| Literature DB >> 25741731 |
Daniel von Bornstädt1, Thijs Houben2, Jessica L Seidel3, Yi Zheng3, Ergin Dilekoz4, Tao Qin3, Nora Sandow5, Sreekanth Kura6, Katharina Eikermann-Haerter3, Matthias Endres7, David A Boas6, Michael A Moskowitz3, Eng H Lo8, Jens P Dreier9, Johannes Woitzik5, Sava Sakadžić6, Cenk Ayata10.
Abstract
Peri-infarct depolarizations (PIDs) are seemingly spontaneous spreading depression-like waves that negatively impact tissue outcome in both experimental and human stroke. Factors triggering PIDs are unknown. Here, we show that somatosensory activation of peri-infarct cortex triggers PIDs when the activated cortex is within a critical range of ischemia. We show that the mechanism involves increased oxygen utilization within the activated cortex, worsening the supply-demand mismatch. We support the concept by clinical data showing that mismatch predisposes stroke patients to PIDs as well. Conversely, transient worsening of mismatch by episodic hypoxemia or hypotension also reproducibly triggers PIDs. Therefore, PIDs are triggered upon supply-demand mismatch transients in metastable peri-infarct hot zones due to increased demand or reduced supply. Based on the data, we propose that minimizing sensory stimulation and hypoxic or hypotensive transients in stroke and brain injury would reduce PID incidence and their adverse impact on outcome.Entities:
Mesh:
Year: 2015 PMID: 25741731 PMCID: PMC4351476 DOI: 10.1016/j.neuron.2015.02.007
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173