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DOI 10.1590/s0100-879x2004000900001

Медицинская библиотека · Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2004

Wine, alcohol and atherosclerosis: clinical evidences and mechanisms.

da Luz P L, Coimbra S R

СтатьяПоддержка исследования: вне правительства СШАОбзорПеревод пока не подготовлен

Аннотация

Atherosclerosis is a chronic inflammatory disease which may cause obstructions of the coronary, cerebral and peripheral arteries. It is typically multifactorial, most often dependent on risk factors such as hypercholesterolemia, diabetes, smoking, hypertension, sedentarism, and obesity. It is the single main cause of death in most developed countries due to myocardial infarction, angina, sudden death, and heart failure. Several epidemiological studies suggest that moderate alcohol intake, especially red wine, decrease cardiac mortality due to atherosclerosis. The alcohol effect is described by a J curve, suggesting that moderate drinkers may benefit while abstainers and heavy drinkers are at higher risk. Experimental studies indicate that most beneficial effects of drinking are attributable to flavonoids that are present in red wine, purple grape juice and several fruits and vegetables. The mechanisms include antiplatelet actions, increases in high-density lipoprotein, antioxidation, reduced endothelin-1 production, and increased endothelial nitric oxide synthase expression which causes augmented nitric oxide production by endothelial cells. These findings lead to the concept that moderate red wine drinking, in the absence of contraindications, may be beneficial to patients who are at risk of atherosclerotic cardiovascular events. Moreover, a diet based on fruits and vegetables containing flavonoids may be even more beneficial.

Для цитирования: da Luz P L, Coimbra S R. Wine, alcohol and atherosclerosis: clinical evidences and mechanisms.. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas. 2004. DOI: 10.1590/s0100-879x2004000900001.

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