Results 251 to 260 of about 25,057,876 (282)
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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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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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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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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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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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Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology, 2001
Shouji Takahashi +2 more
exaly
Shouji Takahashi +2 more
exaly

