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EAAT-2 and EAAT-1 in Astrocytes Play the Major Role in Glutamate Uptake in the CNS In 1989, Rosenberg and Aizenman reported that in astrocyte-poor cultures of the rat cerebral cortex, there was a 100-fold increase in neuronal death caused by glutamate neurotoxicity [59]

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These mitochondrial morphological alterationsincluding reduced organelle size, increased membrane density, and cristae disruptionare established ultrastructural hallmarks of ferroptosis and are functionally associated with impaired mitochondrial bioenergetics, including loss of membrane potential, diminished electron transport chain activity, and excessive ROS generation (Figure 2G)