The combination of Fucus vesiculosus-derived fucoidan and simvastatin attenuates atherosclerosis induced by a high-fat diet plus balloon catheter injury in New Zealand rabbits.

Although statins reduce cardiovascular disease (CVD) events by approximately 30 %, additional effective therapeutic strategies are necessary. This investigation examined the anti-atherosclerotic effects of Fucus vesiculosus-derived fucoidan (F), independently and in combination with simvastatin (SV), in New Zealand rabbits with atherosclerosis induced by a high-fat diet and balloon catheter injury, a model that effectively replicates human atherosclerosis pathology. The findings demonstrated that fucoidan administration substantially decreased plasma total cholesterol (TC) and triglyceride (TG) levels by >10.0 % and 50.0 %, respectively. Notably, FSV combination therapy achieved enhanced lipid-lowering effects and decreased plasma TC and TG by 28.9 % and 89.3 %. Consistently, fucoidan intervention groups showed decreased abdominal lesion/lm ratio by >36.6 %; and the FSV group further reduced this value by 22.7 % compared to that achieved by SV monotherapy. Mechanistically, the combination therapy increased the expression of PPARs, LXRα, and downstream lipid transporters in the aorta. It enhanced the expression of LDLR, PPARα, and HSL and LXRα/ABCG5 signaling and suppressed PGC1β in the liver. The combined therapy reduced NPC1L1 expression and enhanced LXRα/ABCG5 signaling in the small intestine. These results indicate that FSV combination therapy is a promising approach for the prevention of atherosclerotic CVD, thus promoting their potential clinical translation.