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A-amino-3-hydroxy-5-methyl-4-isoxazole

AMPAR. (a-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid) receptor a non-NMDA-type ionotropic transmembrane receptor for glutamate that mediates fast synaptic transmission in the central nervous system. [Pg.249]

Non-NMDA ionotropic glutamate receptors (the majority sodium channel containing) can be subdivided into a-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) (comprising cloned subunits GluRl ) and kainate (GluR5-7, KAl-2) preferring receptors, with native receptors most likely to comprise either homo- or heteromeric pentamers of these subunits. [Pg.214]

AMPA a-amino-3-hydroxy-5-methyl-4-isoxazole proprionic acid... [Pg.504]

Fletcher, E. J. and Lodge, D. New developments in the molecular pharmacology of a-amino-3-hydroxy-5-methyl-4-isoxazole propionate and kainate receptors. Pharmacol. Ther. 70 65-89,1996. [Pg.289]

In vitro studies on excitotoxicity suggest that while both NMDA and a-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA)/kainate (KA) receptors can mediate excitotoxicity (see Ch. 15), these classes of glutamate receptors do not do so equally. Experiments with cortical or hippocampal cell cultures suggest that much of the neuronal death associated with brief, intense glutamate exposure is mediated by NMDA receptor activation, probably because this can induce lethal amounts of Ca2+ influx more rapidly than can AMPA/KA receptor stimulation. [Pg.563]

Ionotropic glutamate receptors mediate fast excitatory neurotransmission in practically all areas of the central nervous system (CNS). They are also critical for both the induction and expression of synaptic plasticity, and have been implicated in diverse pathological conditions, such as epilepsy, ischemic brain damage, anxiety, and addiction. There are three subtypes of ionotropic glutamate receptors that are named after their high-affinity agonists as a-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA), N-1nethyl-D-aspartate (NMDA), and kainate (KA) receptors (1). [Pg.27]

Lesions of the basal forebrain cholinergic system using a-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) result in impaired attentional, but not mnemonic, function in rats (Muir et al., 1995) and monkeys (Voytko et al., 1994), an effect which has been confirmed using more selective IgG-saporin lesions (Baxter et al., 1995 Everitt 8c Robbins, 1997). [Pg.56]

C7H10N2O4 (R,S)-a-amino-3-hydroxy-5-methyl-4-isoxazole 74341-63-2 25.00 1.2908 2 11526 C7H1203 6-oxoheptanoic acid 3218-07-2 25.00 1.0590 1... [Pg.232]

Sharp JW, Ross CM, Koehnle TJ, Gietzen DW. 2004. Phosphorylation of Ca /calmodulin dependent protein kinase type II and the a-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptor in response to a threonine-devoid diet. Neuroscience 126 1053-1062. [Pg.268]

Pharmacology and Mechanism of Action. Topiramate is a sulfamate-substituted monosaccharide that has multiple modes of action involving voltage-dependent sodium channels, GABA receptors, and antagonism of a-amino-3-hydroxy-5-methyl-4-isoxazole-4-propionic acid (AMPA) subtype glutamate receptors. ... [Pg.1043]


See other pages where A-amino-3-hydroxy-5-methyl-4-isoxazole is mentioned: [Pg.119]    [Pg.67]    [Pg.267]    [Pg.273]    [Pg.351]    [Pg.227]    [Pg.75]    [Pg.23]    [Pg.389]    [Pg.76]    [Pg.140]    [Pg.275]    [Pg.315]    [Pg.314]    [Pg.91]    [Pg.117]    [Pg.174]    [Pg.1796]    [Pg.378]    [Pg.243]    [Pg.260]    [Pg.60]    [Pg.152]    [Pg.152]    [Pg.362]   


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3-Amino-5-methyl-isoxazole

5- Amino-4-hydroxy-4-methyl

5- methyl-3 - isoxazole

A-Amino-3-hydroxy-5-methyl-4-isoxazole propionate

Amino hydroxy

Isoxazoles amino

Isoxazoles hydroxy

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