The sinking platform test: a novel paradigm to measure persistence in animal models
Persistence is the propensity to maintain goal-directed actions despite adversities. While this temperamental trait is crucial to mitigate depression risk, its neurobiological foundations remain elusive. Developing behavioral tasks to capture persistence in animal models is crucial for understanding...
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Veröffentlicht in: | Neuropsychopharmacology (New York, N.Y.) N.Y.), 2024-08, Vol.49 (9), p.1373-1382 |
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description | Persistence is the propensity to maintain goal-directed actions despite adversities. While this temperamental trait is crucial to mitigate depression risk, its neurobiological foundations remain elusive. Developing behavioral tasks to capture persistence in animal models is crucial for understanding its molecular underpinnings. Here, we introduce the Sinking Platform Test (SPT), a novel high-throughput paradigm to measure persistence. Mice were trained to exit a water-filled tank by ascending onto a platform above water level. Throughout the training, mice were also occasionally exposed to "failure trials," during which an operator would submerge a platform right after the mouse climbed onto it, requiring the mouse to reach and ascend a newly introduced platform. Following training, mice were subjected to a 5-min test exclusively consisting of failure trials. Male and female mice exhibited comparable persistence, measured by the number of climbed platforms during the test. Furthermore, this index was increased by chronic administration of fluoxetine or imipramine; conversely, it was reduced by acute and chronic haloperidol. Notably, six weeks of social isolation reduced SPT performance, and this effect was rescued by imipramine treatment over the last two weeks. A 4-week regimen of voluntary wheel running also improved persistence in socially isolated mice. Finally, comparing transcriptomic profiles of the prefrontal cortex of mice with high and low SPT performance revealed significant enrichment of immediate-early genes known to shape susceptibility for chronic stress. These findings highlight the potential of SPT as a promising method to uncover the biological mechanisms of persistence and evaluate novel interventions to enhance this response. |
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While this temperamental trait is crucial to mitigate depression risk, its neurobiological foundations remain elusive. Developing behavioral tasks to capture persistence in animal models is crucial for understanding its molecular underpinnings. Here, we introduce the Sinking Platform Test (SPT), a novel high-throughput paradigm to measure persistence. Mice were trained to exit a water-filled tank by ascending onto a platform above water level. Throughout the training, mice were also occasionally exposed to "failure trials," during which an operator would submerge a platform right after the mouse climbed onto it, requiring the mouse to reach and ascend a newly introduced platform. Following training, mice were subjected to a 5-min test exclusively consisting of failure trials. Male and female mice exhibited comparable persistence, measured by the number of climbed platforms during the test. Furthermore, this index was increased by chronic administration of fluoxetine or imipramine; conversely, it was reduced by acute and chronic haloperidol. Notably, six weeks of social isolation reduced SPT performance, and this effect was rescued by imipramine treatment over the last two weeks. A 4-week regimen of voluntary wheel running also improved persistence in socially isolated mice. Finally, comparing transcriptomic profiles of the prefrontal cortex of mice with high and low SPT performance revealed significant enrichment of immediate-early genes known to shape susceptibility for chronic stress. These findings highlight the potential of SPT as a promising method to uncover the biological mechanisms of persistence and evaluate novel interventions to enhance this response.</description><identifier>ISSN: 0893-133X</identifier><identifier>ISSN: 1740-634X</identifier><identifier>EISSN: 1740-634X</identifier><identifier>DOI: 10.1038/s41386-024-01827-0</identifier><identifier>PMID: 38396257</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject>Animal models ; Animals ; Behavior, Animal - drug effects ; Behavior, Animal - physiology ; Disease Models, Animal ; Female ; Fluoxetine ; Fluoxetine - pharmacology ; Haloperidol ; Haloperidol - pharmacology ; Imipramine ; Imipramine - pharmacology ; Immediate-early proteins ; Male ; Mice ; Mice, Inbred C57BL ; Molecular modelling ; Prefrontal cortex ; Prefrontal Cortex - drug effects ; Prefrontal Cortex - metabolism ; Prefrontal Cortex - physiology ; Social interactions ; Social isolation ; Social Isolation - psychology ; Transcriptomics ; Water levels ; Wheel running</subject><ispartof>Neuropsychopharmacology (New York, N.Y.), 2024-08, Vol.49 (9), p.1373-1382</ispartof><rights>2024. The Author(s), under exclusive licence to American College of Neuropsychopharmacology.