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神经调节蛋白-1基因转导对心肌梗死大鼠的治疗作用。

Therapeutic effects of neuregulin-1 gene transduction in rats with myocardial infarction.

作者信息

Xiao Jian, Li Bingong, Zheng Zeqi, Wang Menghong, Peng Jingtian, Li Yong, Li Zhe

机构信息

Hypertensive Research Institute, First Affiliated Hospital, Nanchang University, Nanchang, China.

出版信息

Coron Artery Dis. 2012 Nov;23(7):460-8. doi: 10.1097/MCA.0b013e32835877da.

Abstract

AIM

In this study, we investigated whether lentivirus-mediated gene transduction improves the cardiac function in rats with myocardial infarction and the mechanisms involved.

METHODS AND RESULTS

Briefly, lentivirus carrying human neuregulin-1 (hNRG-1) gene was injected into infarcted myocardium of rats. Four weeks later, lentivirus-mediated gene transduction promoted hNRG-1 gene and protein expression. Overexpression of hNRG-1 increased the number of microvessels in the ischemic myocardium and decreased the number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)-stained positive cells. Furthermore, qRT-PCR assay showed that hNRG-1 was capable of increasing the expression of bcl-2 and VEGF-A while decreasing the expression of bax. Western blot analysis suggested that overexpression of hNRG-1 activated the PI3K/Akt pathway and increased the phosphorylation of Akt and eNOS.

CONCLUSION

These findings suggest that NRG-1 gene transduction can improve cardiac function by promoting angiogenesis and preventing apoptosis.

摘要

目的

在本研究中,我们探究了慢病毒介导的基因转导是否能改善心肌梗死大鼠的心脏功能及其相关机制。

方法与结果

简要来说,将携带人神经调节蛋白-1(hNRG-1)基因的慢病毒注射到大鼠梗死心肌中。四周后,慢病毒介导的基因转导促进了hNRG-1基因和蛋白表达。hNRG-1的过表达增加了缺血心肌中的微血管数量,并减少了末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)染色阳性细胞的数量。此外,qRT-PCR分析表明,hNRG-1能够增加bcl-2和VEGF-A的表达,同时降低bax的表达。蛋白质印迹分析表明,hNRG-1的过表达激活了PI3K/Akt通路,并增加了Akt和eNOS的磷酸化。

结论

这些发现表明,NRG-1基因转导可通过促进血管生成和防止细胞凋亡来改善心脏功能。

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