Allopurinol and Nitric Oxide Activity in the Cerebral Circulation of Those With Diabetes

被引:25
作者
Dawson, Jesse [1 ]
Quinn, Terry [1 ]
Harrow, Craig [1 ]
Lees, Kennedy R. [1 ]
Weir, Christopher J. [3 ]
Cleland, Stephen J. [2 ]
Walters, Matthew R. [1 ]
机构
[1] Univ Glasgow, Western Infirm, Div Cardiovasc & Med Sci, Acute Stroke Unit, Glasgow G11 6NT, Lanark, Scotland
[2] Stobhill Hosp, Glasgow, Lanark, Scotland
[3] Univ Glasgow, Robertson Ctr Biostat, Glasgow G11 6NT, Lanark, Scotland
关键词
SYNTHASE INHIBITION; URIC-ACID;
D O I
10.2337/dc08-1179
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE - Type 2 diabetes increases risk of stroke, perhaps because of impaired cerebrovascular basal nitric oxide (NO) activity. We investigated whether this activity is improved by a 2-week course of the xanthine oxidase inhibitor allopurinol. RESEARCH DESIGN AND METHODS - We performed a randomized, double-blind, placebo-controlled crossover study. We measured the response to infusion of NG-monomethyl-L-arginine (L-NMMA) in males with type 2 diabetes before and after allopurinol or placebo. The primary end point was the change in internal carotid artery How following L-NMMA infusion, expressed as the area under the flow-per-time curve. RESULTS - We enrolled 14 participants. Allopurinol improved responses to L-NMMA when compared With responses associated With placebo (P = 0.032; median reduction in internal carotid artery How following L-NMMA of 3,144 ml [95% CI 375-7,143]). CONCLUSIONS - Xanthine oxidase inhibition With allopurinol appears to improve cerebral NO bioavailability, as evidenced by a greater response to infusion of L-NMMA.
引用
收藏
页码:135 / 137
页数:3
相关论文
共 11 条
[1]
Investigation into the sources of superoxide in human blood vessels - Angiotensin II increases superoxide production in human internal mammary arteries [J].
Berry, C ;
Hamilton, CA ;
Brosnan, J ;
Magill, FG ;
Berg, GA ;
McMurray, JJV ;
Dominiczak, AF .
CIRCULATION, 2000, 101 (18) :2206-2212
[2]
Allopurinol normalizes endothelial dysfunction in type 2 diabetics with mild hypertension [J].
Butler, R ;
Morris, AD ;
Belch, JJF ;
Hill, A ;
Struthers, AD .
HYPERTENSION, 2000, 35 (03) :746-751
[3]
Dawson J, 2007, CURR MED CHEM, V14, P1879
[4]
Uric acid and xanthine oxidase: future therapeutic targets in the prevention of cardiovascular disease? [J].
Dawson, Jesse ;
Walters, Matthew .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 62 (06) :633-644
[5]
Lipid-independent effects of statins on endothelial function and bioavailability of nitric oxide in hypercholesterolemic patients [J].
John, S ;
Schneider, MP ;
Delles, C ;
Jacobi, J ;
Schmieder, RE .
AMERICAN HEART JOURNAL, 2005, 149 (03) :473.e1-473.e10
[6]
DIABETES AND CARDIOVASCULAR-DISEASE - FRAMINGHAM-STUDY [J].
KANNEL, WB ;
MCGEE, DL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1979, 241 (19) :2035-2038
[7]
Association between diabetes and stroke subtype on survival and functional outcome 3 months after stroke - Data from the European BIOMED stroke project [J].
Megherbi, SE ;
Milan, C ;
Minier, D ;
Couvreur, G ;
Osseby, GV ;
Tilling, K ;
Di Carlo, A ;
Inzitari, D ;
Wolfe, CDA ;
Moreau, T ;
Giroud, M .
STROKE, 2003, 34 (03) :688-694
[8]
Blunted response to systemic nitric oxide synthase inhibition in the cerebral circulation of patients with Type 2 diabetes [J].
Nazir, FS ;
Alem, M ;
Small, M ;
Connell, JMC ;
Lees, KR ;
Walters, MR ;
Cleland, SJ .
DIABETIC MEDICINE, 2006, 23 (04) :398-402
[9]
Improvement in endothelial function by angiotensin-converting enzyme inhibition in non-insulin-dependent diabetes mellitus [J].
O'Driscoll, G ;
Green, D ;
Maiorana, A ;
Stanton, K ;
Colreavy, F ;
Taylor, R .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 33 (06) :1506-1511
[10]
Nitric oxide synthase inhibition in humans reduces cerebral blood flow but not the hyperemic response to hypercapnia [J].
White, RP ;
Deane, C ;
Vallance, P ;
Markus, HS .
STROKE, 1998, 29 (02) :467-472