Suppr超能文献

缬沙坦通过上调肾酶促进动脉粥样硬化斑块稳定:一种动脉粥样硬化潜在相关基因

Valsartan Promoting Atherosclerotic Plaque Stabilization by Upregulating Renalase: A Potential-Related Gene of Atherosclerosis.

作者信息

Zhou Mingxue, Ma Chao, Liu Weihong, Liu Hongxu, Wang Ning, Kang Qunfu, Li Ping

机构信息

Beijing Hospital of TCM Affiliated with Capital Medical University, Beijing Institute of TCM, Beijing, China Both the authors contributed equally to this work

School of Life Science, Tsinghua University, Beijing, China Both the authors contributed equally to this work.

出版信息

J Cardiovasc Pharmacol Ther. 2015 Sep;20(5):509-19. doi: 10.1177/1074248415575967. Epub 2015 Mar 27.

Abstract

BACKGROUND

Renalase is a protein that can regulate sympathetic nerve activity by metabolizing catecholamines, while redundant catecholamines are thought to contribute to atherosclerosis (As). Catecholamine release can be facilitated by angiotensin (Ang) II by binding to Ang II type 1 (AT1) receptors. Valsartan, a special AT1 antagonist, can dilate blood vessels and reduce blood pressure, but it remained unclear whether valsartan can promote the stability of atherosclerotic plaque by affecting renalase.

OBJECTIVE

This study examined the tissue distribution of renalase in ApoE(-/-) mice fed with a high-fat diet and the effect of valsartan on expression of renalase.

METHODS

ApoE(-/-) mice were fed with a high-fat diet for 13 or 26 weeks. As a control, 10 C57BL mice were fed with a standard chow diet. After 13 weeks on the high-fat diet, the ApoE(-/-) mice were randomized (10 mice/group) and treated with valsartan, simvastatin, or distilled water (control group) for an additional 13 weeks accompanied by a high-fat diet.

RESULTS

Knockout of ApoE caused a dramatic increase in expression of renalase in mice adipose tissue. With the disturbance of lipid metabolism induced by a high-fat diet, renalase expression decreased in the liver. Renalase can be expressed in smooth muscle cells and M2 macrophages in atherosclerotic plaque, and its expression gradually decreases in the fibrous cap during the transition from stable to vulnerable atherosclerotic plaque. Valsartan, an AT1 receptor antagonist, promotes the stabilization of atherosclerotic plaque by increasing the levels of renalase in serum and the expression of renalase in the fibrous cap of atherosclerotic plaque. It also reduces triglyceride levels in serum and increases the expression of renalase in the liver.

CONCLUSIONS

Renalase may be a potential-related gene of lipid metabolism and As, and it may be the possible molecular target of valsartan to help stabilize atherosclerotic plaque.

摘要

背景

肾酶是一种可通过代谢儿茶酚胺来调节交感神经活动的蛋白质,而过多的儿茶酚胺被认为会导致动脉粥样硬化(As)。血管紧张素(Ang)II与1型Ang II受体(AT1)结合可促进儿茶酚胺释放。缬沙坦是一种特殊的AT1拮抗剂,可扩张血管并降低血压,但缬沙坦是否能通过影响肾酶来促进动脉粥样硬化斑块的稳定性尚不清楚。

目的

本研究检测高脂饮食喂养的ApoE(-/-)小鼠肾酶的组织分布以及缬沙坦对肾酶表达的影响。

方法

将ApoE(-/-)小鼠高脂饮食喂养13周或26周。作为对照,10只C57BL小鼠给予标准普通饮食。高脂饮食13周后,将ApoE(-/-)小鼠随机分组(每组10只),再给予高脂饮食的同时分别用缬沙坦、辛伐他汀或蒸馏水(对照组)处理13周。

结果

敲除ApoE导致小鼠脂肪组织中肾酶表达显著增加。随着高脂饮食诱导的脂质代谢紊乱,肝脏中肾酶表达降低。肾酶可在动脉粥样硬化斑块的平滑肌细胞和M2巨噬细胞中表达,在动脉粥样硬化斑块从稳定向易损转变过程中,其在纤维帽中的表达逐渐降低。AT1受体拮抗剂缬沙坦通过提高血清肾酶水平和动脉粥样硬化斑块纤维帽中肾酶的表达来促进动脉粥样硬化斑块的稳定。它还可降低血清甘油三酯水平并增加肝脏中肾酶的表达。

结论

肾酶可能是脂质代谢和动脉粥样硬化的潜在相关基因,可能是缬沙坦帮助稳定动脉粥样硬化斑块的分子靶点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验