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Role of neuronal NR2B subunit-containing NMDA receptor-mediated Ca2+ influx and astrocytic activation in cultured mouse cortical neurons and astrocytes

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1098-1136(199712)21:4<390::aid-glia6>3.0.co;2-7openalex-snapshot
Opposite influence of the metabotropic glutamate receptor subtypes mGlu3 and -5 on astrocyte proliferation in culture
inferredcites →https://doi.org/10.1002/(sici)1098-1136(199903)26:1<1::aid-glia1>3.0.co;2-zopenalex-snapshot
Mature hippocampal astrocytes exhibit functional metabotropic and ionotropic glutamate receptors in situ
inferredcites →https://doi.org/10.1002/(sici)1098-1136(20000101)29:1<70::aid-glia7>3.0.co;2-vopenalex-snapshot
Metabotropic glutamate receptors in acutely isolated hippocampal astrocytes: Developmental changes of mGluR5 mRNA and functional expression
inferredcites →https://doi.org/10.1002/ana.410240411openalex-snapshot
The glutamate antagonist MK‐801 reduces focal ischemic brain damage in the rat
inferredcites →https://doi.org/10.1016/0014-2999(89)90275-6openalex-snapshot
Ifenprodil and SL 82.0715 are antagonists at the polyamine site of the N-methyl-D-aspartate (NMDA) receptor
inferredcites →https://doi.org/10.1016/0024-3205(94)00392-0openalex-snapshot
Excitatory amino acid receptor antagonists: A novel treatment for ischemic cerebrovascular diseases
inferredcites →https://doi.org/10.1016/0896-6273(93)90317-kopenalex-snapshot
Developmental switch in the expression of NMDA receptors occurs in vivo and in vitro
inferredcites →https://doi.org/10.1016/0896-6273(94)90445-6openalex-snapshot
Mutational analysis of the glycine-binding site of the NMDA receptor: Structural similarity with bacterial amino acid-binding proteins
inferredcites →https://doi.org/10.1016/j.conb.2005.05.004openalex-snapshot
Glutamate receptor ion channels
inferredcites →https://doi.org/10.1016/s0022-3565(24)37138-1openalex-snapshot
Ro 25–6981, a Highly Potent and Selective Blocker of N-Methyl-d-aspartate Receptors Containing the NR2B Subunit. Characterization in Vitro
inferredcites →https://doi.org/10.1016/s0022-3565(25)13281-3openalex-snapshot
Ifenprodil and SL 82.0715 as cerebral anti-ischemic agents. I. Evidence for efficacy in models of focal cerebral ischemia.
inferredcites →https://doi.org/10.1016/s0022-3565(25)13282-5openalex-snapshot
Ifenprodil and SL 82.0715 as cerebral anti-ischemic agents. II. Evidence for N-methyl-D-aspartate receptor antagonist properties.
inferredcites →https://doi.org/10.1016/s0024-3205(99)00036-3openalex-snapshot
Effects of the non-competitive NMDA receptor antagonist ifenprodil on the morphine-induced place preference in mice
inferredcites →https://doi.org/10.1016/s0026-895x(25)13275-6openalex-snapshot
Ifenprodil discriminates subtypes of the N-methyl-D-aspartate receptor: selectivity and mechanisms at recombinant heteromeric receptors.
inferredcites →https://doi.org/10.1016/s0031-6997(24)01394-2openalex-snapshot
The Glutamate Receptor Ion Channels
inferredcites →https://doi.org/10.1016/s0031-6997(25)00025-0openalex-snapshot
Excitatory amino acid receptors in the vertebrate central nervous system.