</rights><rights>The Author(s), under exclusive licence to American College of Neuropsychopharmacology 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c282t-b1c616b0251e004a9fa4e1d66ea4f967754e6b60dc643e7afe81e7121d1855903</cites><orcidid>0000-0002-4498-9637 ; 0000-0002-5818-774X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38396257$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Floris, Gabriele</creatorcontrib><creatorcontrib>Godar, Sean C</creatorcontrib><creatorcontrib>Braccagni, Giulia</creatorcontrib><creatorcontrib>Piras, Ignazio S</creatorcontrib><creatorcontrib>Ravens, Alicia</creatorcontrib><creatorcontrib>Zanda, Mary T</creatorcontrib><creatorcontrib>Huentelman, Matthew J</creatorcontrib><creatorcontrib>Bortolato, Marco</creatorcontrib><title>The sinking platform test: a novel paradigm to measure persistence in animal models</title><title>Neuropsychopharmacology (New York, N.Y.)</title><addtitle>Neuropsychopharmacology</addtitle><description>Persistence is the propensity to maintain goal-directed actions despite adversities. While this temperamental trait is crucial to mitigate depression risk, its neurobiological foundations remain elusive. Developing behavioral tasks to capture persistence in animal models is crucial for understanding its molecular underpinnings. Here, we introduce the Sinking Platform Test (SPT), a novel high-throughput paradigm to measure persistence. Mice were trained to exit a water-filled tank by ascending onto a platform above water level. Throughout the training, mice were also occasionally exposed to "failure trials," during which an operator would submerge a platform right after the mouse climbed onto it, requiring the mouse to reach and ascend a newly introduced platform. Following training, mice were subjected to a 5-min test exclusively consisting of failure trials. Male and female mice exhibited comparable persistence, measured by the number of climbed platforms during the test. Furthermore, this index was increased by chronic administration of fluoxetine or imipramine; conversely, it was reduced by acute and chronic haloperidol. Notably, six weeks of social isolation reduced SPT performance, and this effect was rescued by imipramine treatment over the last two weeks. A 4-week regimen of voluntary wheel running also improved persistence in socially isolated mice. Finally, comparing transcriptomic profiles of the prefrontal cortex of mice with high and low SPT performance revealed significant enrichment of immediate-early genes known to shape susceptibility for chronic stress. These findings highlight the potential of SPT as a promising method to uncover the biological mechanisms of persistence and evaluate novel interventions to enhance this response.</description><subject>Animal models</subject><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Behavior, Animal - physiology</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Fluoxetine</subject><subject>Fluoxetine - pharmacology</subject><subject>Haloperidol</subject><subject>Haloperidol - pharmacology</subject><subject>Imipramine</subject><subject>Imipramine - pharmacology</subject><subject>Immediate-early proteins</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Molecular modelling</subject><subject>Prefrontal cortex</subject><subject>Prefrontal Cortex - drug effects</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Prefrontal Cortex - physiology</subject><subject>Social interactions</subject><subject>Social isolation</subject><subject>Social Isolation - psychology</subject><subject>Transcriptomics</subject><subject>Water levels</subject><subject>Wheel running</subject><issn>0893-133X</issn><issn>1740-634X</issn><issn>1740-634X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE1LxDAQhoMoun78AQ8S8OKlOpOkSepNxC8QPLjC3kK2nWq1Xyat4L-366oHTwPDMy_vPIwdIpwiSHsWFUqrExAqAbTCJLDBZmgUJFqqxSabgc1kglIudthujK8AmBptt9mOtDLTIjUz9jh_IR6r9q1qn3lf-6HsQsMHisM597ztPqjmvQ--qJ6ndccb8nEMxHsKsYoDtTnxquW-rRpf86YrqI77bKv0daSDn7nHnq6v5pe3yf3Dzd3lxX2SCyuGZIm5Rr0EkSIBKJ-VXhEWWpNXZaaNSRXppYYi10qS8SVZJIMCC7RpmoHcYyfr3D507-NU2TVVzKmufUvdGJ0Ei8JYlaUTevwPfe3G0E7tVhRYk2Z6RYk1lYcuxkCl68P0V_h0CG6l3K2Vu0m5-1buVi2OfqLHZUPF38mvY_kFSRt7ZQ</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Floris, Gabriele</creator><creator>Godar, Sean C</creator><creator>Braccagni, Giulia</creator><creator>Piras, Ignazio S</creator><creator>Ravens, Alicia</creator><creator>Zanda, Mary T</creator><creator>Huentelman, Matthew J</creator><creator>Bortolato, Marco</creator><general>Nature Publishing