Modification of Hippocampal Markers of Synaptic Plasticity by Memantine in Animal Models of Acute and Repeated Restraint Stress: Implications for Memory and Behavior
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Date
2015
Journal Title
Journal ISSN
Volume Title
Type
Article
Publisher
Humana Press Inc.
Series Info
NeuroMolecular Medicine
17
17
Scientific Journal Rankings
Abstract
Stress is any condition that impairs the balance of the organism physiologically or psychologically. The response to stress involves several neurohormonal consequences. Glutamate is the primary excitatory neurotransmitter in the central nervous system, and its release is increased by stress that predisposes to excitotoxicity in the brain. Memantine is an uncompetitive N-methyl D-aspartate glutamatergic receptors antagonist and has shown beneficial effect on cognitive function especially in Alzheimer�s disease. The aim of the work was to investigate memantine effect on memory and behavior in animal models of acute and repeated restraint stress with the evaluation of serum markers of stress and the expression of hippocampal markers of synaptic plasticity. Forty-two male rats were divided into seven groups (six rats/group): control, acute restraint stress, acute restraint stress with Memantine, repeated restraint stress, repeated restraint stress with Memantine and Memantine groups (two subgroups as positive control). Spatial working memory and behavior were assessed by performance in Y-maze. We evaluated serum cortisol, tumor necrotic factor, interleukin-6 and hippocampal expression of brain-derived neurotrophic factor, synaptophysin and calcium-/calmodulin-dependent protein kinase II. Our results revealed that Memantine improved spatial working memory in repeated stress, decreased serum level of stress markers and modified the hippocampal synaptic plasticity markers in both patterns of stress exposure; in ARS, Memantine upregulated the expression of synaptophysin and brain-derived neurotrophic factor and downregulated the expression of calcium-/calmodulin-dependent protein kinase II, and in repeated restraint stress, it upregulated the expression of synaptophysin and downregulated calcium-/calmodulin-dependent protein kinase II expression. � 2015, Springer Science+Business Media New York.
Description
Scopus
Keywords
Behavior, Memantine, Memory, Restraint, Synaptic plasticity, amino acid receptor blocking agent, biological marker, brain derived neurotrophic factor, calcium calmodulin dependent protein kinase II, hydrocortisone, interleukin 6, memantine, nerve protein, neuroprotective agent, synaptophysin, Syp protein, rat, tumor necrosis factor alpha, acute disease, adverse effects, animal, animal behavior, anxiety, biosynthesis, blood, catalepsy, chemistry, drug effects, drug therapy, etiology, exercise, gene expression regulation, genetics, grooming, hippocampus, male, maze test, mental stress, nerve cell plasticity, nervous system development, pathophysiology, physiological stress, physiology, preclinical study, rat, spatial memory, Wistar rat, Acute Disease, Animals, Anxiety, Behavior, Animal, Biomarkers, Brain-Derived Neurotrophic Factor, Calcium-Calmodulin-Dependent Protein Kinase Type 2, Drug Evaluation, Preclinical, Excitatory Amino Acid Antagonists, Freezing Reaction, Cataleptic, Gene Expression Regulation, Grooming, Hippocampus, Hydrocortisone, Interleukin-6, Male, Maze Learning, Memantine, Nerve Tissue Proteins, Neurogenesis, Neuronal Plasticity, Neuroprotective Agents, Rats, Rats, Wistar, Restraint, Physical, Spatial Memory, Stress, Physiological, Stress, Psychological, Synaptophysin, Tumor Necrosis Factor-alpha