منابع مشابه
Excitatory amino acids and Parkinson's disease.
SIR: Recently, Klockgether and Turski proposed that antagonists of excitatory amino acids may be beneficial in the treatment of Parkinson's disease 1. This suggestion , previously put torward by others 2-4, is supported by recent findings of animal experiments as weil as by clinical data. On the basis of these findings, a somewhat different conclusion can be drawn about the role of gluta-mate i...
متن کاملExcitatory Amino Acids: Clinical Results with Antagonists
The psychopharmacology of agonists and antagonists of excitatory amino acids is in its infancy relative to the decades of intensive research associated with drugs acting on monoamine neurotransmitter systems. The prototype drug in this class, phencyclidine, and its derivative, ketamine, block the N-methyl-D-aspartate (NMDA) subclass of glutamate receptors with competing with glutamate and witho...
متن کاملExcitatory amino acids and Alzheimer's disease.
Excitatory amino acids (EAA) such as glutamate and aspartate are major transmitters of the cerebral cortex and hippocampus, and EAA mechanisms appear to play a role in learning and memory. Anatomical and biochemical evidence suggests that there is both pre- and postsynaptic disruption of EAA pathways in Alzheimer's disease. Dysfunction of EAA pathways could play a role in the clinical manifesta...
متن کاملExcitatory Amino Acids Interaction and Neurotoxicity
It is supposed that Glu, and OXY are synthesized and stored in the same structure and parts of the brain. Both Glu and its receptors are located in different neurosecretory nuclei of the hypothalamus which are associated with neuroendocrine function. It have been demonstrated the presence of Glu in nucleus Paraventricularis (PVN), nucleus Ventro-Medianus (VMN), nucleus arcuatus, nucleus Supraop...
متن کاملExcitatory amino acids: physiological and pharmacological probes for neuroscience research.
The 2S,3S,4S-isomer (L-CCG-I) of 2-(carboxycyclopropyl)glycine (CCG) is a potent metabotropic glutamate receptor agonist. L-CCG-I depressed monosynaptic excitation in the newborn rat spinal motoneurone at low concentrations well below those causing postsynaptic depolarization. 2S,3R,4S-CCG (L-CCG-IV) is a potent N-methyl-D-aspartate (NMDA)-type agonist. In cultured rat hippocampal neurones, L-C...
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ژورنال
عنوان ژورنال: Journal of Neurology, Neurosurgery & Psychiatry
سال: 1987
ISSN: 0022-3050
DOI: 10.1136/jnnp.50.8.1087