Novel gold-platinum nanoparticles serve as broad-spectrum antioxidants for attenuating ischemia reperfusion injury of the kidney

被引:23
|
作者
Feng, Shijian [1 ,2 ,3 ,4 ,5 ]
Qu, Ying [1 ,2 ,3 ,4 ]
Chu, Bingyang [1 ,2 ,3 ,4 ]
Chen, Xiaoting [6 ]
Yang, Ziyan [7 ]
Li, Peiwen [7 ]
Wang, Peiyu [7 ]
He, Qiyu [1 ,2 ,3 ,4 ]
He, Yushi [1 ,2 ,3 ,4 ]
Lin, Tao [1 ,2 ,3 ,4 ,5 ]
Huang, Zhongli [1 ,2 ,3 ,4 ,5 ,8 ]
Qian, Zhiyong [1 ,2 ,3 ,4 ,8 ]
机构
[1] Sichuan Univ, Dept Urol, Chengdu, Peoples R China
[2] Inst Urol, Dept Hematol, Lab Reconstruct Urol, Sichuan, Peoples R China
[3] State Key Lab Biotherapy, Inst Hematol, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp, Canc Ctr, Peoples Republ, Chengdu, Peoples R China
[5] Sichuan Univ, West China Hosp, Organ Transplantat Ctr, Chengdu, Peoples R China
[6] Sichuan Univ, West China Hosp, Anim Expt Ctr, Chengdu, Peoples R China
[7] Sichuan Univ, West China Sch Clin Med, Chengdu, Peoples R China
[8] 37 Guoxue Alley, Wuhou Dist, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
AuPt nanoparticles; kidney ischemia-reperfusion injury; ROS scavenging; INFLAMMATION; PEROXIDASE;
D O I
10.1016/j.kint.2022.07.004
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Kidney ischemia reperfusion injury (IRI) is a common and inevitable pathological condition in routine urological practices, especially during transplantation. Severe kidney IRI may even induce systemic damage to peripheral organs, and lead to multisystem organ failure. However, no standard clinical treatment option is currently available. It has been reported that kidney IRI is predominantly associated with abnormally increased endogenous reactive oxygen species (ROS). Scavenging excessive ROS may reduce the damage caused by oxidative stress and subsequently alleviate kidney IRI. Here, we reported a simple and efficient one-step synthesis of gold-platinum nanoparticles (AuPt NPs) with a gold core having a loose and branched outer platinum shell with superior ROS scavenging capacity to possibly treat kidney IRI. These AuPt NPs exhibited multiple enzyme-like anti-oxidative properties simultaneously possessing catalase-and peroxidase-like activity. These particles showed excellent cell protective capability, and alleviated kidney IRI both in vitro and in vivo without obvious toxicity, by suppressing cell apoptosis, inflammatory cytokine release, and inflammasome formation. Meanwhile, AuPt NPs also had an effect on inhibiting the transition to chronic kidney disease by reducing kidney fibrosis in the long term. Thus, AuPt NPs might be a good therapeutic agent for kidney IRI management and may be helpful for the development of clinical treatments for kidney IRI.
引用
收藏
页码:1057 / 1072
页数:16
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