inferredcites →https://doi.org/10.1016/s0165-6147(96)80008-3openalex-snapshot
NMDA receptors: from genes to channels
inferredcites →https://doi.org/10.1016/s0166-2236(97)01139-9openalex-snapshot
Reactive astrocytes: cellular and molecular cues to biological function
inferredcites →https://doi.org/10.1016/s0301-0082(99)00007-6openalex-snapshot
Subunit- and site-specific pharmacology of the NMDA receptor channel
inferredcites →https://doi.org/10.1016/s0896-6273(00)80481-xopenalex-snapshot
Metabotropic Glutamate Receptor–Mediated Control of Neurotransmitter Release
inferredcites →https://doi.org/10.1016/s0959-4388(00)00215-4openalex-snapshot
NMDA receptor subunits: diversity, development and disease
inferredcites →https://doi.org/10.1038/358036a0openalex-snapshot
Molecular diversity of the NMDA receptor channel
inferredcites →https://doi.org/10.1038/373612a0openalex-snapshot
Synchronized oscillations in interneuron networks driven by metabotropic glutamate receptor activation
inferredcites →https://doi.org/10.1038/jcbfm.1990.120openalex-snapshot
Focal Cerebral Ischemia in the Cat: Pretreatment with a Competitive NMDA Receptor Antagonist, D-CPP-ene
inferredcites →https://doi.org/10.1038/jcbfm.1993.77openalex-snapshot
Characterization of the Cerebroprotective Efficacy of the Competitive NMDA Receptor Antagonist CGP40116 in a Rat Model of Focal Cerebral Ischemia: An in vivo Magnetic Resonance Imaging Study
inferredcites →https://doi.org/10.1038/jcbfm.1995.24openalex-snapshot
In vivo Models of Cerebral Ischemia: Effects of Parenterally Administered NMDA Receptor Glycine Site Antagonists
inferredcites →https://doi.org/10.1038/jcbfm.1995.25openalex-snapshot
The Neuroprotective Effect of the Glycine Site Antagonist 3 R -(+)- cis -4-Methyl-HA966 (L-687,414) in a Rat Model of Focal Ischaemia
inferredcites →https://doi.org/10.1046/j.1471-4159.2001.00369.xopenalex-snapshot
Glutamate receptor subunit expression in primary neuronal and secondary glial cultures
inferredcites →https://doi.org/10.1073/pnas.89.18.8552openalex-snapshot
Alternative splicing generates functionally distinct N-methyl-D-aspartate receptors.
inferredcites →https://doi.org/10.1111/j.0953-816x.2003.03119.xopenalex-snapshot
Neuronal protein kinase Cγ‐dependent proliferation and hypertrophy of spinal cord astrocytes following repeated in vivo administration of morphine
inferredcites →https://doi.org/10.1111/j.1471-4159.2005.03136.xopenalex-snapshot
Implication of cyclin‐dependent kinase 5 in the development of psychological dependence on and behavioral sensitization to morphine
inferredcites →https://doi.org/10.1111/j.1476-5381.1996.tb15243.xopenalex-snapshot
Characterization of metabotropic glutamate receptor‐mediated facilitation of N‐methyl‐D‐aspartate depolarization of neocortical neurones
inferredcites →https://doi.org/10.1126/science.1329206openalex-snapshot
Molecular Diversity of Glutamate Receptors and Implications for Brain Function
inferredcites →https://doi.org/10.1126/science.7716515openalex-snapshot
Calcium Signaling in Neurons: Molecular Mechanisms and Cellular Consequences
inferredcites →https://doi.org/10.1146/annurev.ne.17.030194.000335openalex-snapshot
Cloned Glutamate Receptors
inferredcites →https://doi.org/10.1152/jn.1999.82.6.2956openalex-snapshot
Evidence for Involvement of Group II/III Metabotropic Glutamate Receptors in NMDA Receptor–Independent Long-Term Potentiation in Area CA1 of Rat Hippocampus
inferredcites →https://doi.org/10.1152/physrev.1994.74.3.723openalex-snapshot
N-methyl-D-aspartic acid receptor structure and function
inferredcites →https://doi.org/10.1523/jneurosci.11-12-03685.1991openalex-snapshot
New roles for glia
