Abstract
Myelination of axons is important for central nervous system function, but oligodendrocytes, which constitute CNS myelin, are vulnerable to excitotoxic injury and death. Although mature oligodendrocytes express functional α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic (AMPA) and kainate-type glutamate receptors, the relative roles of these subtypes in excitotoxicity are not well understood. Using recently developed selective antagonists for subtypes of ionotropic non-NMDA receptors, we addressed this issue. By examining the pharmacological, biochemical, and morphologic features of kainite-induced excitotoxic death, we also determined whether it occurs by apoptosis, necrosis, or both. We conclude that when mature oligodendrocytes die after exposure to kainate: (1) AMPA receptors are the most important mediators, (2) kainate receptors play a smaller role, and (3) death occurs predominantly by necrosis, not apoptosis.
Original language | English (US) |
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Pages (from-to) | 336-348 |
Number of pages | 13 |
Journal | Neurobiology of Disease |
Volume | 14 |
Issue number | 3 |
DOIs | |
State | Published - Dec 2003 |
Externally published | Yes |
Keywords
- AMPA
- Apoptosis
- Demyelination
- Excitotoxicity
- Glutamate
- Kainate
- Murine culture
- Myelin
- Necrosis
- Oligodendrocyte
ASJC Scopus subject areas
- Neurology