Results 291 to 300 of about 155,151 (336)
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Neuroscience, 1999
Interest in the fundamental mechanisms underlying headache, particularly the pathophysiology of migraine and cluster headache, has lead to the study of the physiology and pharmacology of the trigeminovascular system and its central ramifications. Cats were anaesthetized (60 mg/kg alpha-chloralose, i.p., along with halothane for all surgical procedures)
R J, Storer, P J, Goadsby
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Interest in the fundamental mechanisms underlying headache, particularly the pathophysiology of migraine and cluster headache, has lead to the study of the physiology and pharmacology of the trigeminovascular system and its central ramifications. Cats were anaesthetized (60 mg/kg alpha-chloralose, i.p., along with halothane for all surgical procedures)
R J, Storer, P J, Goadsby
openaire +2 more sources
The role of N-methyl-D-aspartate receptor in Alzheimer's disease
Journal of the Neurological Sciences, 2014Alzheimer's disease (AD) is a neurodegenerative disease characterized by cognitive disorder and memory dysfunction. This kind of cognitive impairment is closely related to synaptic plasticity, in which N-methyl-D-aspartate receptor (NMDAR), which is one of the glutamate receptors, plays a critical role.
Junsi, Zhang +3 more
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Deramciclane inhibits N-methyl-D-aspartate receptor function
Brain Research Bulletin, 2000Effects of the novel anxiolytic drug deramciclane on excitatory amino acid release and transmembrane Ca(2+) ion flux processes were compared in rat cerebrocortical homogenates containing resealed plasmalemma fragments and nerve endings. Deramciclane (10 microM) significantly inhibited [(3)H]D-aspartate release and transmembrane Ca(2+) flux to N-methyl ...
I, Kovács +3 more
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Modeling of N-Methyl-D-Aspartate Receptors
2019Several reduced kinetic models for N-methyl-D-aspartate receptors were derived in order to suit different experimental protocols. Their simultaneous application allows for a step-wise estimation of parameters of a conventional model that is otherwise overparameterized with respect to the existing data.
Denis Shchepakin +2 more
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Opiate physical dependence and N-methyl-d-aspartate receptors
European Journal of Pharmacology, 2004The present review focused the involvement of N-methyl-D-aspartate (NMDA) receptors in morphine physical dependence. The increased levels of extracellular glutamate, NMDA receptor zeta subunit (NR1) mRNA, NMDA receptor epsilon 1 subunit (NR2A) protein, phosphorylated Ca(2+)/calmodulin kinase II (p-CaMKII) protein, c-fos mRNA, c-Fos protein, are ...
Yukihiro, Noda, Toshitaka, Nabeshima
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The promise of N-methyl-d-aspartate receptor antagonists in fibromyalgia
Rheumatic Disease Clinics of North America, 2002There is strong evidence that intravenous administration of ketamine following a standardized protocol could be used as a diagnostic test for a central sensitization in the central nervous system in patients with FM. The combination of a weak opioid and an NMDA-receptor antagonist with few side effects is presently a promise for treatment of pain in a ...
Karl G, Henriksson, Jan, Sörensen
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Excitotoxicity and N‐methyl‐D‐Aspartate receptors
Drug Development Research, 1989AbstractA great deal of new information has been generated over the past decade in the excitatory amino acid (EAA) field. Not only have endogenous EAA such as glutamate and aspartate become recognized as the leading neurotransmitter candidates at the majority of excitatory synapses in the mammalian central nervous system, but it is becoming ...
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Proteolysis of the N-Methyl-d-Aspartate Receptor by Calpain in Situ
The Journal of Pharmacology and Experimental Therapeutics, 2002N-Methyl-D-aspartate (NMDA) receptors are calcium-permeable glutamate receptors that play putative roles in learning, memory, and excitotoxicity. NMDA receptor-mediated calcium entry can activate the calcium-dependent protease calpain, leading to substrate degradation. The major NMDA receptor 2 (NR2) subunits of the receptor are in vitro substrates for
Rodney P, Guttmann +5 more
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Molecular Pharmacology, 2002
A large number of structurally diverse compounds act as open-channel blockers of NMDA receptors. They may share discrete or overlapping binding sites within the channel. In this study, the effects of mutations in and around the membrane-spanning and pore-
K. Kashiwagi +6 more
semanticscholar +1 more source
A large number of structurally diverse compounds act as open-channel blockers of NMDA receptors. They may share discrete or overlapping binding sites within the channel. In this study, the effects of mutations in and around the membrane-spanning and pore-
K. Kashiwagi +6 more
semanticscholar +1 more source
Blockade of N-methyl-D-aspartate receptors may protect against ischemic damage in the brain.
Science, 1984R. Simon +3 more
semanticscholar +1 more source