化学
过氧化氢
线粒体
缺血
体内
渗透(战争)
生物物理学
药理学
生物化学
内科学
生物技术
医学
生物
运筹学
工程类
作者
Cong Fang,Quan Deng,Kuicheng Zhao,Zile Zhou,Xiaohua Zhu,Feng Liu,Peng Yin,Meiling Liu,Haitao Li,Youyu Zhang,Shouzhuo Yao
标识
DOI:10.1021/acs.analchem.3c04781
摘要
Cerebral ischemia–reperfusion injury (CIRI), a cause of cerebral dysfunction during cerebral infarction treatment, is closely associated with mitochondrial viscosity and hydrogen peroxide (H2O2). However, the accurate measurement of mitochondrial viscosity and H2O2 levels in CIRI is challenging because of the lack of sufficient selectivity and blood–brain barrier (BBB) penetration of existing monitoring tools related to CIRI, hampering the exploration of the role of mitochondrial viscosity and H2O2 in CIRI. To address this issue, we designed an activatable fluorescent probe, mitochondria-targeting styryl-quinolin-ium (Mito-IQS), with excellent properties including high selectivity, mitochondrial targeting, and BBB penetration, for the visualization of mitochondrial viscosity and H2O2 in the brain. Based on the real-time monitoring capabilities of the probe, bursts of mitochondrial viscosity and H2O2 levels were visualized during CIRI. This probe can be used to monitor the therapeutic effects of butylphthalein treatment. More importantly, in vivo experiments further confirmed that CIRI was closely associated with the mitochondrial viscosity and H2O2 levels. This discovery provides new insights and tools for the study of CIRI and is expected to accelerate the process of CIRI diagnosis, treatment, and drug design.
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