Microglia play beneficial roles in multiple experimental seizure models

Author:

Gibbs‐Shelton Synphane12,Benderoth Jordan13,Gaykema Ronald P.2,Straub Justyna2,Okojie Kenneth A.13,Uweru Joseph O.134,Lentferink Dennis H.13,Rajbanshi Binita2,Cowan Maureen N.134,Patel Brij14,Campos‐Salazar Anthony Brayan14,Perez‐Reyes Edward2,Eyo Ukpong B.134ORCID

Affiliation:

1. Brain Immunology and Glia Center University of Virginia Charlottesville Virginia USA

2. Department of Pharmacology University of Virginia Charlottesville Virginia USA

3. Department of Neuroscience University of Virginia Charlottesville Virginia USA

4. Neuroscience Graduate Program University of Virginia Charlottesville Virginia USA

Abstract

AbstractSeizure disorders are common, affecting both the young and the old. Currently available antiseizure drugs are ineffective in a third of patients and have been developed with a focus on known neurocentric mechanisms, raising the need for investigations into alternative and complementary mechanisms that contribute to seizure generation or its containment. Neuroinflammation, broadly defined as the activation of immune cells and molecules in the central nervous system (CNS), has been proposed to facilitate seizure generation, although the specific cells involved in these processes remain inadequately understood. The role of microglia, the primary inflammation‐competent cells of the brain, is debated since previous studies were conducted using approaches that were less specific to microglia or had inherent confounds. Using a selective approach to target microglia without such side effects, we show a broadly beneficial role for microglia in limiting chemoconvulsive, electrical, and hyperthermic seizures and argue for a further understanding of microglial contributions to contain seizures.

Funder

National Institutes of Health

Owens Family Foundation

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Neurology

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