRACELLULAR CGMP CONCENTRATIONS IN-VITRO [J].
BATH, PMW .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 45 (01) :53-58
[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]   LACK OF EVIDENCE FOR LINKAGE OF THE ENDOTHELIAL-CELL NITRIC-OXIDE SYNTHASE GENE TO ESSENTIAL-HYPERTENSION [J].
BONNARDEAUX, A ;
NADAUD, S ;
CHARRU, A ;
JEUNEMAITRE, X ;
CORVOL, P ;
SOUBRIER, F .
CIRCULATION, 1995, 91 (01) :96-102
[5]  
CALVER A, 1992, J HYPERTENS, V10, P1025
[6]   FOREARM BLOOD-FLOW RESPONSES TO A NITRIC-OXIDE SYNTHASE INHIBITOR IN PATIENTS WITH TREATED ESSENTIAL-HYPERTENSION [J].
CALVER, A ;
COLLIER, J ;
VALLANCE, P .
CARDIOVASCULAR RESEARCH, 1994, 28 (11) :1720-1725
[7]   Selective defect in nitric oxide synthesis may explain the impaired endothelium-dependent vasodilation in patients with essential hypertension [J].
Cardillo, C ;
Kilcoyne, CM ;
Quyyumi, AA ;
Cannon, RO ;
Panza, JA .
CIRCULATION, 1998, 97 (09) :851-856
[8]   Combined effects of endothelial nitric oxide synthase gene polymorphism (G894T) and insulin resistance status on blood pressure and familial risk of hypertension in young adults: The Bogalusa Heart Study [J].
Chen, W ;
Srinivasan, SR ;
Elkasabany, A ;
Ellsworth, DL ;
Boerwinkle, E ;
Berenson, GS .
AMERICAN JOURNAL OF HYPERTENSION, 2001, 14 (10) :1046-1052
[9]   DIFFERENTIAL INHIBITION BY N(G)-MONOMETHYL-L-ARGININE OF VASODILATOR EFFECTS OF ACETYLCHOLINE AND METHACHOLINE IN HUMAN FOREARM VASCULATURE [J].
CHOWIENCZYK, PJ ;
COCKCROFT, JR ;
RITTER, JM .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (02) :736-738
[10]   PRESERVED ENDOTHELIUM-DEPENDENT VASODILATATION IN PATIENTS WITH ESSENTIAL-HYPERTENSION [J].
COCKCROFT, JR ;
CHOWIENCZYK, PJ ;
BENJAMIN, N ;
RITTER, JM .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (15) :1036-1040