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Kelmanson, I.V.* ; Shokhina, A.G.* ; Kotova, D.A.* ; Pochechuev, M.S.* ; Ivanova, A.D.* ; Kostyuk, A.I.* ; Panova, A.S.* ; Borodinova, A.A.* ; Solotenkov, M.A.* ; Stepanov, E.A.* ; Raevskii, R.I.* ; Moshchenko, A.A.* ; Pak, V.V.* ; Ermakova, Y.G.* ; van Belle, G.J.C.* ; Tarabykin, V.* ; Balaban, P.M.* ; Fedotov, I.V.* ; Fedotov, A.B.* ; Conrad, M. ; Bogeski, I.* ; Katschinski, D.M.* ; Doeppner, T.R.* ; Bähr, M.* ; Zheltikov, A.M.* ; Bilan, D.S.* ; Belousov, V.V.*

In vivo dynamics of acidosis and oxidative stress in the acute phase of an ischemic stroke in a rodent model.

Redox Biol. 48:102178 (2021)
Verlagsversion DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Ischemic cerebral stroke is one of the leading causes of death and disability in humans. However, molecular processes underlying the development of this pathology remain poorly understood. There are major gaps in our understanding of metabolic changes that occur in the brain tissue during the early stages of ischemia and reperfusion. In particular, it is generally accepted that both ischemia (I) and reperfusion (R) generate reactive oxygen species (ROS) that cause oxidative stress which is one of the main drivers of the pathology, although ROS generation during I/R was never demonstrated in vivo due to the lack of suitable methods. In the present study, we record for the first time the dynamics of intracellular pH and H2O2 during I/R in cultured neurons and during experimental stroke in rats using the latest generation of genetically encoded biosensors SypHer3s and HyPer7. We detect a buildup of powerful acidosis in the brain tissue that overlaps with the ischemic core from the first seconds of pathogenesis. At the same time, no significant H2O2 generation was found in the acute phase of ischemia/reperfusion. HyPer7 oxidation in the brain was detected only 24 h later. Comparison of in vivo experiments with studies on cultured neurons under I/R demonstrates that the dynamics of metabolic processes in these models significantly differ, suggesting that a cell culture is a poor predictor of metabolic events in vivo.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Genetically Encoded Fluorescent Biosensors ; Hydrogen Peroxide ; Hypoxia/reoxygenation ; In Vivo Optical Brain Interrogation ; Ischemia/reperfusion ; Ischemic Stroke
ISSN (print) / ISBN 2213-2317
e-ISSN 2213-2317
Zeitschrift Redox Biology
Quellenangaben Band: 48, Heft: , Seiten: , Artikelnummer: 102178 Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam [u.a.]
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Metabolism and Cell Death (MCD)
Förderungen Russian Science Foundation
Ministerstwo Edukacji i Nauki