Abstract
Glutamate acts postsynaptically at a variety of receptors, including ionotropic and metabotropic types (Choi, 1988; Collingridge and Lester, 1989; Lipton, 1993). The ionotropic receptors are separated by their prototypic agonists into α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors, kainate receptors, and N-methyl-D-aspartate (NMDA) receptors. The first two types are glutamate-gated cation channels that are relatively impermeable to calcium, whereas the NMDA receptor is a glutamate-gated cation channel with a high permeability to calcium.
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Lynch, D.R., Gallagher, M.J., Lenz, S.J., Anegawa, N.J., Grant, E.L. (1997). Pharmacology of Recombinant NMDA Receptors. In: Monaghan, D.T., Wenthold, R.J. (eds) The Ionotropic Glutamate Receptors. The Receptors. Humana Press. https://doi.org/10.1007/978-1-4612-3962-8_13
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