Epileptic brain fluorescent imaging reveals apigenin can relieve the myeloperoxidase-mediated oxidative stress and inhibit ferroptosis
Myeloperoxidase (MPO)-mediated oxidative stress has been suggested to play an important role in the pathological dysfunction of epileptic brains. However, there is currently no robust brainimaging tool to detect real-time endogenous hypochlorite (HClO) generation by MPO or a fluorescent probe for ra...
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Published in: | Proceedings of the National Academy of Sciences - PNAS Vol. 117; no. 19; pp. 10155 - 10164 |
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Main Authors: | , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
National Academy of Sciences
12-05-2020
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Subjects: | |
Online Access: | Get full text |
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Summary: | Myeloperoxidase (MPO)-mediated oxidative stress has been suggested to play an important role in the pathological dysfunction of epileptic brains. However, there is currently no robust brainimaging tool to detect real-time endogenous hypochlorite (HClO) generation by MPO or a fluorescent probe for rapid highthroughput screening of antiepileptic agents that control the MPO-mediated chlorination stress. Herein, we report an efficient two-photon fluorescence probe (named HCP) for the real-time detection of endogenous HClO signals generated by MPO in the brain of kainic acid (KA)-induced epileptic mice, where HClO-dependent chlorination of quinolone fluorophore gives the enhanced fluorescence response. With this probe, we visualized directly the endogenous HClO fluxes generated by the overexpression of MPO activity in vivo and ex vivo in mouse brains with epileptic behaviors. Notably, by using HCP, we have also constructed a high-throughput screening approach to rapidly screen the potential antiepileptic agents to control MPO-mediated oxidative stress. Moreover, from this screen, we identified that the flavonoid compound apigenin can relieve the MPO-mediated oxidative stress and inhibit the ferroptosis of neuronal cells. Overall, this work provides a versatile fluorescence tool for elucidating the role of HClO generation by MPO in the pathology of epileptic seizures and for rapidly discovering additional antiepileptic agents to prevent and treat epilepsy. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 1C.S. and J.Y. contributed equally to this work. Edited by Gregory A. Petsko, Brigham and Women’s Hospital, Boston, MA, and approved March 18, 2020 (received for review October 16, 2019) Author contributions: Y. Qian designed research; C.S., J.Y., Y.L., and Y. Qin performed research; J.Y., X.W., J.G., G.C., B.Z., H.-K.L., J.Z., and H.-L.Z. contributed new reagents/analytic tools; C.S., Y.L., Y. Qin, X.W., J.G., and Y. Qian analyzed data; J.Z., H.-L.Z., and Y. Qian supervised the study; and C.S. and Y. Qian wrote the paper. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.1917946117 |