Oral arginine reduces systemic blood pressure in type 2 diabetes: Its potential role in nitric oxide generation

被引:41
作者
Huynh, NT [1 ]
Tayek, JA [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Harbor Med Ctr, Dept Internal Med, Torrance, CA USA
关键词
blood pressure; nitric oxide; arginine;
D O I
10.1080/07315724.2002.10719245
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
Objectives: Arginine is converted in the endothelial cells to nitric oxide (NO) and citrulline. NO is a potent vasodilator in humans, but diabetics may have a reduced generation of NO which results in endothelial dysfunction. The aim of this study was to evaluate the effects of oral arginine on nitric oxide production, counter-regulatory hormones and blood pressure in mildly hypertensive type 2 diabetic patients. Methods: A prospective, crossover clinical trial was performed over a three-day stay in the General Clinical Research Center. Six patients with type 2 diabetes mellitus and mild hypertension consented and were given orally three grams of arginine per hour for 10 hours on either day 2 or day 3. On both days 2 and 3, blood pressure was monitored between 5 AM and 4 PM and mean pressure determined. Results: Oral arginine increased plasma citrulline from 31.3 +/- 6.0 to 41.5 +/- 6.0 mumol/L (mean +/- SEM; p < 0.05) which may reflect an increased conversion of arginine into NO and citrulline. Arginine reduced systolic BP from 135 +/- 7 to 123 +/- 8 mmHg; p < 0.05. Diastolic BP fell from 86.9 +/- 1.7 to 80.7 +/- 2.4 mmHg; p < 0.05). The reduction in BP was noted to occur two hours after starting oral arginine, and BP returned to normal within one hour of stopping the arginine. The oral arginine had no effect on C-peptide, insulin or other hormone concentrations. Conclusions: These data suggest that oral arginine may increase endothelial nitric oxide synthase (NOS) to increase vascular NO and temporally reduce blood pressure in mildly hypertensive type 2 diabetic patients.
引用
收藏
页码:422 / 427
页数:6
相关论文
共 26 条
[1]  
Arkhipova M M, 2000, Vestn Oftalmol, V116, P23
[2]   Haemodynamic effects of inhibition of nitric oxide synthase and of L-arginine at rest and during exercise [J].
Brett, SE ;
Cockcroft, JR ;
Mant, TGK ;
Ritter, JM ;
Chowienczyk, PJ .
JOURNAL OF HYPERTENSION, 1998, 16 (04) :429-435
[3]   Effects of low-dose and high-dose glucagon on glucose production and gluconeogenesis in humans [J].
Chhibber, VL ;
Soriano, C ;
Tayek, JA .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (01) :39-46
[4]   Oral L-arginine improves endothelium-dependent dilation in hypercholesterolemic young adults [J].
Clarkson, P ;
Adams, MR ;
Powe, AJ ;
Donald, AE ;
McCredie, R ;
Robinson, J ;
McCarthy, SN ;
Keech, A ;
Celermajer, DS ;
Deanfield, JE .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (08) :1989-1994
[5]  
Felaco M, 2001, ANN CLIN LAB SCI, V31, P179
[6]   Nitric oxide may be required to prevent hypertension at the onset of diabetes [J].
Fitzgerald, SM ;
Brands, MW .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 279 (04) :E762-E768
[7]   Hypertension in L-NAME-treated diabetic rats depends on an intact sympathetic nervous system [J].
Fitzgerald, SM ;
Brands, MW .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 282 (04) :R1070-R1076
[8]  
Giugliano D, 1997, CIRCULATION, V95, P1783
[9]   Tetrahydrobiopterin improves endothelium-dependent vasodilation by increasing nitric oxide activity in patients with Type II diabetes mellitus [J].
Heitzer, T ;
Krohn, K ;
Albers, S ;
Meinertz, T .
DIABETOLOGIA, 2000, 43 (11) :1435-1438
[10]  
Hink U, 2001, CIRC RES, V88, pE14