Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei
- Autores
- Esparza, Maria Alejandra; Bollati, Flavia Andrea; Garcia Keller, Constanza; Virgolini, Miriam Beatriz; Lopez, Lidia Margarita; Brusco, Herminia Alicia; Shen, Hao Wei; Kalivas, Peter W.; Cancela, Liliana Marina
- Año de publicación
- 2012
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- This study investigated whether the adaptations induced by repeated cocaine in the actin cytoskeleton, the surface expression of AMPA receptor subunit GluR1, dendritic spine morphology and the size of postsynaptic density (PSD) in nucleus accumbens (NAc) and prefrontal cortex (Pfc) are relevant to how repeated immobilization stress induces behavioural cross-sensitization to cocaine. Wistar rats were restrained daily (2 hours) for 7 days, and three weeks later, the NAc and Pfc were dissected from animals 45 min following acute saline or cocaine (30 mg/kg i.p.). F-actin, actin-binding protein (ABP) and GluR1 were determined by western blotting, and dendritic spines and the size of PSD measured by electron microscopy. In the NAc, a decrease in p-cofilin and p-cortactin, and an increase in GluR1 and PSD size was found in the stress plus cocaine group, while in the Pfc an increase in F-actin and Arp2, as well as the number of spines, was observed in the stress group. Inhibition of actin cycling with latrunculin A in NAc restored expression of GluR1, and both latrunculin A and the AMPAR antagonist CNQX inhibited the expression of motor cross-sensitization to cocaine (15 mg/kg i.p.). This study shows that cross-sensitization is associated with changes in the actin cytoskeleton, the size of the PSD and GluR1 expression that partly parallel the neuroadaptations elicited by sensitization to repeated cocaine. Also, the actin dynamics regulating GluR1 expression in the NAc contribute to the expression of cross-sensitization between stress and cocaine, but the changes in Pfc were not associated with cross-sensitization.
Fil: Esparza, Maria Alejandra. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina
Fil: Bollati, Flavia Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina
Fil: Garcia Keller, Constanza. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina
Fil: Virgolini, Miriam Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina
Fil: Lopez, Lidia Margarita. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; Argentina
Fil: Brusco, Herminia Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; Argentina
Fil: Shen, Hao Wei. Medical University of South Carolina; Estados Unidos
Fil: Kalivas, Peter W.. Medical University of South Carolina; Estados Unidos
Fil: Cancela, Liliana Marina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina - Materia
-
F-actin
dendritic spines
AMPA receptors
latrunculin A - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/274395
Ver los metadatos del registro completo
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Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nucleiEsparza, Maria AlejandraBollati, Flavia AndreaGarcia Keller, ConstanzaVirgolini, Miriam BeatrizLopez, Lidia MargaritaBrusco, Herminia AliciaShen, Hao WeiKalivas, Peter W.Cancela, Liliana MarinaF-actindendritic spinesAMPA receptorslatrunculin Ahttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3This study investigated whether the adaptations induced by repeated cocaine in the actin cytoskeleton, the surface expression of AMPA receptor subunit GluR1, dendritic spine morphology and the size of postsynaptic density (PSD) in nucleus accumbens (NAc) and prefrontal cortex (Pfc) are relevant to how repeated immobilization stress induces behavioural cross-sensitization to cocaine. Wistar rats were restrained daily (2 hours) for 7 days, and three weeks later, the NAc and Pfc were dissected from animals 45 min following acute saline or cocaine (30 mg/kg i.p.). F-actin, actin-binding protein (ABP) and GluR1 were determined by western blotting, and dendritic spines and the size of PSD measured by electron microscopy. In the NAc, a decrease in p-cofilin and p-cortactin, and an increase in GluR1 and PSD size was found in the stress plus cocaine group, while in the Pfc an increase in F-actin and Arp2, as well as the number of spines, was observed in the stress group. Inhibition of actin cycling with latrunculin A in NAc restored expression of GluR1, and both latrunculin A and the AMPAR antagonist CNQX inhibited the expression of motor cross-sensitization to cocaine (15 mg/kg i.p.). This study shows that cross-sensitization is associated with changes in the actin cytoskeleton, the size of the PSD and GluR1 expression that partly parallel the neuroadaptations elicited by sensitization to repeated cocaine. Also, the actin dynamics regulating GluR1 expression in the NAc contribute to the expression of cross-sensitization between stress and cocaine, but the changes in Pfc were not associated with cross-sensitization.Fil: Esparza, Maria Alejandra. