姜黄素
活性氧
急性肾损伤
抗氧化剂
超氧化物歧化酶
氧化应激
PEG比率
化学
细胞凋亡
聚乙二醇
药理学
医学
生物化学
内科学
财务
经济
作者
Xinyu Huang,Fengxian Zhang,Yuan Yang,Jiawei Liu,Xiangyun Tan,Peng Zhou,Xiaolei Tang,Junjie Hu,Liang Chen,Ming Yuan,Guohua Zheng,Ziqiang Xu,Zhenpeng Qiu
标识
DOI:10.1016/j.mtbio.2025.101794
摘要
Acute kidney injury (AKI) is a heterogeneous disorder frequently occurring in hospitalized patients with multiple comorbidities. Chemotherapy-associated AKI (e.g., cisplatin-induced AKI, CP-AKI) and rhabdomyolysis-induced AKI (RM-AKI) are initiated by the excessive accumulation of reactive oxygen species (ROS). Herein, metal phenolic networks (MPNs) composed of copper (II) (Cu2+), a typical cofactor in the native superoxide dismutase (SOD), and a well-studied natural antioxidant curcumin (Cur) (denoted as Cur-Cu) were fabricated to integrate the ROS-scavenging properties of metal ions and polyphenols. The results indicate that Cur-Cu nanoparticles (NPs) possessed robust antioxidative enzyme-like activities. Meanwhile, Cur-Cu NPs with polyethylene glycol (PEG) covalent modification (Cur-Cu@PEG) abolished the ROS-triggered oxidative damage of HK-2 cells. Moreover, Cur-Cu@PEG displayed acceptable biocompatibility in vivo. Furthermore, Cur-Cu@PEG alleviated CP-AKI and RM-AKI in mice with kidney-targeted delivery. Mechanistically, Cur-Cu@PEG effectively lessened the production of ROS, thereby repressing caspase-3-dependent apoptotic/pyroptotic cell death in the kidneys of AKI mice. Altogether, these results offer a viable approach for synthesizing antioxidant metal phenolic networks mimics to ameliorate ROS-related diseases.
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