Peri-Infarct Hot-Zones Have Higher Susceptibility to Optogenetic Functional Activation-Induced Spreading Depolarizations
Author(s) -
Kazutaka Sugimoto,
David Y. Chung,
Maximilian Böhm,
Paul Fischer,
Tsubasa Takizawa,
Sanem A Aykan,
Tao Qin,
Takeshi Yanagisawa,
Andrea M. Harriott,
Fumiaki Oka,
Mohammad A. Yaseen,
Sava Sakadžić,
Cenk Ayata
Publication year - 2020
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.120.029618
Subject(s) - optogenetics , medicine , somatosensory system , stimulation , perfusion , depolarization , stroke (engine) , cardiology , infarction , stroke recovery , neuroscience , myocardial infarction , biology , mechanical engineering , psychiatry , rehabilitation , physical therapy , engineering
Background and Purpose: Spreading depolarizations (SDs) are recurrent and ostensibly spontaneous depolarization waves that may contribute to infarct progression after stroke. Somatosensory activation of the metastable peri-infarct tissue triggers peri-infarct SDs at a high rate. Methods: We directly measured the functional activation threshold to trigger SDs in peri-infarct hot zones using optogenetic stimulation after distal middle cerebral artery occlusion in Thy1-ChR2-YFP mice. Results: Optogenetic activation of peri-infarct tissue triggered SDs at a strikingly high rate (64%) compared with contralateral homotopic cortex (8%;P =0.004). Laser speckle perfusion imaging identified a residual blood flow of 31±2% of baseline marking the metastable tissue with a propensity to develop SDs.Conclusions: Our data reveal a spatially distinct increase in SD susceptibility in peri-infarct tissue where physiological levels of functional activation are capable of triggering SDs. Given the potentially deleterious effects of peri-infarct SDs, the effect of sensory overstimulation in hyperacute stroke should be examined more carefully.
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