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; ArgentinaFil: Bollati, Flavia Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; ArgentinaFil: Garcia Keller, Constanza. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; ArgentinaFil: Virgolini, Miriam Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; ArgentinaFil: Lopez, Lidia Margarita. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Brusco, Herminia Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Shen, Hao Wei. Medical University of South Carolina; Estados UnidosFil: Kalivas, Peter W.. Medical University of South Carolina; Estados UnidosFil: Cancela, Liliana Marina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; ArgentinaWiley Blackwell Publishing, Inc2012-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/274395Esparza, Maria Alejandra; Bollati, Flavia Andrea; Garcia Keller, Constanza; Virgolini, Miriam Beatriz; Lopez, Lidia Margarita; et al.; Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei; Wiley Blackwell Publishing, Inc; European Journal of Neuroscience; 36; 8; 6-2012; 3103-31170953-816XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1111/j.1460-9568.2012.08239.xinfo:eu-repo/semantics/altIdentifier/doi/10.1111/j.1460-9568.2012.08239.xinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T10:21:45Zoai:ri.conicet.gov.ar:11336/274395instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-11-05 10:21:45.936CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei |
| title |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei |
| spellingShingle |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei Esparza, Maria Alejandra F-actin dendritic spines AMPA receptors latrunculin A |
| title_short |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei |
| title_full |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei |
| title_fullStr |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei |
| title_full_unstemmed |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei |
| title_sort |
Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei |
| dc.creator.none.fl_str_mv |
Esparza, Maria Alejandra Bollati, Flavia Andrea Garcia Keller, Constanza Virgolini, Miriam Beatriz Lopez, Lidia Margarita Brusco, Herminia Alicia Shen, Hao Wei Kalivas, Peter W. Cancela, Liliana Marina |
| author |
Esparza, Maria Alejandra |
| author_facet |
Esparza, Maria Alejandra Bollati, Flavia Andrea Garcia Keller, Constanza Virgolini, Miriam Beatriz Lopez, Lidia Margarita Brusco, Herminia Alicia Shen, Hao Wei Kalivas, Peter W. Cancela, Liliana Marina |
| author_role |
author |
| author2 |
Bollati, Flavia Andrea Garcia Keller, Constanza Virgolini, Miriam Beatriz Lopez, Lidia Margarita Brusco, Herminia Alicia Shen, Hao Wei Kalivas, Peter W. Cancela, Liliana Marina |
| author2_role |
author author author author author author author author |
| dc.subject.none.fl_str_mv |
F-actin dendritic spines AMPA receptors latrunculin A |
| topic |
F-actin dendritic spines AMPA receptors latrunculin A |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
| dc.description.none.fl_txt_mv |
This study investigated whether the adaptations induced by repeated cocaine in the actin cytoskeleton, the surface expression of AMPA receptor subunit GluR1, dendritic spine morphology and the size of postsynaptic density (PSD) in nucleus accumbens (NAc) and prefrontal cortex (Pfc) are relevant to how repeated immobilization stress induces behavioural cross-sensitization to cocaine. Wistar rats were restrained daily (2 hours) for 7 days, and three weeks later, the NAc and Pfc were dissected from animals 45 min following acute saline or cocaine (30 mg/kg i.p.). F-actin, actin-binding protein (ABP) and GluR1 were determined by western blotting, and dendritic spines and the size of PSD measured by electron microscopy. In the NAc, a decrease in p-cofilin and p-cortactin, and an increase in GluR1 and PSD size was found in the stress plus cocaine group, while in the Pfc an increase in F-actin and Arp2, as well as the number of spines, was observed in the stress group. Inhibition of actin cycling with latrunculin A in NAc restored expression of GluR1, and both latrunculin A and the AMPAR antagonist CNQX inhibited the expression of motor cross-sensitization to cocaine (15 mg/kg i.p.). This study shows that cross-sensitization is associated with changes in the actin cytoskeleton, the size of the PSD and GluR1 expression that partly parallel the neuroadaptations elicited by sensitization to repeated cocaine. Also, the actin dynamics regulating GluR1 expression in the NAc contribute to the expression of cross-sensitization between stress and cocaine, but the changes in Pfc were not associated with cross-sensitization. Fil: Esparza, Maria Alejandra. