Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, MO 63104, USA.
Arterioscler Thromb Vasc Biol. 2013 Mar;33(3):455-8. doi: 10.1161/ATVBAHA.112.300639. Epub 2013 Jan 3.
To determine the efficacy of long-term anti-miR-33 therapy on the progression of atherosclerosis in high-fat, high-cholesterol-fed Ldlr(-/-) mice.
Ldlr(-/-) mice received saline, or control or anti-miR-33 oligonucleotides once a week for 14 weeks. The treatment was effective, as measured by reduced levels of hepatic miR-33 and increased hepatic expression of miR-33 targets. Analysis of plasma samples revealed an initial elevation in high-density lipoprotein cholesterol after 2 weeks of treatment that was not sustained by the end of the experiment. Additionally, we found a significant increase in circulating triglycerides in anti-miR-33-treated mice, compared with controls. Finally, examination of atheromata revealed no significant changes in the size or composition of lesions between the 3 groups.
Prolonged silencing of miR-33 fails to maintain elevated plasma high-density lipoprotein cholesterol and does not prevent the progression of atherosclerosis in Ldlr(-/-) mice.
确定长期抗 miR-33 治疗对高脂肪、高胆固醇喂养的 Ldlr(-/-)小鼠动脉粥样硬化进展的疗效。
Ldlr(-/-)小鼠每周接受生理盐水、对照或抗 miR-33 寡核苷酸一次,共 14 周。治疗是有效的,通过降低肝 miR-33 水平和增加 miR-33 靶基因的肝表达来衡量。对血浆样本的分析显示,治疗 2 周后高密度脂蛋白胆固醇最初升高,但在实验结束时并未持续。此外,与对照组相比,抗 miR-33 处理的小鼠循环中的甘油三酯显著增加。最后,对动脉粥样瘤的检查显示,3 组之间病变的大小或组成没有显著变化。
miR-33 的长期沉默不能维持升高的血浆高密度脂蛋白胆固醇,也不能阻止 Ldlr(-/-)小鼠动脉粥样硬化的进展。