inferredcites →https://doi.org/10.1523/jneurosci.14-05-03180.1994openalex-snapshot
Regional and developmental heterogeneity in splicing of the rat brain NMDAR1 mRNA
inferredcites →https://doi.org/10.1523/jneurosci.21-19-j0005.2001openalex-snapshot
Postsynaptic Depolarization Scales Quantal Amplitude in Cortical Pyramidal Neurons
inferredcites →https://doi.org/10.2466/pr0.1994.74.3.723openalex-snapshot
Empirical Relationships between Need for Cognition and Cognitive Style: Implications for Consumer Psychology

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4643343openalex-extracted
Features of Astrocytic NMDA Receptors
inferred← citeshttps://doi.org/10.1002/glia.22288openalex-snapshot
Artifact versus reality—How astrocytes contribute to synaptic events
inferred← citeshttps://doi.org/10.1002/syn.21733openalex-snapshot
Astrocytic activation in the anterior cingulate cortex is critical for sleep disorder under neuropathic pain
inferred← citeshttps://doi.org/10.1007/s12031-010-9404-3openalex-snapshot
Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) Stimulates Proliferation of Reactive Astrocytes In Vitro
inferred← citeshttps://doi.org/10.1007/s40005-024-00667-wopenalex-snapshot
Intranasal delivery of siRNA targeting NR2B attenuates cancer-associated neuropathic pain
inferred← citeshttps://doi.org/10.1016/j.advms.2024.03.008openalex-snapshot
Impact of NMDA receptors block versus GABA-A receptors modulation on synaptic plasticity and brain electrical activity in metabolic syndrome
inferred← citeshttps://doi.org/10.1016/j.bbi.2011.04.002openalex-snapshot
Neuronal NR2B-containing NMDA receptor mediates spinal astrocytic c-Jun N-terminal kinase activation in a rat model of neuropathic pain
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2015.04.002openalex-snapshot
NMDA receptor NR2B subunits contribute to PTZ-kindling-induced hippocampal astrocytosis and oxidative stress
inferred← citeshttps://doi.org/10.1016/j.cyto.2020.155366openalex-snapshot
Alteration in the expression of inflammatory cytokines in primary hippocampal astrocytes in response to MK-801 through ERK1/2 and PI3K signals
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118267openalex-snapshot
Aniline analogues as synchronized Ca2+ oscillation modulators: structure-activity relationship and mechanism
inferred← citeshttps://doi.org/10.1080/1028415x.2018.1478653openalex-snapshot
Apigenin reverses behavioural impairments and cognitive decline in kindled mice via CREB-BDNF upregulation in the hippocampus
inferred← citeshttps://doi.org/10.1080/17482960701523124openalex-snapshot
Survey of ALS‐associated factors potentially promoting Ca2+overload of motor neurons
inferred← citeshttps://doi.org/10.1093/pm/pnw358openalex-snapshot
B Vitamins Potentiate Acute Morphine Antinociception and Attenuate the Development of Tolerance to Chronic Morphine in Mice
inferred← citeshttps://doi.org/10.1111/j.1471-4159.2009.06087.xopenalex-snapshot
Inhibiting astrocytic activation: a novel analgesic mechanism of ketamine at the spinal level?
inferred← citeshttps://doi.org/10.1111/j.1471-4159.2011.07465.xopenalex-snapshot
Ifenprodil restores GDNF‐evoked Ca2+ signalling and Na+/K+‐ATPase expression in inflammation‐pretreated astrocytes
inferred← citeshttps://doi.org/10.1134/s0006297924060063openalex-snapshot
Astrocytic NMDA Receptors
inferred← citeshttps://doi.org/10.1155/ane/2861013openalex-snapshot
N‐Methyl‐D‐Aspartate Receptor (NMDAR) Antibodies Induce Diverse Calcium Activity Patterns on Cultured Astrocytes and Astrocyte–Neuron Cocultures
inferred← citeshttps://doi.org/10.11606/t.42.2011.tde-10022012-132908openalex-snapshot
Envolvimento de Rac1 na excitotoxicidade induzida por NMDA na retina de ratos.
