Mitochondrial Peroxynitrite Mediation of Anthracycline-Induced Cardiotoxicity as Visualized by a Two-Photon Near-Infrared Fluorescent Probe

被引:114
作者
Xie, Xilei [1 ]
Tang, Fuyan [1 ]
Liu, Guangzhao [1 ]
Li, Yong [1 ]
Su, Xingxing [1 ]
Jiao, Xiaoyun [1 ]
Wang, Xu [1 ]
Tang, Bo [1 ]
机构
[1] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Collaborat Innovat Ctr Functionalized Probes Chem, Key Lab Mol & Nano Probes,Minist Educ,Inst Mol &, Jinan 250014, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
AGGREGATION-INDUCED EMISSION; DRUG-INDUCED HEPATOTOXICITY; IN-VIVO; NITRIC-OXIDE; LIVE CELLS; ENDOGENOUS PEROXYNITRITE; BIOLOGICAL APPLICATIONS; ANTICANCER TREATMENTS; SELECTIVE DETECTION; HYDROGEN-PEROXIDE;
D O I
10.1021/acs.analchem.8b03207
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Anthracyclines rank among the most efficacious anticancer medications. However, their clinical utility and oncologic efficacy are severely compromised by the cardiotoxicity risk facing the early-diagnosis difficulty and their unclear molecular mechanism. Herein, a two-photon-excitable and near-infrared-emissive fluorescent probe, TPNIR-FP, was fabricated and endowed with extraordinary specificity and sensitivity and a rapid response toward peroxynitrite (ONOO-), as well as mitochondria-targeting ability. With the aid of TPNIR-FP, we demonstrate that mitochondrial ONOO- is upregulated in the early stage and contributes to the onset and progression of anthracycline cardiotoxicity in cardiomyocyte and mouse models; therefore, it represents an early biomarker to predict subclinical cardiotoxicity induced by drug challenge. Furthermore, TPNIR-FP is proved to be a robust imaging tool to provide critical insights into drug-induced cardiotoxicity and other ONOO- related pathophysiological processes.
引用
收藏
页码:11629 / 11635
页数:7
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