血管内皮细胞参与利拉鲁肽对糖尿病载脂蛋白e缺失小鼠的抗动脉粥样硬化作用

M. Koshibu, Y. Mori, Hideki Kushima, Munenori Hiromura, Kyoko Kohashi, Michishige Terasaki, Naoya Osaka, Tomoki Fujikawa, Tomoyasu Fukui, T. Hirano
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引用次数: 0

摘要

胰高血糖素样肽1受体激动剂(GLP-1RAs)已被证明通过多种机制对不同类型的细胞发挥抗动脉粥样硬化作用。然而,目前尚不清楚这些机制中哪一个是至关重要的。我们在小鼠动脉粥样硬化模型中研究了血管内皮细胞(VECs)在GLP-1RA利拉鲁肽抗动脉粥样硬化作用中的作用。随机分为两组,一组用生理盐水治疗,另一组用利拉鲁肽(107 nmol/kg/天)治疗,并进行股动脉钢丝损伤以去除VECs。血糖> 300血红蛋白A1c水平> 9%,表明已诱导严重高血糖。观察斑块与斑块之间的胆固醇和甘油三酯;然而,严重的斑块形成发生在因插入金属丝去除vec而受伤的股动脉中。与未损伤主动脉不同,利拉鲁肽治疗不影响导线损伤股动脉的斑块体积或动脉重塑(内膜和内侧变薄以及动脉扩张)。在利拉鲁肽影响的各种细胞中,VECs在利拉鲁肽对糖尿病小鼠的抗动脉粥样硬化作用中起核心作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Involvement of Vascular Endothelial Cells in the Anti-atherogenic Effects of Liraglutide in Diabetic Apolipoprotein E-null Mice
: Glucagon-like peptide 1 receptor agonists ( GLP-1RAs ) have been shown to exert anti-atherosclerotic effects via multiple mechanisms on different types of cells. However, it is unclear which of these mechanisms are crucial. We investigated the role of vascular endothelial cells ( VECs ) in the anti-atherogenic effects of the GLP-1RA liraglutide in a mouse model of atherosclerosis. were randomly assigned to treatment with either vehicle ( saline ) or liraglutide ( 107 nmol/kg/day ) , and were subjected to femoral artery wire injury to remove VECs. glucose > 300 hemoglobin A1c levels of > 9 % , indicating the had induced severe hyperglycemia. cholesterol, and triglycerides between the and plaques were observed ; however, severe plaque formation occurred in femoral arteries that had been injured by wire insertion to remove VECs. Unlike in the uninjured aorta, liraglutide treatment did not affect plaque volume or arterial remodeling ( intimal and medial thinning, and arterial dilation ) in wire-injured femoral arteries. Of the various cells that liraglutide affects, VECs play a central role in liraglutide ʼ s anti-atherogenic effects in diabetic mice.
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