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Effects of Cannabidiol in post-stroke mood disorders in neonatal rats.

dc.contributor.authorVilla, María
dc.contributor.authorMartínez Orgado, José Antonio
dc.date.accessioned2025-03-06T07:50:30Z
dc.date.available2025-03-06T07:50:30Z
dc.date.issued2024-02-15
dc.description.abstractBackground: Neonatal rats can manifest post-stroke mood disorders (PSMD) following middle cerebral artery occlusion (MCAO). We investigated whether cannabidiol (CBD) neuroprotection, previously demonstrated in neonatal rats after MCAO, includes prevention of PSMD development. Methods: Seven-day-old Wistar rats (P7) underwent MCAO and received either vehicle or 5 mg/kg CBD treatment. Brain damage was quantified by MRI, and neurobehavioral and histological (TUNEL) studies were performed at P14 and P37. PSMD were assessed using the tail suspension test, forced swimming test, and open field tests. The dopaminergic system was evaluated by quantifying dopaminergic neurons (TH+) in the Ventral Tegmental Area (VTA), measuring brain dopamine (DA) concentration and DA transporter expression, and assessing the expression and function D2 receptors (D2R) through [35S]GTPγS binding. Animals without MCAO served as controls. Results: CBD reduced MCAO-induced brain damage and improved motor performance. At P14, MCAO induced depressive-like behavior, characterized by reduced TH+ cell population and DA levels, which CBD did not prevent. However, CBD ameliorated hyperactivity observed at P37, preventing increased DA concentration by restoring D2R function. Conclusions: These findings confirm the development of PSMD following MCAO in neonatal rats and highlight CBD as a neuroprotective agent capable of long-term functional normalization of the dopaminergic system post-MCAO. Impact: MCAO in neonatal rats led to post-stroke mood disorders consisting in a depression-like picture in the medium term evolving towards long-term hyperactivity, associated with an alteration of the dopaminergic system. The administration of CBD after MCAO did not prevent the development of depressive-like behavior, but reduced long-term hyperactivity, normalizing dopamine receptor function. These data point to the importance of considering the development of depression-like symptoms after neonatal stroke, a well-known complication after stroke in adults. Our work confirms the interest of CBD as a possible treatment for neonatal stroke.
dc.description.departmentDepto. de Salud Pública y Materno - Infantil
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.statuspub
dc.identifier.citationVilla M, Martínez-Vega M, Silva L, Muneta-Arrate I, Gómez-Soria A, Muguruza C, Del Pozo A, de Hoz-Rivera M, Romero A, Callado LF, Casarejos MJ, Martínez-Orgado J. Effects of cannabidiol in post-stroke mood disorders in neonatal rats. Pediatr Res. 2024 Jun;95(7):1783-1790. doi: 10.1038/s41390-024-03077-8.
dc.identifier.doi10.1038/s41390-024-03077-8
dc.identifier.essn1530-0447
dc.identifier.issn0031-3998
dc.identifier.officialurlhttps://doi.org/10.1038/s41390-024-03077-8
dc.identifier.pmid38360979
dc.identifier.relatedurlhttps://www.nature.com/articles/s41390-024-03077-8
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/38360979/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/118548
dc.issue.number7
dc.journal.titlePediatric Res
dc.language.isoeng
dc.page.final1790
dc.page.initial1783
dc.publisherSpringer Nature
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/Plan Nacional de R+D+I, AES 2017-2020/PI19/ 00927
dc.relation.projectIDPID2019-106404RB-I00
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/Plan Nacional de R+D+I, AES 2021-2023/RD21/0012/0023
dc.rights.accessRightsrestricted access
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco24 Ciencias de la Vida
dc.titleEffects of Cannabidiol in post-stroke mood disorders in neonatal rats.
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number95
dspace.entity.typePublication
relation.isAuthorOfPublication03162d7f-e1e1-4b51-b7ec-e20adaf7c220
relation.isAuthorOfPublication.latestForDiscovery03162d7f-e1e1-4b51-b7ec-e20adaf7c220

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