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Kinetic basis of partial agonism at NMDA receptors
by
Kussius, Cassandra L
, Popescu, Gabriela K
in
Action Potentials - drug effects
/ Agonists (Biochemistry)
/ Alanine - chemistry
/ Alanine - pharmacology
/ Amino Acids, Cyclic - pharmacology
/ Animal Genetics and Genomics
/ Animals
/ Behavioral Sciences
/ Binding Sites
/ Biological Techniques
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Line
/ Cell Membrane - drug effects
/ Cell Membrane - physiology
/ Cycloserine - chemistry
/ Cycloserine - pharmacology
/ Excitatory Amino Acid Agents - chemistry
/ Excitatory Amino Acid Agents - pharmacology
/ Glutamates - chemistry
/ Glutamates - pharmacology
/ Glutamic Acid - chemistry
/ Glutamic Acid - metabolism
/ Glycine - chemistry
/ Glycine - metabolism
/ Humans
/ Kinetics
/ Kynurenic Acid - analogs & derivatives
/ Kynurenic Acid - pharmacology
/ Ligands
/ Methyl aspartate
/ Models, Molecular
/ Neural receptors
/ Neurobiology
/ Neurosciences
/ Physiological aspects
/ Properties
/ Rats
/ Receptors, N-Methyl-D-Aspartate - agonists
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
/ Receptors, N-Methyl-D-Aspartate - metabolism
2009
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Kinetic basis of partial agonism at NMDA receptors
by
Kussius, Cassandra L
, Popescu, Gabriela K
in
Action Potentials - drug effects
/ Agonists (Biochemistry)
/ Alanine - chemistry
/ Alanine - pharmacology
/ Amino Acids, Cyclic - pharmacology
/ Animal Genetics and Genomics
/ Animals
/ Behavioral Sciences
/ Binding Sites
/ Biological Techniques
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Line
/ Cell Membrane - drug effects
/ Cell Membrane - physiology
/ Cycloserine - chemistry
/ Cycloserine - pharmacology
/ Excitatory Amino Acid Agents - chemistry
/ Excitatory Amino Acid Agents - pharmacology
/ Glutamates - chemistry
/ Glutamates - pharmacology
/ Glutamic Acid - chemistry
/ Glutamic Acid - metabolism
/ Glycine - chemistry
/ Glycine - metabolism
/ Humans
/ Kinetics
/ Kynurenic Acid - analogs & derivatives
/ Kynurenic Acid - pharmacology
/ Ligands
/ Methyl aspartate
/ Models, Molecular
/ Neural receptors
/ Neurobiology
/ Neurosciences
/ Physiological aspects
/ Properties
/ Rats
/ Receptors, N-Methyl-D-Aspartate - agonists
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
/ Receptors, N-Methyl-D-Aspartate - metabolism
2009
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Kinetic basis of partial agonism at NMDA receptors
by
Kussius, Cassandra L
, Popescu, Gabriela K
in
Action Potentials - drug effects
/ Agonists (Biochemistry)
/ Alanine - chemistry
/ Alanine - pharmacology
/ Amino Acids, Cyclic - pharmacology
/ Animal Genetics and Genomics
/ Animals
/ Behavioral Sciences
/ Binding Sites
/ Biological Techniques
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Line
/ Cell Membrane - drug effects
/ Cell Membrane - physiology
/ Cycloserine - chemistry
/ Cycloserine - pharmacology
/ Excitatory Amino Acid Agents - chemistry
/ Excitatory Amino Acid Agents - pharmacology
/ Glutamates - chemistry
/ Glutamates - pharmacology
/ Glutamic Acid - chemistry
/ Glutamic Acid - metabolism
/ Glycine - chemistry
/ Glycine - metabolism
/ Humans
/ Kinetics
/ Kynurenic Acid - analogs & derivatives
/ Kynurenic Acid - pharmacology
/ Ligands
/ Methyl aspartate
/ Models, Molecular
/ Neural receptors
/ Neurobiology
/ Neurosciences
/ Physiological aspects
/ Properties
/ Rats
/ Receptors, N-Methyl-D-Aspartate - agonists
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
/ Receptors, N-Methyl-D-Aspartate - metabolism
2009
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Journal Article
Kinetic basis of partial agonism at NMDA receptors
2009
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Overview
The authors propose a mechanism of partial agonism, showing that partial agonists of both GluN1 and GluN2 NMDA receptor subunits have similar effects on the NMDA receptor activation reaction and they increase the height of all energy barriers during NMDA receptor activation. This contrasts with the localized effects observed for pentameric ligand-gated channels.
Activation of ligand-gated channels is initiated by the binding of small molecules at extracellular sites and culminates with the opening of a membrane-embedded pore. To investigate how perturbations at ligand-binding domains influence the gating reaction, we examined current traces recorded from individual NMDA receptors in the presence of several subunit-specific partial agonists. We found that low-efficacy agonists acting at either the glycine-binding or the glutamate-binding NMDA receptor subunits had very similar effects on the receptor's activation reaction, possibly reflecting a high degree of coupling between the two subunit types during gating. In addition, we found that partial agonists increased the height of all energy barriers encountered by NMDA receptors during activation. This result stands in sharp contrast to the localized effects that have been observed for pentameric ligand-gated channels and may represent a previously unknown mechanism by which partial agonists reduce receptor activity.
Publisher
Nature Publishing Group US,Nature Publishing Group
Subject
Action Potentials - drug effects
/ Amino Acids, Cyclic - pharmacology
/ Animal Genetics and Genomics
/ Animals
/ Biomedical and Life Sciences
/ Cell Membrane - drug effects
/ Excitatory Amino Acid Agents - chemistry
/ Excitatory Amino Acid Agents - pharmacology
/ Humans
/ Kinetics
/ Kynurenic Acid - analogs & derivatives
/ Kynurenic Acid - pharmacology
/ Ligands
/ Rats
/ Receptors, N-Methyl-D-Aspartate - agonists
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
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