نتایج جستجو برای: nr1 subunit

تعداد نتایج: 88128  

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1999
D V Lissin R C Carroll R A Nicoll R C Malenka M von Zastrow

We have examined the membrane localization of an AMPA receptor subunit (GluR1) and an NMDA receptor subunit (NR1) endogenously expressed in primary cultures of rat hippocampal neurons. In unstimulated cultures, both GluR1 and NR1 subunits were concentrated in SV2-positive synaptic clusters associated with dendritic shafts and spines. Within 5 min after the addition of 100 microM glutamate to th...

Journal: :British journal of anaesthesia 2008
P-H Tan L-C Yang P-T Chiang J S-C Jang H-C Chung C-H Kuo

BACKGROUND N-methyl-D-aspartate (NMDA), alpha-amino-3-hydroxy-5-methylisoxazolone-4-propionic acid (AMPA), and kainate (KA) receptors are members of the ionotropic glutamate receptor (iGluR) family and are increased in inflamed rat skin. These receptors contribute to inflammatory pain. In this study, we have examined whether there is a similar increase in iGluRs in inflamed human skin in the pr...

Journal: :Brain research 2007
Nigel C Noriega Vasilios T Garyfallou Steven G Kohama Henryk F Urbanski

The locus coeruleus (LC) is a major noradrenergic brain nucleus that regulates states of arousal, optimizes task-oriented decision making, and may also play an important role in modulating the activity of the reproductive neuroendocrine axis. Rodent studies have shown that the LC is responsive to glutamate receptor agonists, and that it expresses various glutamate receptor subunits. However, gl...

Journal: :Neuroscience 2010
E Ampuero F J Rubio R Falcon M Sandoval G Diaz-Veliz R E Gonzalez N Earle A Dagnino-Subiabre F Aboitiz F Orrego U Wyneken

It has been postulated that chronic administration of antidepressant drugs induces delayed structural and molecular adaptations at glutamatergic forebrain synapses that might underlie mood improvement. To gain further insight into these changes in the cerebral cortex, rats were treated with fluoxetine (flx) for 4 weeks. These animals showed decreased anxiety and learned helplessness. N-methyl-d...

Journal: :Neuropharmacology 2002
J-H Luo Z-Y Fu G Losi B G Kim K Prybylowski B Vissel S Vicini

We generated expression vectors for N-terminally green fluorescent protein -tagged NR2A and NR2B subunits (GFP-NR2A and GFP-NR2B). Both constructs expressed GFP and formed functional NMDA channels with similar properties to untagged controls when co-transfected with NR1 subunit partner in HEK293 cells. Primary cultured hippocampal neurons were transfected at five days in vitro with these vector...

Journal: :Neuropharmacology 2005
K T LePage J E Ishmael C M Low S F Traynelis T F Murray

The N-methyl-D-aspartate receptor (NMDAR) antagonists: MK-801, phencyclidine and ketamine are open-channel blockers with limited clinical value due to psychotomimetic effects. Similarly, the psychotomimetic effects of the dextrorotatory opioids, dextromethorphan and its metabolite dextrorphan, derive from their NMDAR antagonist actions. Differences in the use dependency of blockade, however, su...

Journal: :The Journal of biological chemistry 1998
S R Arden J D Sinor W K Potthoff E Aizenman

Cyanide can potentiate N-methyl-D-aspartate receptor-mediated physiological responses in neurons. Here we show that this phenomenon may be attributable to a subunit-specific chemical modification of the receptor directly by the toxin. N-Methyl-D-aspartate (30 microM)-induced whole cell responses in mature (22-29 days in vitro) rat cortical neurons were potentiated nearly 2-fold by a 3-5-min tre...

Journal: :The Journal of pharmacology and experimental therapeutics 2015
Ethan M Anderson Turi Reeves Katherine Kapernaros John K Neubert Robert M Caudle

Opioid withdrawal causes a dysphoric state that can lead to complications in pain patients and can propagate use in drug abusers and addicts. Opioid withdrawal changes the activity of neurons in the nucleus accumbens, an area rich in both opioid-binding mu opioid receptors and glutamate-binding NMDA receptors. Because the accumbens is an area important for reward and aversion, plastic changes i...

Journal: :Structure 2007
Zeynep Akyol Ataman Lokesh Gakhar Brenda R Sorensen Johannes W Hell Madeline A Shea

Calmodulin (CaM) regulates tetrameric N-methyl-D-aspartate receptors (NMDARs) by binding tightly to the C0 and C1 regions of its NR1 subunit. A crystal structure (2HQW; 1.96 A) of calcium-saturated CaM bound to NR1C1 (peptide spanning 875-898) showed that NR1 S890, whose phosphorylation regulates membrane localization, was solvent protected, whereas the endoplasmic reticulum retention motif was...

Journal: :Molecular pharmacology 2004
Nansheng Chen Bo Li Timothy H Murphy Lynn A Raymond

N-methyl-d-aspartate-type glutamate receptors (NMDARs) are ligand-gated ion channels activated by coagonists glutamate and glycine. NMDARs play a critical role in synaptic plasticity and excitotoxicity, largely because of their high calcium permeability and slow deactivation and desensitization kinetics. NR1 is an obligate subunit in all NMDAR complexes, where it combines with NR2A, 2B, 2C, and...

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