Folic acid treatment reduces elevated plasma levels of asymmetric dimethylarginine in hyperhomocysteinaemic subjects

被引:69
作者
Holven, KB [1 ]
Haugstad, TS
Holm, T
Aukrust, P
Ose, L
Nenseter, MS
机构
[1] Univ Hosp, Rikshosp, Internal Med Res Inst, Oslo, Norway
[2] Univ Hosp, Rikshosp, Lipid Clin, Oslo, Norway
[3] Univ Hosp, Rikshosp, Dept Cardiol, Oslo, Norway
[4] Univ Hosp, Rikshosp, Dept Med, Sect Clin Immunol & Infect Dis, Oslo, Norway
[5] Univ Hosp, Rikshosp, MSD Cardiovasc Res Ctr, Oslo, Norway
关键词
homocysteine; folic acid; asymmetric dimethylarginine; nitric-oxide-derived endproducts;
D O I
10.1079/BJN2002779
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Asymmetric dimethylarginine (ADMA), an endogenous inhibitor of NO synthase, has been suggested to be a novel risk factor for endothelial dysfunction. It has previously been reported that hyperhomocysteinaemia may be associated with impaired endothelium-dependent vasodilation and reduced plasma level of NO-derived endproducts (NOx). In the present study, plasma levels of arginine and ADMA were measured in twenty-one healthy control subjects, and in twenty-one hyperhomocysteinaemic subjects before and after 6 weeks and 12 months of folic acid supplementation, and compared with previously measured plasma NOx values in the hyperhomocysteinaemic subjects. Compared with control subjects, hyperhomocysteinaemic subjects had higher plasma levels of arginine and ADMA. More importantly, folic acid therapy significantly reduced plasma levels of arginine and ADMA. Furthermore, plasma levels of arginine and ADMA were positively correlated with plasma homocysteine levels and negatively correlated with plasma folate, as well as negatively correlated with plasma NOx. Our results suggest that ADMA may be a mediator of the atherogenic effects of homocysteine.
引用
收藏
页码:359 / 363
页数:5
相关论文
共 29 条
[1]  
Bellamy MF, 1999, EUR J CLIN INVEST, V29, P659, DOI 10.1046/j.1365-2362.1999.00527.x
[2]   Hyperhomocysteinemia after an oral methionine load acutely impairs endothelial function in healthy adults [J].
Bellamy, MF ;
McDowell, IFW ;
Ramsey, MW ;
Brownlee, M ;
Bones, C ;
Newcombe, RG ;
Lewis, MJ .
CIRCULATION, 1998, 98 (18) :1848-1852
[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]   An endogenous inhibitor of nitric oxide synthase regulates endothelial adhesiveness for monocytes [J].
Böger, RH ;
Bode-Böger, SM ;
Tsao, PS ;
Lin, PS ;
Chan, JR ;
Cooke, JP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (07) :2287-2295
[5]  
Böger RH, 2001, CLIN SCI, V100, P161, DOI 10.1042/CS20000173
[6]   Plasma concentration of asymmetric dimethylarginine, an endogenous inhibitor of nitric oxide synthase, is elevated in monkeys with hyperhomocyst(e)inemia or hypercholesterolemia [J].
Böger, RH ;
Bode-Böger, SM ;
Sydow, K ;
Heistad, DD ;
Lentz, SR .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (06) :1557-1564
[7]   A QUANTITATIVE ASSESSMENT OF PLASMA HOMOCYSTEINE AS A RISK FACTOR FOR VASCULAR-DISEASE - PROBABLE BENEFITS OF INCREASING FOLIC-ACID INTAKES [J].
BOUSHEY, CJ ;
BERESFORD, SAA ;
OMENN, GS ;
MOTULSKY, AG .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (13) :1049-1057
[8]   FOLIC-ACID - AN INNOCUOUS MEANS TO REDUCE PLASMA HOMOCYSTEINE [J].
BRATTSTROM, LE ;
ISRAELSSON, B ;
JEPPSSON, JO ;
HULTBERG, BL .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1988, 48 (03) :215-221
[9]   Acute hyperhomocysteinaemia and endothelial dysfunction [J].
Chambers, JC ;
McGregor, A ;
Jean-Marie, J ;
Kooner, JS .
LANCET, 1998, 351 (9095) :36-37
[10]  
*DEP HLTH HUM SERV, 1993, REP EXP PAN DET EV T