Acute hyperhomocysteinemia induces a reduction in arterial distensibility and compliance

被引:28
作者
Arcaro, G
Fava, C
Dagradi, R
Faccini, G
Gaino, S
Degan, M
Lechi, C
Lechi, A
Minuz, P
机构
[1] Univ Verona, Dept Med, I-37100 Verona, Italy
[2] Univ Verona, Dept Surg Sci, I-37100 Verona, Italy
[3] Univ Verona, Dept Morphol Sci, I-37100 Verona, Italy
关键词
arterial compliance; arterial distensibility; arterial elasticity; endothelium; homocysteine; hypertension; isoprostanes;
D O I
10.1097/00004872-200404000-00021
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objective The aim of the study was to evaluate the effects of acute hyperhomocysteinemia on distensibility and compliance of large peripheral arteries. Isoprostanes generation and antioxidant vitamins were used to assess the role of oxidative stress. Design A cross-over, double-blind study on distensibility (DC: distensibility coefficient) and compliance (CC: cross-sectional compliance) of common femoral and brachial arteries was performed in 12 healthy young male volunteers by means of a wall track system before and 4 h after a single oral methionine (1100 mg/kg) or placebo administration. The effects of methionine load were investigated also after oral administration of vitamin C (1g/day) and vitamin E (800 mg/day) for 8 consecutive days. Results Oral methionine induced a significant increase in plasmatic levels of homocysteine. Distensibility and compliance of brachial and femoral arteries were significantly reduced after methionine load in comparison to placebo. This acute impairment of arterial wall mechanical properties was associated to endothelial dysfunction, since altered flow-dependent vasodilatation (P < 0.05 versus placebo) was observed in the same arterial districts. A significant increase in urinary 8-isoprostaglandin F(2)alpha was observed after methionine. Pretreatment with vitamins C and E prevented the effects of methionine on femoral and brachial arteries as well as on urinary 8-iso-prostaglandin F(2)alpha excretion. Conclusions Hyperhomocysteinemia seems responsible for altered arterial wall elasticity and for endothelial dysfunction. A pivotal role can be attributed to oxidative stress. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:775 / 781
页数:7
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