TY - JOUR
T1 - Inhalation metal-phenolic nanozyme as a novel therapeutic strategy for lung ischemia-reperfusion injury
AU - Sun, Shirui
AU - Ren, Kaixiang
AU - He, Bin
AU - Zhao, Yilong
AU - Jiang, Rongxuan
AU - Zhu, Xingzhuo
AU - Dong, Niuniu
AU - Guo, Yingcong
AU - He, Qi
AU - Huang, Jiahao
AU - Ding, Chenguang
AU - Yang, Mei
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2026/3
Y1 - 2026/3
N2 - Background Lung ischemia-reperfusion injury (LIRI) is a complex pathophysiological process with few existing therapeutic options. New drugs are needed to target both oxidative stress and enhanced sterile inflammation during ischemia-reperfusion. Results In this study, we developed a metal-phenolic nanozyme (Cur-Fe) that possesses significant enzyme-like activities, including superoxide dismutase (SOD)-like activity and hydroxyl radical (•OH) scavenging ability, and can effectively modulate inflammatory cytokines and maintain cellular homeostasis in vitro . In the mouse LIRI model, nebulized inhalation of Cur-Fe nanozyme significantly reduced lung inflammation and oxidative stress, improved lung tissue function, and restored alveolar structure. It is important to note that transcriptomics and metabolomics analyses demonstrated that Cur-Fe nanozyme modulated key metabolic pathways, including the cGMP-PKG signaling pathway and amino acid metabolism, thereby promoting its protective effects on lung tissue. Conclusion In this study, we present a Cur-Fe nanozyme that shows great potential in mitigating LIRI-associated lung injury by targeting oxidative stress and inflammation as well as regulating key transcriptional and metabolic pathways. This innovative approach provides a new avenue for the development of nanomedicines for the treatment of ischemia-reperfusion-related diseases with promising clinical applications.
AB - Background Lung ischemia-reperfusion injury (LIRI) is a complex pathophysiological process with few existing therapeutic options. New drugs are needed to target both oxidative stress and enhanced sterile inflammation during ischemia-reperfusion. Results In this study, we developed a metal-phenolic nanozyme (Cur-Fe) that possesses significant enzyme-like activities, including superoxide dismutase (SOD)-like activity and hydroxyl radical (•OH) scavenging ability, and can effectively modulate inflammatory cytokines and maintain cellular homeostasis in vitro . In the mouse LIRI model, nebulized inhalation of Cur-Fe nanozyme significantly reduced lung inflammation and oxidative stress, improved lung tissue function, and restored alveolar structure. It is important to note that transcriptomics and metabolomics analyses demonstrated that Cur-Fe nanozyme modulated key metabolic pathways, including the cGMP-PKG signaling pathway and amino acid metabolism, thereby promoting its protective effects on lung tissue. Conclusion In this study, we present a Cur-Fe nanozyme that shows great potential in mitigating LIRI-associated lung injury by targeting oxidative stress and inflammation as well as regulating key transcriptional and metabolic pathways. This innovative approach provides a new avenue for the development of nanomedicines for the treatment of ischemia-reperfusion-related diseases with promising clinical applications.
KW - Inflammation
KW - Inhalation
KW - Lung ischemia-reperfusion injury
KW - Metal-phenolic nanozyme
KW - Oxidative stress
UR - https://www.scopus.com/pages/publications/105044392821
U2 - 10.1016/j.bioadv.2025.214558
DO - 10.1016/j.bioadv.2025.214558
M3 - 文章
C2 - 41110301
AN - SCOPUS:105044392821
SN - 2772-9508
VL - 180
JO - Biomaterials Advances
JF - Biomaterials Advances
M1 - 214558
ER -