Key result
Chronic infusion of Urotensin II significantly increased atherosclerotic lesions within the entire aorta by 21% (P = 0.013) in cholesterol-fed rabbits compared to vehicle.
Why the study?
Does Urotensin II infusion promote atherosclerosis in cholesterol-fed rabbits?
Does Urotensin II infusion promote atherosclerosis in cholesterol-fed rabbits?
Effect estimate: 21% increase
p-value: p=0.013
Urotensin II promotes the development of atherosclerotic lesions and destabilizes plaques in a rabbit model of atherosclerosis, suggesting a potential role in cardiovascular disease pathogenesis.
Urotensin II may accelerate atherosclerosis in hypercholesterolemic rabbits; leaves open its role and therapeutic relevance in human cardiovascular disease.
Urotensin II (UII) is a vasoactive peptide composed of 11 amino acids that has been implicated to contribute to the development of cardiovascular disease. The purpose of this study was to investigate whether UII affects the development of atherosclerosis in cholesterol-fed rabbits. UII was infused for 16 weeks through an osmotic mini-pump into male Japanese White rabbits fed on a high-cholesterol diet. Plasma lipids and body weight were measured every 4 weeks. Aortic atherosclerotic lesions along with cellular components, collagen fibers, matrix metalloproteinase-1 and -9 were examined. Moreover, vulnerability index of atherosclerotic plaques was evaluated. UII infusion significantly increased atherosclerotic lesions within the entire aorta by 21% over the control (P = 0.013). Atherosclerotic lesions were increased by 24% in the aortic arch (P = 0.005), 11% in the thoracic aorta (P = 0.054) and 18% in the abdominal aorta (P = 0.035). These increases occurred without changes in plasma levels of total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides or body weight. Immunohistochemical staining revealed that macrophages and matrix metalloproteinase-9 were significantly enhanced by 2.2-fold and 1.6-fold in UII group. In vitro studies demonstrated that UII up-regulated the expression of vascular cell adhesion protein-1 and intercellular adhesion molecule-1 in human umbilical vein endothelial cells, which was inhibited by the UII receptor antagonist urantide. In conclusion, our results showed that UII promotes the development of atherosclerotic lesions and destabilizes atherosclerotic plaques in cholesterol-fed rabbits.
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Li et al. (2014) studied Atherosclerosis (n=18). Urotensin II vs. Saline (vehicle) was evaluated on Atherosclerotic lesions within the entire aorta (21% increase, p=0.013). Chronic infusion of Urotensin II significantly increased atherosclerotic lesions within the entire aorta by 21% (P = 0.013) in cholesterol-fed rabbits compared to vehicle.
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