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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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. |
doi_str_mv | 10.1371/journal.pone.0008309 |
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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0008309</identifier><identifier>PMID: 20016851</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>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</subject><ispartof>PloS one, 2009-12, Vol.4 (12), p.e8309-e8309</ispartof><rights>COPYRIGHT 2009 Public Library of Science</rights><rights>2009 Sakatani et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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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.</description><subject>Acoustic startle response</subject><subject>Acoustic Stimulation</subject><subject>Activation</subject><subject>Activity patterns</subject><subject>Advanced glycosylation end products</subject><subject>Alzheimer's disease</subject><subject>Animals</subject><subject>Anxiety</subject><subject>Arthritis</subject><subject>Auditory stimuli</subject><subject>Biochemistry</subject><subject>Biology</subject><subject>Brain research</subject><subject>Cell surface</subject><subject>Clonal deletion</subject><subject>Cues</subject><subject>Diabetes</subject><subject>Diabetes and Endocrinology</subject><subject>Diabetes mellitus</subject><subject>Emotional disorders</subject><subject>Experiments</subject><subject>Fear conditioning</subject><subject>Gene Deletion</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Glycosylation</subject><subject>Hyperactivity</subject><subject>Hyperkinesis - genetics</subject><subject>Hyperkinesis - physiopathology</subject><subject>Hypoxia</subject><subject>Immunoglobulins</subject><subject>Ligands</subject><subject>Light</subject><subject>Medical research</subject><subject>Memory tasks</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Neurodegenerative diseases</subject><subject>Neurological Disorders/Alzheimer Disease</subject><subject>Neurological Disorders/Cerebrovascular Disease</subject><subject>Neuroscience/Behavioral Neuroscience</subject><subject>Population</subject><subject>Receptor for Advanced Glycation End Products</subject><subject>Receptors</subject><subject>Receptors, Immunologic - genetics</subject><subject>Receptors, Immunologic - metabolism</subject><subject>Reflex, Startle - physiology</subject><subject>Reproducibility of Results</subject><subject>Rodents</subject><subject>Science</subject><subject>Sensitivity</subject><subject>Sensitivity analysis</subject><subject>Sepsis</subject><subject>Spatial analysis</subject><subject>Spatial memory</subject><subject>Startle response</subject><subject>Traumatic brain injury</subject><subject>University 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of RAGE causes hyperactivity and increased sensitivity to auditory stimuli in mice</title><author>Sakatani, Seiichi ; Yamada, Kazuyuki ; Homma, Chihiro ; Munesue, Seiichi ; Yamamoto, Yasuhiko ; Yamamoto, Hiroshi ; Hirase, Hajime</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c804t-4a8804ce357eba8d7cc1f1fa240fc9a19f0f6b484d21a4782fe36510e119b91f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acoustic startle response</topic><topic>Acoustic Stimulation</topic><topic>Activation</topic><topic>Activity patterns</topic><topic>Advanced glycosylation end products</topic><topic>Alzheimer's disease</topic><topic>Animals</topic><topic>Anxiety</topic><topic>Arthritis</topic><topic>Auditory stimuli</topic><topic>Biochemistry</topic><topic>Biology</topic><topic>Brain research</topic><topic>Cell surface</topic><topic>Clonal deletion</topic><topic>Cues</topic><topic>Diabetes</topic><topic>Diabetes and Endocrinology</topic><topic>Diabetes mellitus</topic><topic>Emotional disorders</topic><topic>Experiments</topic><topic>Fear conditioning</topic><topic>Gene Deletion</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Glycosylation</topic><topic>Hyperactivity</topic><topic>Hyperkinesis - genetics</topic><topic>Hyperkinesis - physiopathology</topic><topic>Hypoxia</topic><topic>Immunoglobulins</topic><topic>Ligands</topic><topic>Light</topic><topic>Medical research</topic><topic>Memory tasks</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Neurodegenerative diseases</topic><topic>Neurological Disorders/Alzheimer Disease</topic><topic>Neurological Disorders/Cerebrovascular Disease</topic><topic>Neuroscience/Behavioral Neuroscience</topic><topic>Population</topic><topic>Receptor for Advanced Glycation End Products</topic><topic>Receptors</topic><topic>Receptors, 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sensitivity to auditory stimuli in mice</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2009-12-15</date><risdate>2009</risdate><volume>4</volume><issue>12</issue><spage>e8309</spage><epage>e8309</epage><pages>e8309-e8309</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.</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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