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Dissociable effects of advanced age on prefrontal cortical and medial temporal lobe ensemble activity
The link between age-related cellular changes within brain regions and larger scale neuronal ensemble dynamics critical for cognition has not been fully elucidated. The present study measured neuron activity within medial prefrontal cortex (PFC), perirhinal cortex (PER), and hippocampal subregion CA...
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Published in: | Neurobiology of aging 2018-10, Vol.70, p.217-232 |
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creator | Hernandez, Abbi R. Reasor, Jordan E. Truckenbrod, Leah M. Campos, Keila T. Federico, Quinten P. Fertal, Kaeli E. Lubke, Katelyn N. Johnson, Sarah A. Clark, Benjamin J. Maurer, Andrew. P. Burke, Sara N. |
description | The link between age-related cellular changes within brain regions and larger scale neuronal ensemble dynamics critical for cognition has not been fully elucidated. The present study measured neuron activity within medial prefrontal cortex (PFC), perirhinal cortex (PER), and hippocampal subregion CA1 of young and aged rats by labeling expression of the immediate-early gene Arc. The proportion of cells expressing Arc was quantified at baseline and after a behavior that requires these regions. In addition, PER and CA1 projection neurons to PFC were identified with retrograde labeling. Within CA1, no age-related differences in neuronal activity were observed in the entire neuron population or within CA1 pyramidal cells that project to PFC. Although behavior was comparable across age groups, behaviorally driven Arc expression was higher in the deep layers of both PER and PFC and lower in the superficial layers of these regions. Moreover, age-related changes in activity levels were most evident within PER cells that project to PFC. These data suggest that the PER-PFC circuit is particularly vulnerable in advanced age. |
doi_str_mv | 10.1016/j.neurobiolaging.2018.06.028 |
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Within CA1, no age-related differences in neuronal activity were observed in the entire neuron population or within CA1 pyramidal cells that project to PFC. Although behavior was comparable across age groups, behaviorally driven Arc expression was higher in the deep layers of both PER and PFC and lower in the superficial layers of these regions. Moreover, age-related changes in activity levels were most evident within PER cells that project to PFC. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495t-2f3273d914a4b0921ee4ecf0588cc53d6508147041bf44d601140f82155f1de63</citedby><cites>FETCH-LOGICAL-c495t-2f3273d914a4b0921ee4ecf0588cc53d6508147041bf44d601140f82155f1de63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,786,790,891,27957,27958</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30031931$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hernandez, Abbi R.</creatorcontrib><creatorcontrib>Reasor, Jordan E.</creatorcontrib><creatorcontrib>Truckenbrod, Leah M.</creatorcontrib><creatorcontrib>Campos, Keila T.</creatorcontrib><creatorcontrib>Federico, Quinten P.</creatorcontrib><creatorcontrib>Fertal, Kaeli E.</creatorcontrib><creatorcontrib>Lubke, Katelyn N.</creatorcontrib><creatorcontrib>Johnson, Sarah A.</creatorcontrib><creatorcontrib>Clark, Benjamin J.</creatorcontrib><creatorcontrib>Maurer, Andrew. P.</creatorcontrib><creatorcontrib>Burke, Sara N.</creatorcontrib><title>Dissociable effects of advanced age on prefrontal cortical and medial temporal lobe ensemble activity</title><title>Neurobiology of aging</title><addtitle>Neurobiol Aging</addtitle><description>The link between age-related cellular changes within brain regions and larger scale neuronal ensemble dynamics critical for cognition has not been fully elucidated. The present study measured neuron activity within medial prefrontal cortex (PFC), perirhinal cortex (PER), and hippocampal subregion CA1 of young and aged rats by labeling expression of the immediate-early gene Arc. The proportion of cells expressing Arc was quantified at baseline and after a behavior that requires these regions. In addition, PER and CA1 projection neurons to PFC were identified with retrograde labeling. Within CA1, no age-related differences in neuronal activity were observed in the entire neuron population or within CA1 pyramidal cells that project to PFC. Although behavior was comparable across age groups, behaviorally driven Arc expression was higher in the deep layers of both PER and PFC and lower in the superficial layers of these regions. Moreover, age-related changes in activity levels were most evident within PER cells that project to PFC. These data suggest that the PER-PFC circuit is particularly vulnerable in advanced age.