| Excitatory Amino Acids and Neuronal Plasticity Softcover Repri Edition Contributor(s): Ben-Ari, Yehezkel (Editor) |
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ISBN: 1468457713 ISBN-13: 9781468457711 Publisher: Springer OUR PRICE: $104.49 Product Type: Paperback - Other Formats Published: July 2013 |
| Additional Information |
| BISAC Categories: - Medical | Pharmacology - Medical | Neuroscience - Science | Life Sciences - Biophysics |
| Dewey: 591.188 |
| Series: Advances in Experimental Medicine and Biology |
| Physical Information: 1.1" H x 7" W x 10" (2.05 lbs) 530 pages |
| Descriptions, Reviews, Etc. |
| Publisher Description: Adult and immature nervous system are capable of considerable "plasticity" and unravelling the underlying mechanisms is one of the principal and most fascinating goals of Neurobiology. A major contribution to our understanding of neural plasticity has come from recent studies in excitato- ry amino acids - which are thought to mediate a large part of the excitatory synaptic transmission on the brain. Important steps in this explosive field are: 1) the synthesis of relatively specific antagonists of the N-methyl-D aspartate (NMDA) and non-NMDA receptors subtypes, 2) the characterization of the unique features of the NMDA receptor channel complex notably its voltage dependent Mg++ blockade, its permeability to calcium and its allosteric modulation by glycine, 3) the demonstration that by virtue of their Ca++ permeability NMDA receptors are involved in many -but not all -synapses in the initiation but not the maintennce of long term potentiation (L TP) an experimented model of learning and memory processes. More recent studies also indicate tha excitatory amino acids also play an important role in developmental plasticity in vivo; in cell cultures low levels of excitatory amino acids have trophic roles and can inhibit or promote neurite growth. Excitatory amino acids also play an important role also in other forms of neural plasticity such as the use dependent permanent changes in neural circuit produced by brief seizures (epileptogenesis) as well as the reactive sprouting and neosynapse formation which take place in epilepsy models and after deafferentiation or lesions. |
