Abstract
Epilepsy is a chronic neurological disorder, and the pathophysiological progression to status epilepticus is closely associated with oxidative stress. Superoxide anions (O2•-), as the main, most important precursor of other reactive oxygen species (ROS), play a crucial role in seizure-induced brain damage. However, detecting the actual O2•- levels and understanding the physiological roles of O2• in epileptic brains remain challenging due to the lack of effective in vivo detection tools. Herein, a new near-infrared fluorescent probe, MB-SO, was prepared for the determination of endogenous O2•- in brains experiencing pentylenetetrazole (PTZ)-induced epileptic seizures. MB-SO exhibits high sensitivity (detection limit of 14 nM), good selectivity and a fast response towards O2•-. MB-SO was applied in situ to monitor endogenous O2•- in living HT-22 cells and living mice. Using this probe, we visualized and quantitatively detected endogenous O2•- for the first time in the hippocampi of PTZ-induced epileptic mouse brains. MB-SO also displayed a positive correlation between high O2•- levels in epileptic brains and epileptogenesis. These results indicated that the probe MB-SO is an efficient tool for monitoring endogenous O2•- in vivo and exploring the pathogenesis of epilepsy.
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