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一种基于小鼠动脉粥样硬化的新型心肌梗死模型。

A novel model of myocardial infarction based on atherosclerosis in mice.

作者信息

Wang Jianbing, Shan Shijun, Lyu Anqi, Wan Yinsheng, Zhang Jun

机构信息

Tianjin Medical University, Tianjin, China; Department of Cardiology, General Hospital of Huabei Petroleum Administration Bureau, Renqiu, Hebei, China.

Department of Dermatology, Xiang'an Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.

出版信息

Biochem Biophys Res Commun. 2021 Oct 22;576:100-107. doi: 10.1016/j.bbrc.2021.08.006. Epub 2021 Aug 31.

Abstract

RATIONALE

Coronary artery ligation to induce myocardial infarction (MI) and ischemia injury in mice is typically performed in normal mice, but This is not consistent with disease progression. There should be atherosclerosis (AS) first, followed by MI.

OBJECTIVE

We tried a novel model to induce MI that was established on atherosclerosis in mice. This approach was much more consistent with disease progression.

METHODS

In this study, Mice lacking apolipoprotein E (ApoE) were randomly divided into four groups. The mice of the control and MI groups were fed normal diet for 24-weeks, while the mice of AS and AS + MI groups were fed high-fat diet (HFD). After 23 weeks, the mice of MI and AS + MI groups were ligated with coronary arteries. A week later, after echocardiography, analysis of plaque and myocardium were conducted on aortic and heart, then the serum, aorta and heart tissues were further detected.

RESULTS

Our results showed that AS model mice exhibited significant body weight gain, dyslipidemia and atherosclerotic lesions formation which were in accordance with the pathological changes of AS. Co-treatment with AS and MI led to higher operative mortality and heart pathological were in accordance with the pathological changes of MI. In addition, Echocardiography and NT pro-BNP revealed co-treatment with AS and MI led to deterioration of cardiac function. AS also aggravated myocardial inflammatory cell infiltration and fibrosis post-MI.

CONCLUSIONS

Together, it is feasible to establish myocardial infarction model based on atherosclerosis model.

摘要

原理

在小鼠中通过冠状动脉结扎诱导心肌梗死(MI)和缺血性损伤通常在正常小鼠中进行,但这与疾病进展不一致。应该先有动脉粥样硬化(AS),然后才是MI。

目的

我们尝试了一种基于小鼠动脉粥样硬化建立的诱导MI的新模型。这种方法与疾病进展更一致。

方法

在本研究中,将缺乏载脂蛋白E(ApoE)的小鼠随机分为四组。对照组和MI组小鼠喂食正常饮食24周,而AS组和AS + MI组小鼠喂食高脂饮食(HFD)。23周后,MI组和AS + MI组小鼠进行冠状动脉结扎。一周后,在进行超声心动图检查后,对主动脉和心脏进行斑块和心肌分析,然后进一步检测血清、主动脉和心脏组织。

结果

我们的结果表明,AS模型小鼠表现出显著的体重增加、血脂异常和动脉粥样硬化病变形成,这与AS的病理变化一致。AS和MI联合处理导致更高的手术死亡率,心脏病理与MI的病理变化一致。此外,超声心动图和NT-proBNP显示AS和MI联合处理导致心脏功能恶化。AS还加重了MI后心肌炎性细胞浸润和纤维化。

结论

总之,基于动脉粥样硬化模型建立心肌梗死模型是可行的。

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