Deletion of RAGE causes hyperactivity and increased sensitivity to auditory stimuli in mice

The receptor for advanced glycation end-products (RAGE) is a multi-ligand receptor that belongs to the immunoglobulin superfamily of cell surface receptors. In diabetes and Alzheimer's disease, pathological progression is accelerated by activation of RAGE. However, how RAGE influences gross beh...

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Veröffentlicht in:PloS one 2009-12, Vol.4 (12), p.e8309-e8309
Hauptverfasser: Sakatani, Seiichi, Yamada, Kazuyuki, Homma, Chihiro, Munesue, Seiichi, Yamamoto, Yasuhiko, Yamamoto, Hiroshi, Hirase, Hajime
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container_title PloS one
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Yamada, Kazuyuki
Homma, Chihiro
Munesue, Seiichi
Yamamoto, Yasuhiko
Yamamoto, Hiroshi
Hirase, Hajime
description The receptor for advanced glycation end-products (RAGE) is a multi-ligand receptor that belongs to the immunoglobulin superfamily of cell surface receptors. In diabetes and Alzheimer's disease, pathological progression is accelerated by activation of RAGE. However, how RAGE influences gross behavioral activity patterns in basal condition has not been addressed to date. In search for a functional role of RAGE in normal mice, a series of standard behavioral tests were performed on adult RAGE knockout (KO) mice. We observed a solid increase of home cage activity in RAGE KO. In addition, auditory startle response assessment resulted in a higher sensitivity to auditory signal and increased prepulse inhibition in KO mice. There were no significant differences between KO and wild types in behavioral tests for spatial memory and anxiety, as tested by Morris water maze, classical fear conditioning, and elevated plus maze. Our results raise a possibility that systemic therapeutic treatments to occlude RAGE activation may have adverse effects on general activity levels or sensitivity to auditory stimuli.
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Our results raise a possibility that systemic therapeutic treatments to occlude RAGE activation may have adverse effects on general activity levels or sensitivity to auditory stimuli.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>20016851</pmid><doi>10.1371/journal.pone.0008309</doi><tpages>e8309</tpages><oa>free_for_read</oa></addata></record>
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subjects Acoustic startle response
Acoustic Stimulation
Activation
Activity patterns
Advanced glycosylation end products
Alzheimer's disease
Animals
Anxiety
Arthritis
Auditory stimuli
Biochemistry
Biology
Brain research
Cell surface
Clonal deletion
Cues
Diabetes
Diabetes and Endocrinology
Diabetes mellitus
Emotional disorders
Experiments
Fear conditioning
Gene Deletion
Gene expression
Gene Expression Regulation
Glycosylation
Hyperactivity
Hyperkinesis - genetics
Hyperkinesis - physiopathology
Hypoxia
Immunoglobulins
Ligands
Light
Medical research
Memory tasks
Mice
Mice, Knockout
Neurodegenerative diseases
Neurological Disorders/Alzheimer Disease
Neurological Disorders/Cerebrovascular Disease
Neuroscience/Behavioral Neuroscience
Population
Receptor for Advanced Glycation End Products
Receptors
Receptors, Immunologic - genetics
Receptors, Immunologic - metabolism
Reflex, Startle - physiology
Reproducibility of Results
Rodents
Science
Sensitivity
Sensitivity analysis
Sepsis
Spatial analysis
Spatial memory
Startle response
Traumatic brain injury
University graduates
title Deletion of RAGE causes hyperactivity and increased sensitivity to auditory stimuli in mice
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