Group</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>7TK</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4498-9637</orcidid><orcidid>https://orcid.org/0000-0002-5818-774X</orcidid></search><sort><creationdate>20240801</creationdate><title>The sinking platform test: a novel paradigm to measure persistence in animal models</title><author>Floris, Gabriele ; Godar, Sean C ; Braccagni, Giulia ; Piras, Ignazio S ; Ravens, Alicia ; Zanda, Mary T ; Huentelman, Matthew J ; Bortolato, Marco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-b1c616b0251e004a9fa4e1d66ea4f967754e6b60dc643e7afe81e7121d1855903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Behavior, Animal - physiology</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Fluoxetine</topic><topic>Fluoxetine - pharmacology</topic><topic>Haloperidol</topic><topic>Haloperidol - pharmacology</topic><topic>Imipramine</topic><topic>Imipramine - pharmacology</topic><topic>Immediate-early proteins</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Molecular modelling</topic><topic>Prefrontal cortex</topic><topic>Prefrontal Cortex - drug effects</topic><topic>Prefrontal Cortex - metabolism</topic><topic>Prefrontal Cortex - physiology</topic><topic>Social interactions</topic><topic>Social isolation</topic><topic>Social Isolation - psychology</topic><topic>Transcriptomics</topic><topic>Water levels</topic><topic>Wheel running</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Floris, Gabriele</creatorcontrib><creatorcontrib>Godar, Sean C</creatorcontrib><creatorcontrib>Braccagni, Giulia</creatorcontrib><creatorcontrib>Piras, Ignazio S</creatorcontrib><creatorcontrib>Ravens, Alicia</creatorcontrib><creatorcontrib>Zanda, Mary T</creatorcontrib><creatorcontrib>Huentelman, Matthew J</creatorcontrib><creatorcontrib>Bortolato, Marco</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Floris, Gabriele</au><au>Godar, Sean C</au><au>Braccagni, Giulia</au><au>Piras, Ignazio S</au><au>Ravens, Alicia</au><au>Zanda, Mary T</au><au>Huentelman, Matthew J</au><au>Bortolato, Marco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The sinking platform test: a novel paradigm to measure persistence in animal models</atitle><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle><addtitle>Neuropsychopharmacology</addtitle><date>2024-08-01</date><risdate>2024</risdate><volume>49</volume><issue>9</issue><spage>1373</spage><epage>1382</epage><pages>1373-1382</pages><issn>0893-133X</issn><issn>1740-634X</issn><eissn>1740-634X</eissn><abstract>Persistence is the propensity to maintain goal-directed actions despite adversities. While this temperamental trait is crucial to mitigate depression risk, its neurobiological foundations remain elusive. Developing behavioral tasks to capture persistence in animal models is crucial for understanding its molecular underpinnings. Here, we introduce the Sinking Platform Test (SPT), a novel high-throughput paradigm to measure persistence. Mice were trained to exit a water-filled tank by ascending onto a platform above water level. Throughout the training, mice were also occasionally exposed to "failure trials," during which an operator would submerge a platform right after the mouse climbed onto it, requiring the mouse to reach and ascend a newly introduced platform. Following training, mice were subjected to a 5-min test exclusively consisting of failure trials. Male and female mice exhibited comparable persistence, measured by the number of climbed platforms during the test. Furthermore, this index was increased by chronic administration of fluoxetine or imipramine; conversely, it was reduced by acute and chronic haloperidol. Notably, six weeks of social isolation reduced SPT performance, and this effect was rescued by imipramine treatment over the last two weeks. A 4-week regimen of voluntary wheel running also improved persistence in socially isolated mice. Finally, comparing transcriptomic profiles of the prefrontal cortex of mice with high and low SPT performance revealed significant enrichment of immediate-early genes known to shape susceptibility for chronic stress. 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subjects | Animal models Animals Behavior, Animal - drug effects Behavior, Animal - physiology Disease Models, Animal Female Fluoxetine Fluoxetine - pharmacology Haloperidol Haloperidol - pharmacology Imipramine Imipramine - pharmacology Immediate-early proteins Male Mice Mice, Inbred C57BL Molecular modelling Prefrontal cortex Prefrontal Cortex - drug effects Prefrontal Cortex - metabolism Prefrontal Cortex - physiology Social interactions Social isolation Social Isolation - psychology Transcriptomics Water levels Wheel running |
title | The sinking platform test: a novel paradigm to measure persistence in animal models |
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