Impaired NO-dependent vasodilation in patients with Type II (non-insulin-dependent) by acute administration diabetes mellitus is restored of folate

被引:105
作者
van Etten, RW
de Koning, EJP
Verhaar, MC
Gaillard, CAJM
Rabelink, TJ
机构
[1] Univ Utrecht, Ctr Med, Dept Vasc Med & Diabet, NL-3584 CX Utrecht, Netherlands
[2] Eemland Hosp, Dept Internal Med, Amersfoort, Netherlands
关键词
nitric oxide; plethysmography; vasomotion; Type II diabetes mellitus; folate;
D O I
10.1007/s00125-002-0862-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. Patients with diabetes are characterised by endothelial dysfunction and cardiovascular mortality. In particular endothelium-derived nitric oxide has emerged as a first line mechanism against atherosclerosis. Hyperglycaemia causes oxygen radical stress but has also been associated with endothelial nitric oxide synthase uncoupling, both lead to decreased nitric oxide-availability. We recently showed that folate reverses eNOS uncoupling in vitro. Therefore we hypothesise that folate improves endothelial function in Type II (non-insulin-dependent) diabetes mellitus in vivo. Methods. Using forearm plethysmography, we evaluated the effect of local, intra-arterial administration of 5-methyltetrahydrofolate (5-MTHF, the active form of folic acid, 1 mug/100 ml FAV/min) on forearm blood flow in 23 patients with Type II diabetes and 21 control subjects, matched for age, sex, blood pressure, body mass index, weight and smoking habits. Serotonin as a stimulator of nitric oxide-dependent vasodilation and sodium nitroprusside as a stimulator of endothelium-independent vasodilation were infused. Results. Serotonin-induced vasodilation was blunted (53+/-30 vs 102+/-66 M/C%, p<0.005) and nitroprusside-induced vasodilation was mildly reduced (275 146 vs 391 203 M/C%, p<0.05) in patients with Type II diabetes compared to control subjects. 5-MTHF improved nitric oxide-mediated vasodilation (from 53 30 to 88 59 M/C%, p<0.05) in patients with Type II diabetes mellitus. As expected, 5-MTHF had no effect on forearm blood flow in control subjects. Conclusion/interpretation. These data imply that folate can be used to improve nitric oxide status and to restore endothelial dysfunction in patients with Type 11 diabetes. Our results provide a strong rationale for the initiation of studies that investigate whether supplementation with folic acid prevents future cardiovascular events in this patient group.
引用
收藏
页码:1004 / 1010
页数:7
相关论文
共 48 条
[1]   Long-term follow-up of patients with mild coronary artery disease and endothelial dysfunction [J].
Al Suwaidi, J ;
Hamasaki, S ;
Higano, ST ;
Nishimura, RA ;
Holmes, DR ;
Lerman, A .
CIRCULATION, 2000, 101 (09) :948-954
[2]  
Bellamy MF, 1999, EUR J CLIN INVEST, V29, P659, DOI 10.1046/j.1365-2362.1999.00527.x
[3]   MEASURING FOREARM BLOOD-FLOW AND INTERPRETING THE RESPONSES TO DRUGS AND MEDIATORS [J].
BENJAMIN, N ;
CALVER, A ;
COLLIER, J ;
ROBINSON, B ;
VALLANCE, P ;
WEBB, D .
HYPERTENSION, 1995, 25 (05) :918-923
[4]  
Brattström L, 1998, BMJ-BRIT MED J, V316, P894, DOI 10.1136/bmj.316.7135.894
[5]   Dietary folate from vegetables and citrus fruit decreases plasma homocysteine concentrations in humans in a dietary controlled trial [J].
Brouwer, IA ;
van Dusseldorp, M ;
West, CE ;
Meyboom, S ;
Thomas, CMG ;
Duran, M ;
Hof, KHV ;
Eskes, TKAB ;
Hautvast, JGAJ ;
Steegers-Theunissen, RPM .
JOURNAL OF NUTRITION, 1999, 129 (06) :1135-1139
[6]   SEROTONIN-INDUCED VASODILATATION IN THE HUMAN FOREARM IS MEDIATED BY THE NITRIC OXIDE-PATHWAY - NO EVIDENCE FOR INVOLVEMENT OF THE 5-HT3-RECEPTOR [J].
BRUNING, TA ;
CHANG, PC ;
BLAUW, GJ ;
VERMEIJ, P ;
VANZWIETEN, PA .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1993, 22 (01) :44-51
[7]   ADVANCED GLYCOSYLATION PRODUCTS QUENCH NITRIC-OXIDE AND MEDIATE DEFECTIVE ENDOTHELIUM-DEPENDENT VASODILATATION IN EXPERIMENTAL DIABETES [J].
BUCALA, R ;
TRACEY, KJ ;
CERAMI, A .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (02) :432-438
[8]  
Ceriello A, 1999, DIABETES NUTR METAB, V12, P42
[9]   EFFECT OF N-G-MONOMETHYL-L-ARGININE ON KININ-INDUCED VASODILATION IN THE HUMAN FOREARM [J].
COCKCROFT, JR ;
CHOWIENCZYK, PJ ;
BRETT, SE ;
RITTER, JM .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1994, 38 (04) :307-310
[10]  
Cosentino F, 1997, CIRCULATION, V96, P25