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依折麦布通过抑制炎症来预防肥胖大鼠模型中的心肌重塑。

Ezetimibe prevents myocardial remodeling in an obese rat model by inhibiting inflammation.

作者信息

Li Xiao-Xing, Zhao Lang, Chang Ying, Liu Bao-Shan, Xu Feng, Zhang Cheng, Ji Xiao-Ping, Chen Yu-Guo, Li Chuan-Bao

机构信息

Department of Geriatrics, Qilu Hospital, Shandong University Jinan, Shandong, China.

Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Public Health, Qilu Hospital, Shandong University, Jinan, Shandong, China.

出版信息

Acta Biochim Pol. 2018;65(3):465-470. doi: 10.18388/abp.2018_2597. Epub 2018 Sep 8.

Abstract

Inflammation plays an important role in the development of many obesity-related diseases. This study aimed to investigate the effect of ezetimibe on inflammation and myocardial remodeling in obese rats. A rat model of obesity was established, and myocardial damage was examined by transmission electron microscopy and Masson staining. Twenty obese rats were divided into two groups (n=10): obese group and ezetimibe group. Ten SD rats were used as controls. Western blot was performed to monitor the expression of P-p38MAPK and interleukin (IL)-6. Immunohistochemical staining was used to monitor the expression of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1. In the obese rats group, we observed increased inflammatory factors and myocardial hypertrophy. In contrast, the ezetimibe group exhibited decreased expression of inflammatory factors and an improvement in myocardial remodeling compared to the obese group. Mechanistically, we found that ezetimibe decreased P-p38MAPK, IL-6, intercellular adhesion molecule-1, and vascular cell adhesion molecule-1 levels in the hearts of the obese rats. Taken together, these results indicate that ezetimibe may improve myocardial remodeling in obese rats by inhibiting inflammation.

摘要

炎症在许多肥胖相关疾病的发展中起着重要作用。本研究旨在探讨依泽替米贝对肥胖大鼠炎症和心肌重塑的影响。建立肥胖大鼠模型,通过透射电子显微镜和Masson染色检测心肌损伤。将20只肥胖大鼠分为两组(n = 10):肥胖组和依泽替米贝组。10只SD大鼠作为对照组。采用蛋白质免疫印迹法监测P-p38MAPK和白细胞介素(IL)-6的表达。采用免疫组织化学染色法监测细胞间黏附分子-1和血管细胞黏附分子-1的表达。在肥胖大鼠组中,我们观察到炎症因子增加和心肌肥大。相比之下,与肥胖组相比,依泽替米贝组炎症因子表达降低,心肌重塑得到改善。从机制上讲,我们发现依泽替米贝降低了肥胖大鼠心脏中P-p38MAPK、IL-6、细胞间黏附分子-1和血管细胞黏附分子-1的水平。综上所述,这些结果表明依泽替米贝可能通过抑制炎症来改善肥胖大鼠的心肌重塑。

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