Oxidative-stress-mediated arterial dysfunction in patients with peripheral arterial disease

被引:95
|
作者
Loffredo, L.
Marcoccia, A.
Pignatelli, P.
Andreozzi, P.
Borgia, M. C.
Cangemi, R.
Chiarotti, F.
Violi, Francesco
机构
[1] Univ Roma La Sapienza, Dept Expt Med & Pathol, Div Clin Med 4, I-00161 Rome, Italy
[2] Ist Super Sanita, Dept Cell Biol & Neurosci, I-00161 Rome, Italy
关键词
peripheral vascular disease; flow-mediated dilation; nitric oxide; oxidative stress; propionylcarnitine;
D O I
10.1093/eurheartj/ehl533
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims To investigate the existence of a relationship among flow-mediated dilation (FMD), nitric oxide (NO), and oxidative stress in patients with peripheral arterial disease (PAD), and to assess if the administration of an antioxidant was able to improve arterial dilatation. Methods and results We performed a cross-sectional study comparing FMD, 8-Hydroxy-2-deoxy-2-deoxyguanosine (8-CHdG), a marker of oxidative stress, and nitrite/nitrate (NOx) serum levels in a population of 25 PAD patients and 40 controls. In the second part of the study, 21 PAD patients were randomly allocated to a treatment sequence of 7 days of i.v. infusion of placebo or 6 g/day propionyl-L-carnitine (PLC) in a cross-over design. Compared with controls, patients with PAD had enhanced 8-OHdG serum levels (2.4 +/- 1.2 vs. 4.24 +/- 3.11 ng/mL; P < 0.001), reduced NOx (17.02 +/- 6.11 vs. 11.28 +/- 6.02 mu M; P < 0.001), and towered FMD (10.34 +/- 2.14 vs. 6.69 +/- 2.95; P < 0.001). PLC infusion was associated with an increase of FMD [from 6.6 +/- 0.6 to 11.1 +/- 1.2% (mean +/- SE), P = 0.004] and NOx (from 14.5 +/- 1.4 to 17.1 +/- 1.2 mu M; + 18%, P = 0.012) and a decrease of 8-CHdG (from 3.62 +/- 0.37 to 2.64 +/- 0.32 ng/mL; -27%, P < 0.001). No changes were observed after placebo treatment. Conclusion This study shows that in PAD patients, oxidative stress is implicated in determining reduced FMD.
引用
收藏
页码:608 / 612
页数:5
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