Key result
Acute oral methionine load significantly reduced arterial distensibility and compliance and altered flow-dependent vasodilatation compared to placebo (P<0.05).
Why the study?
Does acute hyperhomocysteinemia induced by oral methionine reduce arterial distensibility and compliance in healthy young males?
RCT (n=12)
Double-blind
Cross-over
Does acute hyperhomocysteinemia induced by oral methionine reduce arterial distensibility and compliance in healthy young males?
Acute hyperhomocysteinemia impairs arterial elasticity and endothelial function, an effect that appears mediated by oxidative stress and is preventable with antioxidant vitamins.
Warrants caution with acute methionine loads or supplements; confirms hyperhomocysteinemia impairs arterial function in young adults.
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 (100 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-iso-prostaglandin F2alpha 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 F2alpha excretion. CONCLUSIONS: Hyperhomocysteinemia seems responsible for altered arterial wall elasticity and for endothelial dysfunction. A pivotal role can be attributed to oxidative stress.
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Arcaro et al. (2004) conducted an RCT in Healthy (n=12). Methionine vs. Placebo was evaluated on Distensibility and compliance of common femoral and brachial arteries. Acute oral methionine load significantly reduced arterial distensibility and compliance and altered flow-dependent vasodilatation compared to placebo (P<0.05).
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