Synaptic Zn 2+ contributes to deleterious consequences of spreading depolarizations

Spreading depolarizations (SDs) are profound waves of neuroglial depolarization that can propagate repetitively through injured brain. Recent clinical work has established SD as an important contributor to expansion of acute brain injuries and have begun to extend SD studies into other neurological...

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Bibliographic Details
Published inNeurobiology of disease Vol. 191; p. 106407
Main Authors Bennett, Michael C, Reinhart, Katelyn M, Weisend, Jordan E, Morton, Russell A, Carlson, Andrew P, Shuttleworth, C William
Format Journal Article
LanguageEnglish
Published United States 01.02.2024
Subjects
Animals
Chelating Agents
Cortical Spreading Depression
Hippocampus - metabolism
Membrane Transport Proteins
Mice
Neuroglia - metabolism
Zinc - metabolism
Ischemia
hippocampus
ZnT3
Spreading depression
Zinc
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Summary:Spreading depolarizations (SDs) are profound waves of neuroglial depolarization that can propagate repetitively through injured brain. Recent clinical work has established SD as an important contributor to expansion of acute brain injuries and have begun to extend SD studies into other neurological disorders. A critical challenge is to determine how to selectively prevent deleterious consequences of SD. In the present study, we determined whether a wave of profound Zn release is a key contributor to deleterious consequences of SD, and whether this can be targeted pharmacologically. Focal KCl microinjection was used to initiate SD in the CA1 region of the hippocampus in murine brain slices. An extracellular Zn chelator with rapid kinetics (ZX1) increased SD propagation rates and improved recovery of extracellular DC potential shifts. Under conditions of metabolic compromise, tissues showed sustained impairment of functional and structural recovery following a single SD. ZX1 effectively improved recovery of synaptic potentials and intrinsic optical signals in these vulnerable conditions. Fluorescence imaging and genetic deletion of a presynaptic Zn transporter confirmed synaptic release as the primary contributor to extracellular accumulation and deleterious consequences of Zn during SD. These results demonstrate a role for synaptic Zn release in deleterious consequences of SD and show that targeted extracellular chelation could be useful for disorders where repetitive SD enlarges infarcts in injured tissues.
ISSN:1095-953X