1. Protection of zero-valent iron nanoparticles against sepsis and septic heart failure
- Author
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Daquan, Wang, Changyu, Wang, Zhenxing, Liang, Wangrui, Lei, Chao, Deng, Xiaoli, Liu, Shuai, Jiang, Yanli, Zhu, Shaofei, Zhang, Wenwen, Yang, Ying, Chen, Yao, Qiu, Lingjie, Meng, and Yang, Yang
- Subjects
Heart Failure ,Iron ,Myocardium ,Biomedical Engineering ,Pharmaceutical Science ,Medicine (miscellaneous) ,Bioengineering ,Applied Microbiology and Biotechnology ,Mice ,Heart Injuries ,Sepsis ,Animals ,Nanoparticles ,Molecular Medicine - Abstract
Background Septic heart failure accounts for high mortality rates globally. With a strong reducing capacity, zero-valent iron nanoparticles (nanoFe) have been applied in many fields. However, the precise roles and mechanisms of nanoFe in septic cardiomyopathy remain unknown. Results NanoFe was prepared via the liquid-phase reduction method and functionalized with the biocompatible polymer sodium carboxymethylcellulose (CMC). We then successfully constructed a mouse model of septic myocardial injury by challenging with cecal ligation and puncture (CLP). Our findings demonstrated that nanoFe has a significant protective effect on CLP-induced septic myocardial injury. This may be achieved by attenuating inflammation and oxidative stress, improving mitochondrial function, regulating endoplasmic reticulum stress, and activating the AMPK pathway. The RNA-seq results supported the role of nanoFe treatment in regulating a transcriptional profile consistent with its role in response to sepsis. Conclusions The results provide a theoretical basis for the application strategy and combination of nanoFe in sepsis and septic myocardial injury. Graphical Abstract
- Published
- 2022
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