inferred← citeshttps://doi.org/10.11620/ijob.2020.45.3.84openalex-snapshot
Participation of D-serine and NR2 subunits in EphA4-mediated trigeminal neuropathic pain
inferred← citeshttps://doi.org/10.1177/17448069241239231openalex-snapshot
Esketamine inhibits the c-Jun N-terminal kinase pathway in the spinal dorsal horn to relieve bone cancer pain in rats
inferred← citeshttps://doi.org/10.1179/1743132812y.0000000113openalex-snapshot
Preventive effects of AdR-siPTEN through the regulation of NMDA receptor NR2B subunit in trigeminal ganglia of migraine rats
inferred← citeshttps://doi.org/10.1186/1742-2094-8-6openalex-snapshot
Inhibition of spinal astrocytic c-Jun N-terminal kinase (JNK) activation correlates with the analgesic effects of ketamine in neuropathic pain
inferred← citeshttps://doi.org/10.1371/journal.pone.0126314openalex-snapshot
A Metabotropic-Like Flux-Independent NMDA Receptor Regulates Ca2+ Exit from Endoplasmic Reticulum and Mitochondrial Membrane Potential in Cultured Astrocytes
inferred← citeshttps://doi.org/10.1371/journal.pone.0145651openalex-snapshot
Reactive Transformation and Increased BDNF Signaling by Hippocampal Astrocytes in Response to MK-801
inferred← citeshttps://doi.org/10.1523/jneurosci.1727-06.2006openalex-snapshot
Odorant Deprivation Reversibly Modulates Transsynaptic Changes in the NR2B-Mediated CREB Pathway in Mouse Piriform Cortex
inferred← citeshttps://doi.org/10.2174/1570159x11311030002openalex-snapshot
NMDA Receptors in Glial Cells: Pending Questions
inferred← citeshttps://doi.org/10.2174/9798898815646126010004openalex-snapshot
Unveiling the Role of Glutamate and NMDA Receptors in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.24275/uami.00000028popenalex-snapshot
Papel de las especies reactivas de oxígeno producidas por NADPH-Oxidasa en el proceso neuroinflamatorio inducido por daño excitotóxico
inferred← citeshttps://doi.org/10.31857/s0320972524060069openalex-snapshot
Features of Astrocytic NMDA Receptors (Review)
inferred← citeshttps://doi.org/10.3389/fnbeh.2019.00163openalex-snapshot
Risperidone Reverses the Downregulation of BDNF in Hippocampal Neurons and MK801-Induced Cognitive Impairment in Rats
inferred← citeshttps://doi.org/10.3389/fncel.2019.00495openalex-snapshot
NMDAR and JNK Activation in the Spinal Trigeminal Nucleus Caudalis Contributes to Masseter Hyperalgesia Induced by Stress
inferred← citeshttps://doi.org/10.3389/fncel.2021.672136openalex-snapshot
Reversible Changes in BDNF Expression in MK-801-Induced Hippocampal Astrocytes Through NMDAR/PI3K/ERK Signaling
inferred← citeshttps://doi.org/10.3389/fnins.2019.00043openalex-snapshot
The Role of NMDA Receptors in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fphar.2020.00092openalex-snapshot
Zerumbone Modulates α2A-Adrenergic, TRPV1, and NMDA NR2B Receptors Plasticity in CCI-Induced Neuropathic Pain In Vivo and LPS-Induced SH-SY5Y Neuroblastoma In Vitro Models
inferred← citeshttps://doi.org/10.5772/intechopen.72975openalex-snapshot
NMDA Receptors in Astroglia: Chronology, Controversies, and Contradictions from a Complex Molecule
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