scholarly journals The &[Alpha]2δ‐1–NMDA Receptor Coupling is Essential for Corticostriatal Long‐Term Potentiation and is Involved in Learning and Memory

2019 ◽  
Vol 33 (S1) ◽  
Author(s):  
JINGJING ZHOU ◽  
De‐Pei Li ◽  
Shao‐Rui Chen ◽  
Yi Luo ◽  
Hui‐Lin Pan
Keyword(s):  
Nmda Receptor ◽  
Learning And Memory ◽  
Long Term Potentiation ◽  
Receptor Coupling ◽  
Term Potentiation

scholarly journals The α2δ-1–NMDA receptor coupling is essential for corticostriatal long-term potentiation and is involved in learning and memory

2018 ◽  
Vol 293 (50) ◽  
pp. 19354-19364 ◽  
Author(s):  
Jing-Jing Zhou ◽  
De-Pei Li ◽  
Shao-Rui Chen ◽  
Yi Luo ◽  
Hui-Lin Pan
Keyword(s):  
Nmda Receptor ◽  
Learning And Memory ◽  
Long Term Potentiation ◽  
Receptor Coupling ◽  
Term Potentiation

Arousing the LTP and learning debate

1997 ◽  
Vol 20 (4) ◽  
pp. 622-623 ◽  
Author(s):  
Stephen Maren
Keyword(s):  
Learning And Memory ◽  
Long Term Potentiation ◽  
Term Potentiation ◽  
Arousal Mechanism

Shors & Matzel provide compelling arguments against a role for hippocampal long-term potentiation (LTP) in mammalian learning and memory. As an alternative, they suggest that LTP is an arousal mechanism. I will argue that this view is not a satisfactory alternative to current conceptions of LTP function.

scholarly journals Defective place cell activity in nociceptin receptor knockout mice with elevated NMDA receptor-dependent long-term potentiation

2005 ◽  
Vol 565 (2) ◽  
pp. 579-591 ◽  
Author(s):  
Franco A. Taverna ◽  
John Georgiou ◽  
Robert J. McDonald ◽  
Nancy S. Hong ◽  
Alexander Kraev ◽  
...  
Keyword(s):  
Nmda Receptor ◽  
Knockout Mice ◽  
Cell Activity ◽  
Long Term Potentiation ◽  
Place Cell ◽  
Term Potentiation ◽  
Nociceptin Receptor

Endogenous secreted amyloid precursor protein-α regulates hippocampal NMDA receptor function, long-term potentiation and spatial memory

2008 ◽  
Vol 31 (2) ◽  
pp. 250-260 ◽  
Author(s):  
Chanel J. Taylor ◽  
David R. Ireland ◽  
Irene Ballagh ◽  
Katie Bourne ◽  
Nicola M. Marechal ◽  
...  
Keyword(s):  
Nmda Receptor ◽  
Spatial Memory ◽  
Amyloid Precursor Protein ◽  
Long Term Potentiation ◽  
Precursor Protein ◽  
Receptor Function ◽  
Term Potentiation ◽  
Nmda Receptor Function

Insights into associative long-term potentiation from computational models of NMDA receptor-mediated calcium influx and intracellular calcium concentration changes

1990 ◽  
Vol 63 (5) ◽  
pp. 1148-1168 ◽  
Author(s):  
W. R. Holmes ◽  
W. B. Levy
Keyword(s):  
Experimental Data ◽  
Nmda Receptor ◽  
Nmda Receptors ◽  
Dendritic Spine ◽  
Long Term Potentiation ◽  
Input Frequency ◽  
Spine Head ◽  
Term Potentiation ◽  
Concentration Changes

1. Because induction of associative long-term potentiation (LTP) in the dentate gyrus is thought to depend on Ca2+ influx through channels controlled by N-methyl-D-aspartate (NMDA) receptors, quantitative modeling was performed of synaptically mediated Ca2+ influx as a function of synaptic coactivation. The goal was to determine whether Ca2+ influx through NMDA-receptor channels was, by itself, sufficient to explain associative LTP, including control experiments and the temporal requirements of LTP. 2. Ca2+ influx through NMDA-receptor channels was modeled at a synapse on a dendritic spine of a reconstructed hippocampal dentate granule cell when 1-115 synapses on spines at different dendritic locations were activated eight times at frequencies of 10-800 Hz. The resulting change in [Ca2+] in the spine head was estimated from the Ca2+ influx with the use of a model of a dendritic spine that included Ca2+ buffers, pumps, and diffusion. 3. To use a compelling model of synaptic activation, we developed quantitative descriptions of the NMDA and non-NMDA receptor-mediated conductances consistent with available experimental data. The experimental data reported for NMDA and non-NMDA receptor-channel properties and data from other non-LTP experiments that separated the NMDA and non-NMDA receptor-mediated components of synaptic events proved to be limiting for particular synaptic variables. Relative to the non-NMDA glutamate-type receptors, 1) the unbinding of transmitter from NMDA receptors had to be slow, 2) the transition from the bound NMDA receptor-transmitter complex to the open channel state had to be even slower, and 3) the average number of NMDA-receptor channels at a single activated synapse on a single spine head that were open and conducting at a given moment in time had to be very small (usually less than 1). 4. With the use of these quantitative synaptic conductance descriptions. Ca2+ influx through NMDA-receptor channels at a synapse was computed for a variety of conditions. For a constant number of pulses, Ca2+ influx was calculated as a function of input frequency and the number of coactivated synapses. When few synapses were coactivated, Ca2+ influx was small, even for high-frequency activation. However, with larger numbers of coactivated synapses, there was a steep increase in Ca2+ influx with increasing input frequency because of the voltage-dependent nature of the NMDA receptor-mediated conductance. Nevertheless, total Ca2+ influx was never increased more than fourfold by increasing input frequency or the number of coactivated synapses.(ABSTRACT TRUNCATED AT 400 WORDS)

scholarly journals Intracellular Domains of NMDA Receptor Subtypes Are Determinants for Long-Term Potentiation Induction

2003 ◽  
Vol 23 (34) ◽  
pp. 10791-10799 ◽  
Author(s):  
Georg Köhr ◽  
Vidar Jensen ◽  
Helmut J. Koester ◽  
Andre L. A. Mihaljevic ◽  
Jo K. Utvik ◽  
...  
Keyword(s):  
Nmda Receptor ◽  
Long Term Potentiation ◽  
Receptor Subtypes ◽  
Term Potentiation ◽  
Intracellular Domains
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