Key result
Olmesartan medoxomil effectively reduced atherosclerotic lesion surface area and thickness in ApoEKO mice, demonstrating that its antiatherosclerotic effect is not weakened by severe hyperlipidemia.
Why the study?
Does olmesartan medoxomil reduce atherosclerotic lesions in ApoEKO mice regardless of hyperlipidemia severity?
Does olmesartan medoxomil reduce atherosclerotic lesions in ApoEKO mice regardless of hyperlipidemia severity?
Olmesartan medoxomil exerts antiatherosclerotic effects in a mouse model regardless of the severity of hyperlipidemia, suggesting potential benefits even when cholesterol is not fully controlled.
Animal data leave open clinical translation of olmesartan’s antiatherosclerotic effects; hypothesis-generating only.
The purpose of this study was to clarify whether severity of hyperlipidemia affects the antiatherosclerotic effect of angiotensin II receptor blockers (ARBs). The effect of olmesartan medoxomil, an ARB, on atherosclerotic lesion was examined in apolipoprotein E-deficient (ApoEKO) mice fed a normal diet (ND) or a high-fat-supplemented diet (FD) for 25 weeks. ApoEKO mice have high plasma cholesterol levels, which were further increased by feeding of an FD. Both the atherosclerotic lesion area of the aortic luminal surface and the atherosclerotic lesion thickness in the aortic valves were significantly greater in the FD mice than in the ND mice. Olmesartan medoxomil did not affect the plasma cholesterol levels in either the ND or FD ApoEKO mice; however, it reduced effectively both the atherosclerotic lesion surface area and the lesion thickness even in FD ApoEKO mice. It is concluded that the antiatherosclerotic effect of ARBs is not weakened by the high plasma cholesterol level, suggesting the usefulness of ARBs in the treatment of atherosclerosis, even in a situation in which the plasma cholesterol level is not fully controlled.
No takes yet. Share an insight, caveat, or question.
Kato et al. (2006) studied Atherosclerosis and Hyperlipidemia. Olmesartan medoxomil vs. Control (no ARB) was evaluated on Atherosclerotic lesion area of the aortic luminal surface and lesion thickness in the aortic valves. Olmesartan medoxomil effectively reduced atherosclerotic lesion surface area and thickness in ApoEKO mice, demonstrating that its antiatherosclerotic effect is not weakened by severe hyperlipidemia.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: