Retrosplenial Cortex Damage Impairs Unimodal Sensory Preconditioning
The retrosplenial cortex (RSC) is positioned at the interface between cortical sensory regions and the structures that compose the medial temporal lobe memory system. It has recently been suggested that 1 functional role of the RSC involves the formation of associations between cues in the environme...
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Veröffentlicht in: | Behavioral neuroscience 2020-06, Vol.134 (3), p.198-207 |
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description | The retrosplenial cortex (RSC) is positioned at the interface between cortical sensory regions and the structures that compose the medial temporal lobe memory system. It has recently been suggested that 1 functional role of the RSC involves the formation of associations between cues in the environment (stimulus-stimulus [S-S] learning; Bucci & Robinson, 2014). This suggestion is based, in part, on the finding that lesions or temporary inactivation of the RSC impair sensory preconditioning. However, all prior studies examining the role of the RSC in sensory preconditioning have used cues from multiple modalities (both visual and auditory stimuli). The purpose of the present experiment was to determine whether the RSC contributes to unimodal sensory preconditioning. In the present study we found that both electrolytic and neurotoxic lesions of the RSC impaired sensory preconditioning with auditory cues. Together with previous experiments, these findings indicate that the RSC contributes to both multisensory and unimodal sensory integration, which suggests a general role for the RSC in linking sensory cues in the environment. |
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It has recently been suggested that 1 functional role of the RSC involves the formation of associations between cues in the environment (stimulus-stimulus [S-S] learning; Bucci & Robinson, 2014). This suggestion is based, in part, on the finding that lesions or temporary inactivation of the RSC impair sensory preconditioning. However, all prior studies examining the role of the RSC in sensory preconditioning have used cues from multiple modalities (both visual and auditory stimuli). The purpose of the present experiment was to determine whether the RSC contributes to unimodal sensory preconditioning. In the present study we found that both electrolytic and neurotoxic lesions of the RSC impaired sensory preconditioning with auditory cues. Together with previous experiments, these findings indicate that the RSC contributes to both multisensory and unimodal sensory integration, which suggests a general role for the RSC in linking sensory cues in the environment.</description><identifier>ISSN: 0735-7044</identifier><identifier>EISSN: 1939-0084</identifier><identifier>DOI: 10.1037/bne0000365</identifier><identifier>PMID: 32150422</identifier><language>eng</language><publisher>United States: American Psychological Association</publisher><subject>Animal ; Animal memory ; Animals ; Auditory Perception - physiology ; Auditory stimuli ; Brain Lesions (Disorders) ; Cerebral Cortex - physiology ; Conditioning, Psychological - physiology ; Cues ; Electrolytes ; Environment ; Gyrus Cinguli - metabolism ; Gyrus Cinguli - physiology ; Learning ; Learning - physiology ; Male ; Memory ; Memory - physiology ; Neurotoxicity ; Neurotoxins ; Preconditioning ; Rats ; Rats, Long-Evans ; Sensory Integration ; Somatosensory cortex ; Temporal cortex ; Temporal Lobe ; Visual stimuli</subject><ispartof>Behavioral neuroscience, 2020-06, Vol.134 (3), p.198-207</ispartof><rights>2020 American Psychological Association</rights><rights>2020, American Psychological Association</rights><rights>Copyright American Psychological Association Jun 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a471t-c6d03439345e4d365d5b658246e907778af10403559d99bd09a39d87ee7803d23</citedby><orcidid>0000-0002-3890-7279</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32150422$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Schoenbaum, Geoffrey</contributor><contributor>Burwell, Rebecca D</contributor><creatorcontrib>Fournier, Danielle I.</creatorcontrib><creatorcontrib>Monasch, Ryan R.</creatorcontrib><creatorcontrib>Bucci, David J.</creatorcontrib><creatorcontrib>Todd, Travis P.</creatorcontrib><title>Retrosplenial Cortex Damage Impairs Unimodal Sensory Preconditioning</title><title>Behavioral neuroscience</title><addtitle>Behav Neurosci</addtitle><description>The retrosplenial cortex (RSC) is positioned at the interface between cortical sensory regions and the structures that compose the medial temporal lobe memory system. It has recently been suggested that 1 functional role of the RSC involves the formation of associations between cues in the environment (stimulus-stimulus [S-S] learning; Bucci & Robinson, 2014). This suggestion is based, in part, on the finding that lesions or temporary inactivation of the RSC impair sensory preconditioning. However, all prior studies examining the role of the RSC in sensory preconditioning have used cues from multiple modalities (both visual and auditory stimuli). The purpose of the present experiment was to determine whether the RSC contributes to unimodal sensory preconditioning. In the present study we found that both electrolytic and neurotoxic lesions of the RSC impaired sensory preconditioning with auditory cues. Together with previous experiments, these findings indicate that the RSC contributes to both multisensory and unimodal sensory integration, which suggests a general role for the RSC in linking sensory cues in the environment.</description><subject>Animal</subject><subject>Animal memory</subject><subject>Animals</subject><subject>Auditory Perception - physiology</subject><subject>Auditory stimuli</subject><subject>Brain Lesions (Disorders)</subject><subject>Cerebral Cortex - physiology</subject><subject>Conditioning, Psychological - physiology</subject><subject>Cues</subject><subject>Electrolytes</subject><subject>Environment</subject><subject>Gyrus Cinguli - metabolism</subject><subject>Gyrus Cinguli - physiology</subject><subject>Learning</subject><subject>Learning - physiology</subject><subject>Male</subject><subject>Memory</subject><subject>Memory - physiology</subject><subject>Neurotoxicity</subject><subject>Neurotoxins</subject><subject>Preconditioning</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Sensory Integration</subject><subject>Somatosensory cortex</subject><subject>Temporal cortex</subject><subject>Temporal Lobe</subject><subject>Visual stimuli</subject><issn>0735-7044</issn><issn>1939-0084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFPFDEUxxuigRW9-AHMJN4Ig-281-30YkIWFBISjMq56U7friUz7djOGvbbW7IIeKGXd3i__PPr-zP2XvATwUF9Wgbi5cFc7rGZ0KBrzlt8xWZcgawVRzxgb3K-LQxylPvsABohOTbNjJ19pynFPPYUvO2rRUwT3VVndrBrqi6H0fqUq5vgh-jK-geFHNO2-paoi8H5ycfgw_ote72yfaZ3D_OQ3Xw5_7m4qK-uv14uTq9qi0pMdTd3HBA0oCR0RdfJ5Vy2Dc5Jc6VUa1eiGIKU2mm9dFxb0K5VRKrl4Bo4ZJ93ueNmOZDrKEzJ9mZMfrBpa6L15v9N8L_MOv4xqkGEVpSAjw8BKf7eUJ7MbdykUJxNg-VaKKRqX6RAoZSguC7U0Y7qyv1yotWjh-Dmvhfz1EuBPzw3f0T_FVGA4x1gR2vGvO1smnzXU-42KZXf3IcZAWjACN3CX_xqlvc</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Fournier, Danielle I.</creator><creator>Monasch, Ryan R.</creator><creator>Bucci, David J.</creator><creator>Todd, Travis P.</creator><general>American Psychological Association</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7RZ</scope><scope>PSYQQ</scope><scope>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3890-7279</orcidid></search><sort><creationdate>20200601</creationdate><title>Retrosplenial Cortex Damage Impairs Unimodal Sensory Preconditioning</title><author>Fournier, Danielle I. ; Monasch, Ryan R. ; Bucci, David J. ; Todd, Travis P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a471t-c6d03439345e4d365d5b658246e907778af10403559d99bd09a39d87ee7803d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal</topic><topic>Animal memory</topic><topic>Animals</topic><topic>Auditory Perception - physiology</topic><topic>Auditory stimuli</topic><topic>Brain Lesions (Disorders)</topic><topic>Cerebral Cortex - physiology</topic><topic>Conditioning, Psychological - physiology</topic><topic>Cues</topic><topic>Electrolytes</topic><topic>Environment</topic><topic>Gyrus Cinguli - metabolism</topic><topic>Gyrus Cinguli - physiology</topic><topic>Learning</topic><topic>Learning - physiology</topic><topic>Male</topic><topic>Memory</topic><topic>Memory - physiology</topic><topic>Neurotoxicity</topic><topic>Neurotoxins</topic><topic>Preconditioning</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Sensory Integration</topic><topic>Somatosensory cortex</topic><topic>Temporal cortex</topic><topic>Temporal Lobe</topic><topic>Visual stimuli</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fournier, Danielle I.</creatorcontrib><creatorcontrib>Monasch, Ryan R.</creatorcontrib><creatorcontrib>Bucci, David J.</creatorcontrib><creatorcontrib>Todd, Travis P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>APA PsycArticles®</collection><collection>ProQuest One Psychology</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Behavioral neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fournier, Danielle I.</au><au>Monasch, Ryan R.</au><au>Bucci, David J.</au><au>Todd, Travis P.</au><au>Schoenbaum, Geoffrey</au><au>Burwell, Rebecca D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retrosplenial Cortex Damage Impairs Unimodal Sensory Preconditioning</atitle><jtitle>Behavioral neuroscience</jtitle><addtitle>Behav Neurosci</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>134</volume><issue>3</issue><spage>198</spage><epage>207</epage><pages>198-207</pages><issn>0735-7044</issn><eissn>1939-0084</eissn><abstract>The retrosplenial cortex (RSC) is positioned at the interface between cortical sensory regions and the structures that compose the medial temporal lobe memory system. 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subjects | Animal Animal memory Animals Auditory Perception - physiology Auditory stimuli Brain Lesions (Disorders) Cerebral Cortex - physiology Conditioning, Psychological - physiology Cues Electrolytes Environment Gyrus Cinguli - metabolism Gyrus Cinguli - physiology Learning Learning - physiology Male Memory Memory - physiology Neurotoxicity Neurotoxins Preconditioning Rats Rats, Long-Evans Sensory Integration Somatosensory cortex Temporal cortex Temporal Lobe Visual stimuli |
title | Retrosplenial Cortex Damage Impairs Unimodal Sensory Preconditioning |
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