Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse...
- Autores
- Litif, Carl G.; Flom, Levi T.; Sandum, Kathryn L.; Hodgins, Skylar L.; Vaccaro, Lucio; Stitzel, Jerry A.; Ungerleider, Nathan; Mannino, María Constanza; Gigley, Jason P.; Schoborg, Todd A.; Bobadilla, Ana Clara
- Año de publicación
- 2025
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Recurrent cocaine seeking is a hallmark of cocaine use disorder. To develop therapeutic targets, it is critical to understand the neurobiological changes specific to cocaine-seeking in context with the seeking of non-drug rewards, e.g., sucrose. The nucleus accumbens (NAc) and medial prefrontal cortex (mPFC) are known regions associated with cocaine- and sucrose-seeking ensembles, i.e., a sparse population of co-activated neurons linked with behavior. Within ensembles, transcriptomic alterations in the NAc and mPFC underlie the learning and recall of cocaine- and sucrose-seeking behavior. However, the transcriptomics exclusively driving cocaine seeking independent from sucrose seeking have not yet been defined using a within-subject approach. Using Ai14:cFos-TRAP2 transgenic mice in a dual cocaine and sucrose self-administration model, we fluorescently sorted and characterized the transcriptomes defining cocaine-seeking in reference to the sucrose-seeking ensemble, overlapping ensemble in between cocaine and sucrose-seeking, and the non-ensemble population. Our data suggests there are robust transcriptomic changes linked with cocaine-seeking that differ from sucroseseeking ensembles and the non-ensemble population which could guide future studies aimed to detangle cocaineseeking behavior without altering non-drug reward seeking.
Instituto de Investigaciones Bioquímicas de La Plata - Materia
-
Ciencias Médicas
Farmacia
Cocaine
Sucrose
Neuronal ensembles
RNAsequencing - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/4.0/
- Repositorio
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/189513
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Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse modelLitif, Carl G.Flom, Levi T.Sandum, Kathryn L.Hodgins, Skylar L.Vaccaro, LucioStitzel, Jerry A.Ungerleider, NathanMannino, María ConstanzaGigley, Jason P.Schoborg, Todd A.Bobadilla, Ana ClaraCiencias MédicasFarmaciaCocaineSucroseNeuronal ensemblesRNAsequencingRecurrent cocaine seeking is a hallmark of cocaine use disorder. To develop therapeutic targets, it is critical to understand the neurobiological changes specific to cocaine-seeking in context with the seeking of non-drug rewards, e.g., sucrose. The nucleus accumbens (NAc) and medial prefrontal cortex (mPFC) are known regions associated with cocaine- and sucrose-seeking ensembles, i.e., a sparse population of co-activated neurons linked with behavior. Within ensembles, transcriptomic alterations in the NAc and mPFC underlie the learning and recall of cocaine- and sucrose-seeking behavior. However, the transcriptomics exclusively driving cocaine seeking independent from sucrose seeking have not yet been defined using a within-subject approach. Using Ai14:cFos-TRAP2 transgenic mice in a dual cocaine and sucrose self-administration model, we fluorescently sorted and characterized the transcriptomes defining cocaine-seeking in reference to the sucrose-seeking ensemble, overlapping ensemble in between cocaine and sucrose-seeking, and the non-ensemble population. Our data suggests there are robust transcriptomic changes linked with cocaine-seeking that differ from sucroseseeking ensembles and the non-ensemble population which could guide future studies aimed to detangle cocaineseeking behavior without altering non-drug reward seeking.Instituto de Investigaciones Bioquímicas de La Plata2025-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/189513enginfo:eu-repo/semantics/altIdentifier/issn/2772-3925info:eu-repo/semantics/altIdentifier/doi/10.1016/j.addicn.2025.100242info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2026-03-26T09:20:51Zoai:sedici.unlp.edu.ar:10915/189513Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292026-03-26 09:20:51.918SEDICI (UNLP) - Universidad Nacional de La Platafalse |
| dc.title.none.fl_str_mv |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model |
| title |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model |
| spellingShingle |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model Litif, Carl G. Ciencias Médicas Farmacia Cocaine Sucrose Neuronal ensembles RNAsequencing |
