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美托洛尔可降低载脂蛋白E基因敲除(ApoE-/-)小鼠体内的促炎细胞因子水平并减轻动脉粥样硬化。

Metoprolol reduces proinflammatory cytokines and atherosclerosis in ApoE-/- mice.

作者信息

Ulleryd Marcus A, Bernberg Evelina, Yang Li Jin, Bergström Göran M L, Johansson Maria E

机构信息

Department of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, P.O. Box 432, 405 30 Gothenburg, Sweden.

The Wallenberg Laboratory, Department of Molecular and Clinical Medicine/Clinical Physiology, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden.

出版信息

Biomed Res Int. 2014;2014:548783. doi: 10.1155/2014/548783. Epub 2014 Jul 8.

Abstract

A few studies in animals and humans suggest that metoprolol (β1-selective adrenoceptor antagonist) may have a direct antiatherosclerotic effect. However, the mechanism behind this protective effect has not been established. The aim of the present study was to evaluate the effect of metoprolol on development of atherosclerosis in ApoE(-/-) mice and investigate its effect on the release of proinflammatory cytokines. Male ApoE(-/-) mice were treated with metoprolol (2.5 mg/kg/h) or saline for 11 weeks via osmotic minipumps. Atherosclerosis was assessed in thoracic aorta and aortic root. Total cholesterol levels and Th1/Th2 cytokines were analyzed in serum and macrophage content in lesions by immunohistochemistry. Metoprolol significantly reduced atherosclerotic plaque area in thoracic aorta (P < 0.05 versus Control). Further, metoprolol reduced serum TNFα and the chemokine CXCL1 (P < 0.01 versus Control for both) as well as decreasing the macrophage content in the plaques (P < 0.01 versus Control). Total cholesterol levels were not affected. In this study we found that a moderate dose of metoprolol significantly reduced atherosclerotic plaque area in thoracic aorta of ApoE(-/-) mice. Metoprolol also decreased serum levels of proinflammatory cytokines TNFα and CXCL1 and macrophage content in the plaques, showing that metoprolol has an anti-inflammatory effect.

摘要

一些在动物和人类身上进行的研究表明,美托洛尔(β1选择性肾上腺素能受体拮抗剂)可能具有直接的抗动脉粥样硬化作用。然而,这种保护作用背后的机制尚未明确。本研究的目的是评估美托洛尔对ApoE(-/-)小鼠动脉粥样硬化发展的影响,并研究其对促炎细胞因子释放的作用。雄性ApoE(-/-)小鼠通过渗透微型泵接受美托洛尔(2.5毫克/千克/小时)或生理盐水治疗11周。对胸主动脉和主动脉根部的动脉粥样硬化情况进行评估。通过免疫组织化学分析血清中的总胆固醇水平以及病变中的Th1/Th2细胞因子和巨噬细胞含量。美托洛尔显著降低了胸主动脉的动脉粥样硬化斑块面积(与对照组相比,P < 0.05)。此外,美托洛尔降低了血清TNFα和趋化因子CXCL1(两者与对照组相比,P < 0.01),同时减少了斑块中的巨噬细胞含量(与对照组相比,P < 0.01)。总胆固醇水平未受影响。在本研究中,我们发现中等剂量的美托洛尔显著降低了ApoE(-/-)小鼠胸主动脉的动脉粥样硬化斑块面积。美托洛尔还降低了血清中促炎细胞因子TNFα和CXCL1的水平以及斑块中的巨噬细胞含量,表明美托洛尔具有抗炎作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8094/4109227/f305e34fa4a1/BMRI2014-548783.001.jpg

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