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina Fil: Bollati, Flavia Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina Fil: Garcia Keller, Constanza. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina Fil: Virgolini, Miriam Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina Fil: Lopez, Lidia Margarita. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; Argentina Fil: Brusco, Herminia Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; Argentina Fil: Shen, Hao Wei. Medical University of South Carolina; Estados Unidos Fil: Kalivas, Peter W.. Medical University of South Carolina; Estados Unidos Fil: Cancela, Liliana Marina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Farmacología Experimental de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Farmacología Experimental de Córdoba; Argentina |
| description |
This study investigated whether the adaptations induced by repeated cocaine in the actin cytoskeleton, the surface expression of AMPA receptor subunit GluR1, dendritic spine morphology and the size of postsynaptic density (PSD) in nucleus accumbens (NAc) and prefrontal cortex (Pfc) are relevant to how repeated immobilization stress induces behavioural cross-sensitization to cocaine. Wistar rats were restrained daily (2 hours) for 7 days, and three weeks later, the NAc and Pfc were dissected from animals 45 min following acute saline or cocaine (30 mg/kg i.p.). F-actin, actin-binding protein (ABP) and GluR1 were determined by western blotting, and dendritic spines and the size of PSD measured by electron microscopy. In the NAc, a decrease in p-cofilin and p-cortactin, and an increase in GluR1 and PSD size was found in the stress plus cocaine group, while in the Pfc an increase in F-actin and Arp2, as well as the number of spines, was observed in the stress group. Inhibition of actin cycling with latrunculin A in NAc restored expression of GluR1, and both latrunculin A and the AMPAR antagonist CNQX inhibited the expression of motor cross-sensitization to cocaine (15 mg/kg i.p.). This study shows that cross-sensitization is associated with changes in the actin cytoskeleton, the size of the PSD and GluR1 expression that partly parallel the neuroadaptations elicited by sensitization to repeated cocaine. Also, the actin dynamics regulating GluR1 expression in the NAc contribute to the expression of cross-sensitization between stress and cocaine, but the changes in Pfc were not associated with cross-sensitization. |
| publishDate |
2012 |
| dc.date.none.fl_str_mv |
2012-06 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/274395 Esparza, Maria Alejandra; Bollati, Flavia Andrea; Garcia Keller, Constanza; Virgolini, Miriam Beatriz; Lopez, Lidia Margarita; et al.; Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei; Wiley Blackwell Publishing, Inc; European Journal of Neuroscience; 36; 8; 6-2012; 3103-3117 0953-816X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/274395 |
| identifier_str_mv |
Esparza, Maria Alejandra; Bollati, Flavia Andrea; Garcia Keller, Constanza; Virgolini, Miriam Beatriz; Lopez, Lidia Margarita; et al.; Stress‐induced sensitization to cocaine: actin cytoskeleton remodeling within mesocorticolimbic nuclei; Wiley Blackwell Publishing, Inc; European Journal of Neuroscience; 36; 8; 6-2012; 3103-3117 0953-816X CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
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info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1111/j.1460-9568.2012.08239.x info:eu-repo/semantics/altIdentifier/doi/10.1111/j.1460-9568.2012.08239.x |
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openAccess |
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Wiley Blackwell Publishing, Inc |
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Wiley Blackwell Publishing, Inc |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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