Dietary α-linolenic acid delayed arterial thrombus formation in mice compared with a low-ALA diet (P<0.005) and inhibited tissue factor expression and platelet activation.
Does dietary α-linolenic acid reduce arterial thrombus formation and platelet activation in preclinical models?
Dietary α-linolenic acid demonstrates direct antithrombotic effects by impairing arterial thrombus formation, tissue factor expression, and platelet activation in preclinical models.
p-value: p=<0.005
OBJECTIVE: Plant-derived α-linolenic acid (ALA) may constitute an attractive cardioprotective alternative to fish-derived n-3 fatty acids. However, the effect of dietary ALA on arterial thrombus formation remains unknown. METHODS AND RESULTS: Male C57Bl/6 mice were fed a high-ALA or low-ALA diet for 2 weeks. Arterial thrombus formation was delayed in mice fed a high-ALA diet compared with those on a low-ALA diet (n=7; P<0.005). Dietary ALA impaired platelet aggregation to collagen and thrombin (n=5; P<0.005) and decreased p38 mitogen-activated protein kinase activation in platelets. Dietary ALA impaired arterial tissue factor (TF) expression, TF activity, and nuclear factor-κB activity (n=7; P<0.05); plasma clotting times and plasma thrombin generation did not differ (n=5; P=not significant). In cultured human vascular smooth muscle and endothelial cells, ALA inhibited TF expression and activity (n=4; P<0.01). Inhibition of TF expression occurred at the transcriptional level via the mitogen-activated protein kinase p38 in smooth muscle cells and p38, extracellular signal-regulated kinases 1 and 2, and c-Jun N-terminal kinases 1 and 2 in endothelial cells. CONCLUSIONS: ALA impairs arterial thrombus formation, TF expression, and platelet activation and thereby represents an attractive nutritional intervention with direct dual antithrombotic effects.
Holy et al. (2011) studied Arterial thrombus formation. Dietary α-Linolenic Acid (high-ALA diet) vs. Low-ALA diet was evaluated on Arterial thrombus formation (p=<0.005). Dietary α-linolenic acid delayed arterial thrombus formation in mice compared with a low-ALA diet (P<0.005) and inhibited tissue factor expression and platelet activation.
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