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Atherosclerosis ; 212(1): 93-9, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20553794

ABSTRACT

AIM: The cholesterol-lowering properties of oats, largely ascribed to its contents of soluble fibers, beta-glucans, are well established, whereas effects on atherogenesis are less well elucidated. Oats also contains components with reported antioxidant and anti-inflammatory effects that may affect atherogenesis. In this work we examined effects of oat bran on plasma cholesterol, markers of inflammation, eNOS expression and development of atherosclerosis in LDL-receptor-deficient (LDLr(-/-)) mice. METHODS AND RESULTS: Female LDLr(-/-) mice were fed Western diet+/-oat bran. Two concentrations of oat bran (40 and 27%) were compared regarding effects on plasma lipids. There was a dose-dependent reduction of plasma cholesterol by 42 and 20% with 40 and 27% oat bran, respectively. Both concentrations also lowered plasma triglycerides (by 45 and 33%) and relative levels of plasma LDL+VLDL. The reduction of plasma lipids was accompanied by increased faecal excretion of cholesterol and bile acids. Oat bran (40%) efficiently reduced atherosclerotic lesion area in the descending aorta (-77%) and aortic root (-33%). Plasma levels of fibrinogen and soluble vascular cell adhesion molecule-1 (VCAM-1) were significantly lower, and immunofluorescence of aortic sections revealed a 75% lower expression of VCAM-1 in oat-fed mice. The expression of eNOS protein in the aortic wall was increased in mice fed oat bran. CONCLUSIONS: Oat bran supplemented to a Western diet lowers plasma cholesterol, reduces levels of some inflammatory markers, increases eNOS expression and inhibits atherosclerotic lesion development in LDLr(-/-) mice. It remains to be investigated which components in oats contribute to these effects.


Subject(s)
Anti-Inflammatory Agents/administration & dosage , Aortic Diseases/prevention & control , Atherosclerosis/prevention & control , Avena , Dietary Fiber/administration & dosage , Hypolipidemic Agents/administration & dosage , Receptors, LDL/deficiency , Animals , Aorta, Thoracic/drug effects , Aorta, Thoracic/enzymology , Aorta, Thoracic/pathology , Aortic Diseases/genetics , Aortic Diseases/metabolism , Aortic Diseases/pathology , Atherosclerosis/genetics , Atherosclerosis/metabolism , Atherosclerosis/pathology , Bile Acids and Salts/metabolism , Biomarkers/blood , Body Weight , Cholesterol/blood , Disease Models, Animal , Dose-Response Relationship, Drug , Eating , Feces/chemistry , Female , Fibrinogen/metabolism , Inflammation Mediators/blood , Lipoproteins, LDL/blood , Lipoproteins, VLDL/blood , Mice , Mice, Knockout , Nitric Oxide Synthase Type III/metabolism , Receptors, LDL/genetics , Time Factors , Triglycerides/blood , Vascular Cell Adhesion Molecule-1/blood
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