</description><subject>Aging - physiology</subject><subject>Animals</subject><subject>Arc</subject><subject>Association Learning - physiology</subject><subject>Behavior, Animal</subject><subject>CA1</subject><subject>CA1 Region, Hippocampal - physiology</subject><subject>Cognition</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Infralimbic cortex</subject><subject>Male</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neural Pathways - physiology</subject><subject>Neurons - physiology</subject><subject>Perirhinal Cortex - physiology</subject><subject>Prefrontal Cortex - physiology</subject><subject>Prelimbic cortex</subject><subject>Rats, Inbred F344</subject><subject>Temporal Lobe - physiology</subject><issn>0197-4580</issn><issn>1558-1497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqNkUGLFDEQhYMo7uzqX5A-ePDSbSWd7k5ABFndVVjwoueQTipjhu5kTDID--_NMOvi3jylIK9evaqPkLcUOgp0fL_rAh5SnH1c9NaHbceAig7GDph4RjZ0GERLuZyekw1QObV8EHBBLnPeAcDEp_EluegBeip7uiH42eccjdfzgg06h6bkJrpG26MOBm2jt9jE0OwTuhRD0UtjYire1EIH26xofS0LrvuYarHEufqEjOvJUJvij77cvyIvnF4yvn54r8jPmy8_rr-2d99vv11_umsNl0NpmevZ1FtJueYzSEYRORoHgxDGDL0dBxCUT8Dp7Di3I1DKwQlWd3bU4thfkY9n3_1hrskMhlJDqX3yq073Kmqvnv4E_0tt41GNgkkJshq8ezBI8fcBc1GrzwaXRQeMh6xYvSBlPXBRpR_OUpNizvU8j2MoqBMptVNPSakTKQWjqqRq-5t_oz42_0VTBTdnAdaDHT0mlY3HExOfKiVlo_-_SX8AhRavqg</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Hernandez, Abbi R.</creator><creator>Reasor, Jordan E.</creator><creator>Truckenbrod, Leah M.</creator><creator>Campos, Keila T.</creator><creator>Federico, Quinten P.</creator><creator>Fertal, Kaeli E.</creator><creator>Lubke, Katelyn N.</creator><creator>Johnson, Sarah A.</creator><creator>Clark, Benjamin J.</creator><creator>Maurer, Andrew. P.</creator><creator>Burke, Sara N.</creator><general>Elsevier Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20181001</creationdate><title>Dissociable effects of advanced age on prefrontal cortical and medial temporal lobe ensemble activity</title><author>Hernandez, Abbi R. ; Reasor, Jordan E. ; Truckenbrod, Leah M. ; Campos, Keila T. ; Federico, Quinten P. ; Fertal, Kaeli E. ; Lubke, Katelyn N. ; Johnson, Sarah A. ; Clark, Benjamin J. ; Maurer, Andrew. 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P.</au><au>Burke, Sara N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dissociable effects of advanced age on prefrontal cortical and medial temporal lobe ensemble activity</atitle><jtitle>Neurobiology of aging</jtitle><addtitle>Neurobiol Aging</addtitle><date>2018-10-01</date><risdate>2018</risdate><volume>70</volume><spage>217</spage><epage>232</epage><pages>217-232</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>The link between age-related cellular changes within brain regions and larger scale neuronal ensemble dynamics critical for cognition has not been fully elucidated. The present study measured neuron activity within medial prefrontal cortex (PFC), perirhinal cortex (PER), and hippocampal subregion CA1 of young and aged rats by labeling expression of the immediate-early gene Arc. The proportion of cells expressing Arc was quantified at baseline and after a behavior that requires these regions. In addition, PER and CA1 projection neurons to PFC were identified with retrograde labeling. Within CA1, no age-related differences in neuronal activity were observed in the entire neuron population or within CA1 pyramidal cells that project to PFC. Although behavior was comparable across age groups, behaviorally driven Arc expression was higher in the deep layers of both PER and PFC and lower in the superficial layers of these regions. Moreover, age-related changes in activity levels were most evident within PER cells that project to PFC. 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subjects | Aging - physiology Animals Arc Association Learning - physiology Behavior, Animal CA1 CA1 Region, Hippocampal - physiology Cognition Cytoskeletal Proteins - metabolism Infralimbic cortex Male Nerve Tissue Proteins - metabolism Neural Pathways - physiology Neurons - physiology Perirhinal Cortex - physiology Prefrontal Cortex - physiology Prelimbic cortex Rats, Inbred F344 Temporal Lobe - physiology |
title | Dissociable effects of advanced age on prefrontal cortical and medial temporal lobe ensemble activity |
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