Age-associated impairment in vasorelaxation to fluid shear stress in the female vasculature is improved by TNF-α antagonism

被引:49
作者
Arenas, IA
Xu, Y
Davidge, ST
机构
[1] Univ Alberta, Perinatal Res Ctr, Dept Obstet & Gynecol, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Perinatal Res Ctr, Dept Physiol, Edmonton, AB T6G 2S2, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2006年 / 290卷 / 03期
关键词
tumor necrosis factor-alpha; estrogen deficiency; flow dilation; nitric oxide; endothelium;
D O I
10.1152/ajpheart.00990.2005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aging is associated with alterations in vascular homeostasis, including a reduction in flow-mediated vasodilation, which in women is related to the onset of menopause. We previously found that in female animals, aging is associated with an increase in TNF-alpha. Thus we investigated the role of in vivo TNF-alpha inhibition on vascular responses to shear stress in aging female rats. Mesenteric arteries (similar to 150 mu m) were isolated from young (3 mo) and ovariectomized Sprague-Dawley female rats approaching reproductive senescence (12 mo) treated with either placebo or a TNF-alpha inhibitor (etanercept; 0.3 mg/kg) and were mounted on a pressure myograph system. Vessels were equilibrated at an intraluminal pressure of 60 mmHg and then preconstricted with phenylephrine at similar to 70% of their initial diameter. Perfusate flow was increased in steps from 0 to 150 mu l/min. Compared with young vessels, aged vessels have a decrease in flow-mediated dilation [maximal dilation (means +/- SE): 52 +/- 4 vs. 24 +/- 15%; P < 0.05], which was improved by TNF-alpha inhibition. Moreover, in aged vessels maximal dilation to flow was achieved at higher levels of shear stress compared with young vessels. In all groups, flow-mediated dilation was abolished by either endothelial removal or nitric oxide synthase inhibition with N-G-nitro-L-arginine methyl ester. However, the modulation by N-G-nitro-L-arginine methyl ester was reduced in vessels from aged animals compared with young animals but was improved in the etanercept- treated aged animals. In vivo chronic TNF-alpha inhibition improves flow-mediated arterial dilation in resistance arteries of aged female animals.
引用
收藏
页码:H1259 / H1263
页数:5
相关论文
共 40 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]   Chronic tumor necrosis factor-α inhibition enhances NO modulation of vascular function in estrogen-deficient rats [J].
Arenas, IA ;
Armstrong, SJ ;
Xu, Y ;
Davidge, ST .
HYPERTENSION, 2005, 46 (01) :76-81
[3]   Effects of chronic PGHS-2 inhibition on PGHS-dependent vasoconstriction in the aged female rat [J].
Armstrong, SJ ;
Xu, Y ;
Davidge, ST .
CARDIOVASCULAR RESEARCH, 2004, 61 (02) :333-338
[4]   Estrogen replacement reduces PGHS-2-dependent vasoconstriction in the aged rat [J].
Armstrong, SJ ;
Zhang, YL ;
Stewart, KG ;
Davidge, ST .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (03) :H893-H898
[5]   Independent association between inflammatory markers (C-reactive protein, interleukin-6, and TNF-α) and essential hypertension [J].
Bautista, LE ;
Vera, LM ;
Arenas, IA ;
Gamarra, G .
JOURNAL OF HUMAN HYPERTENSION, 2005, 19 (02) :149-154
[6]  
BEVAN JA, 1988, BLOOD VESSELS, V25, P101
[7]  
BEVAN JA, 1990, BLOOD VESSELS, V27, P202
[8]   Tumour necrosis factor-α, inflammatory biomarkers, and atherogenesis [J].
Blake, GJ ;
Ridker, PM .
EUROPEAN HEART JOURNAL, 2002, 23 (05) :345-347
[9]   Flow-dependent regulation of endothelial nitric oxide synthase: role of protein kinases [J].
Boo, YC ;
Jo, H .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 285 (03) :C499-C508
[10]   Shear stress stimulates phosphorylation of endothelial nitric-oxide synthase at Ser1179 by Akt-independent mechanisms -: Role of protein kinase A [J].
Boo, YC ;
Sorescu, G ;
Boyd, N ;
Shiojima, L ;
Walsh, K ;
Du, J ;
Jo, HJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (05) :3388-3396