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Updated: Jul 1, 2026

A Cell Culture Model for Studying the Role of Neuron-Glia Interactions in Ischemia
Published on: November 14, 2020
Blockade of microglial glutamate release protects against ischemic brain injury
Hideyuki Takeuchi1, Shijie Jin, Hiromi Suzuki
1Department of Neuroimmunology, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan. htake@riem.nagoya-u.ac.jp
Abstract:
Glutamate released by activated microglia induces excito-neurotoxicity and may contribute to neurodegeneration in numerous neurological diseases including ischemia, inflammation, epilepsy, and neurodegenerative diseases. We observed that the gap junction blocker carbenoxolone (CBX) or the glutaminase inhibitor 6-diazo-5-oxo-L-norleucine (DON) decreased glutamate release from activated microglia and rescued neuronal death in a dose-dependent manner in vitro. In gerbils, treatment with CBX or DON also prevented the delayed death of hippocampal neurons following transient global ischemia. Thus, blockade of microglial glutamate release may be an effective therapeutic strategy against neurodegeneration after ischemic injury.
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