| title_short |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model |
| title_full |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model |
| title_fullStr |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model |
| title_full_unstemmed |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model |
| title_sort |
Corticostriatal cocaine-seeking ensembles are defined by differing gene expression from sucrose-seeking ensembles using a within-subject dual self-administration and seeking mouse model |
| dc.creator.none.fl_str_mv |
Litif, Carl G. Flom, Levi T. Sandum, Kathryn L. Hodgins, Skylar L. Vaccaro, Lucio Stitzel, Jerry A. Ungerleider, Nathan Mannino, María Constanza Gigley, Jason P. Schoborg, Todd A. Bobadilla, Ana Clara |
| author |
Litif, Carl G. |
| author_facet |
Litif, Carl G. Flom, Levi T. Sandum, Kathryn L. Hodgins, Skylar L. Vaccaro, Lucio Stitzel, Jerry A. Ungerleider, Nathan Mannino, María Constanza Gigley, Jason P. Schoborg, Todd A. Bobadilla, Ana Clara |
| author_role |
author |
| author2 |
Flom, Levi T. Sandum, Kathryn L. Hodgins, Skylar L. Vaccaro, Lucio Stitzel, Jerry A. Ungerleider, Nathan Mannino, María Constanza Gigley, Jason P. Schoborg, Todd A. Bobadilla, Ana Clara |
| author2_role |
author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Ciencias Médicas Farmacia Cocaine Sucrose Neuronal ensembles RNAsequencing |
| topic |
Ciencias Médicas Farmacia Cocaine Sucrose Neuronal ensembles RNAsequencing |
| dc.description.none.fl_txt_mv |
Recurrent cocaine seeking is a hallmark of cocaine use disorder. To develop therapeutic targets, it is critical to understand the neurobiological changes specific to cocaine-seeking in context with the seeking of non-drug rewards, e.g., sucrose. The nucleus accumbens (NAc) and medial prefrontal cortex (mPFC) are known regions associated with cocaine- and sucrose-seeking ensembles, i.e., a sparse population of co-activated neurons linked with behavior. Within ensembles, transcriptomic alterations in the NAc and mPFC underlie the learning and recall of cocaine- and sucrose-seeking behavior. However, the transcriptomics exclusively driving cocaine seeking independent from sucrose seeking have not yet been defined using a within-subject approach. Using Ai14:cFos-TRAP2 transgenic mice in a dual cocaine and sucrose self-administration model, we fluorescently sorted and characterized the transcriptomes defining cocaine-seeking in reference to the sucrose-seeking ensemble, overlapping ensemble in between cocaine and sucrose-seeking, and the non-ensemble population. Our data suggests there are robust transcriptomic changes linked with cocaine-seeking that differ from sucroseseeking ensembles and the non-ensemble population which could guide future studies aimed to detangle cocaineseeking behavior without altering non-drug reward seeking. Instituto de Investigaciones Bioquímicas de La Plata |
| description |
Recurrent cocaine seeking is a hallmark of cocaine use disorder. To develop therapeutic targets, it is critical to understand the neurobiological changes specific to cocaine-seeking in context with the seeking of non-drug rewards, e.g., sucrose. The nucleus accumbens (NAc) and medial prefrontal cortex (mPFC) are known regions associated with cocaine- and sucrose-seeking ensembles, i.e., a sparse population of co-activated neurons linked with behavior. Within ensembles, transcriptomic alterations in the NAc and mPFC underlie the learning and recall of cocaine- and sucrose-seeking behavior. However, the transcriptomics exclusively driving cocaine seeking independent from sucrose seeking have not yet been defined using a within-subject approach. Using Ai14:cFos-TRAP2 transgenic mice in a dual cocaine and sucrose self-administration model, we fluorescently sorted and characterized the transcriptomes defining cocaine-seeking in reference to the sucrose-seeking ensemble, overlapping ensemble in between cocaine and sucrose-seeking, and the non-ensemble population. Our data suggests there are robust transcriptomic changes linked with cocaine-seeking that differ from sucroseseeking ensembles and the non-ensemble population which could guide future studies aimed to detangle cocaineseeking behavior without altering non-drug reward seeking. |
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2025 |
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2025-11 |
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eng |
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