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Long-term dietary n3 fatty acid prevents aging-related cardiac diastolic and vascular dysfunction

医学 内科学 射血分数 心力衰竭 舒张期 纤维化 心脏病学 内皮功能障碍 内分泌学 射血分数保留的心力衰竭 炎症 利钠肽 血压
作者
Seyed Soheil Saeedi Saravi,Nicole R. Bonetti,Ana Vukolic,Daria Vdovenko,Pratintip Lee,Luca Liberale,Cristina Basso,Stefania Rizzo,Alexander Akhmedov,Thomas F. Lüscher,Giovanni G. Camici,Jürg Beer
出处
期刊:Vascular Pharmacology [Elsevier]
卷期号:150: 107175-107175 被引量:5
标识
DOI:10.1016/j.vph.2023.107175
摘要

The prevalence of left ventricular (LV) diastolic and vascular dysfunction increases with age, eventually leading to heart failure with preserved ejection fraction (HFpEF). A preventive strategy is an unmet medical need. We and others reported previously on the beneficial effects of omega-3 fatty acid alpha linolenic acid (ALA) on cardiovascular disorders in animal models and translational studies. We now investigate whether long-term dietary ALA could prevent LV diastolic dysfunction and vascular aging in a murine model.Wild-type C57BL/6 J mice were fed a chow or ALA diet for 12 months, starting at 6 months of age. Here, we show that aged (~18 months) mice recapitulate major hallmarks of HFpEF, including LV diastolic dysfunction with preserved ejection fraction, impaired vascular function, cardiac fibrosis, arterial stiffening and inflammation, as well as elevated B-type natriuretic peptide (BNP). Long-term ALA supplementation upregulated the mitochondrial tricarboxylic acid enzyme Idh2 and the antioxidant enzymes SOD1 and Gpx1. It also has been associated with reduced inflammation and ECM remodeling, accompanied by a significant downregulation of fibrosis biomarkers MMP-2 and TGF-β in both cardiac and vascular tissues obtained from aged mice. Our data exhibited the preventive effects of dietary ALA against LV diastolic dysfunction, impaired vasorelaxation, cardiac fibrosis, inflammation and arterial stiffening in aged mice.We provide evidence and a simplified mechanistic insight on how long-term ALA supplementation is a successful strategy to prevent the development of age-related diastolic and vascular dysfunction.
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