An N-methyl-d-aspartate-receptor dependent, late-phase long-term depression in middle-aged mice identifies no GluN2-subunit bias

Neuroscience ◽  
2011 ◽  
Vol 185 ◽  
pp. 27-38 ◽  
Author(s):  
T. Ahmed ◽  
V. Sabanov ◽  
R. D'Hooge ◽  
D. Balschun
Physiology ◽  
1994 ◽  
Vol 9 (6) ◽  
pp. 256-260
Author(s):  
D Debanne ◽  
SM Thompson

Two opposing types of plasticity at excitatory synapses in the hippocampus, long-term potentiation and depression, require N-methyl-D-aspartate receptor activation and Ca2+ influx for their induction.The direction of the change in synaptic strength is determined by a balance between phosphorylation and dephosphorylation, as regulated by protein kinases and phosphatases that are activated selectively by different levels of intracellular Ca2+.


2015 ◽  
Vol 36 (2) ◽  
pp. 730-739 ◽  
Author(s):  
Tariq Ahmed ◽  
David Blum ◽  
Sylvie Burnouf ◽  
Dominique Demeyer ◽  
Valérie Buée-Scherrer ◽  
...  

Neuron ◽  
1999 ◽  
Vol 23 (3) ◽  
pp. 559-568 ◽  
Author(s):  
Sohyun Ahn ◽  
David D. Ginty ◽  
David J. Linden

2021 ◽  
pp. 113630
Author(s):  
Izabelle Dias Benfato ◽  
Ana Carolina Silvares Quintanilha ◽  
Jessica Salles Henrique ◽  
Melyssa Alves Souza ◽  
Barbara dos Anjos Rosário ◽  
...  

2019 ◽  
Author(s):  
Rand S. Eid ◽  
Stephanie E. Lieblich ◽  
Sarah J. Wong ◽  
Liisa A.M. Galea

AbstractOvarian hormones influence the outcomes of stress exposure and are implicated in stress-related disorders including depression, yet their roles are often complex and seemingly contradictory. Importantly, depression and stress exposure are associated with immune dysregulation, and ovarian hormones have immunomodulatory properties. However, how ovarian hormones can influence the inflammatory outcomes of stress exposure is poorly understood. Here, we examined the effects of long-term ovariectomy on the behavioral and neuroinflammatory outcomes of sub-chronic stress exposure in middle-aged mice. Briefly, sham-operated and ovariectomized mice were assigned to non-stress groups or exposed to 6 days of variable stress. Mice were assessed on a battery of behavioral tests, and cytokine concentrations were quantified in the frontal cortex and hippocampus. In the frontal cortex, postsynaptic density protein-95 expression was examined as an index of excitatory synapse number and/or stability, and phosphorylated mitogen-activated protein kinases (MAPKs) were measured to explore potential cell signaling pathways elicited by stress exposure and/or ovarian hormones. Long-term ovariectomy modified the central cytokine profile by robustly reducing cytokine concentrations in the frontal cortex and modestly increasing concentrations in the hippocampus. Under non-stress conditions, long-term ovariectomy also reduced extracellular signal-regulated kinase (ERK) phosphoprotein expression in the frontal cortex and increased some measures of depressive-like behavior. The effects of sub-chronic stress exposure were however more pronounced in sham-operated mice. Notably, in sham-operated mice only, sub-chronic stress exposure increased IL-1β and IL-6:IL-10 ratio in the frontal cortex and hippocampus and reduced pERK1/2 expression in the frontal cortex. Further, although sub-chronic stress exposure increased anhedonia-like behavior regardless of ovarian status, it increased passive-coping behavior in sham-operated mice only. These data indicate that long-term ovariectomy has potent effects on the central cytokine milieu and dictates the neuroinflammatory and behavioral effects of sub-chronic stress exposure in middle-aged mice. These findings therefore suggest that the immunomodulatory properties of ovarian hormones are of relevance in the context of stress and possibly depression.


2019 ◽  
Vol 3 ◽  
pp. 239821281984821 ◽  
Author(s):  
TVP Bliss ◽  
GL Collingridge

In this article, we describe our involvement in the early days of research into long-term potentiation. We start with a description of the early experiments conducted in Oslo and London where long-term potentiation was first characterised. We discuss the ways in which the molecular pharmacology of glutamate receptors control the induction and expression of long-term potentiation and its counterpart, long-term depression. We then go on to summarise the extraordinary advances in understanding the cellular mechanisms of synaptic plasticity that have taken place in the subsequent half century. Finally, the increasing evidence that impaired long-term potentiation is a core feature of many brain disorders (LToPathies) is addressed by way of a few selected examples.


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