Publication: Acylethanolamides and endocannabinoid signaling system in dorsal striatum of rats exposed to perinatal asphyxia.
dc.contributor.author | Holubiec, Mariana I | |
dc.contributor.author | Romero, Juan I | |
dc.contributor.author | Blanco, Eduardo | |
dc.contributor.author | Tornatore, Tamara Logica | |
dc.contributor.author | Suarez, Juan | |
dc.contributor.author | Rodriguez-de-Fonseca, Fernando | |
dc.contributor.author | Galeano, Pablo | |
dc.contributor.author | Capani, Francisco | |
dc.date.accessioned | 2023-01-25T09:47:04Z | |
dc.date.available | 2023-01-25T09:47:04Z | |
dc.date.issued | 2017-06-01 | |
dc.description.abstract | Endocannabinoids (eCBs) and acylethanolamides (AEs) have lately received more attention due to their neuroprotective functions in neurological disorders. Here we analyze the alterations induced by perinatal asphyxia (PA) in the main metabolic enzymes and receptors of the eCBs/AEs in the dorsal striatum of rats. To induce PA, we used a model developed by Bjelke et al. (1991). Immunohistochemical techniques were carried out to determine the expression of neuronal and glial markers (NeuN and GFAP), eCBs/AEs synthesis and degradation enzymes (DAGLα, NAPE-PLD and FAAH) and their receptors (CB1 and PPARα). We found a decrease in NAPE-PLD and PPARα expression. Since NAPE-PLD and PPARα take part in the production and reception of biochemical actions of AEs, such as oleoylethanolamide, these results may suggest that PA plays a key role in the regulation of this system. These data agree with previous results obtained in the hippocampus and encourage us to develop further studies using AEs as potential neuroprotective compounds. | |
dc.description.version | Si | |
dc.identifier.citation | Holubiec MI, Romero JI, Blanco E, Tornatore TL, Suarez J, Rodríguez de Fonseca F, et al. Acylethanolamides and endocannabinoid signaling system in dorsal striatum of rats exposed to perinatal asphyxia. Neurosci Lett. 2017 Jul 13;653:269-275 | |
dc.identifier.doi | 10.1016/j.neulet.2017.05.068 | |
dc.identifier.essn | 1872-7972 | |
dc.identifier.pmid | 28579484 | |
dc.identifier.unpaywallURL | https://ri.conicet.gov.ar/bitstream/11336/38529/5/CONICET_Digital_Nro.9fe6dfed-20fc-4ed3-8d52-a23cd466caea_D.pdf | |
dc.identifier.uri | http://hdl.handle.net/10668/11271 | |
dc.journal.title | Neuroscience letters | |
dc.journal.titleabbreviation | Neurosci Lett | |
dc.language.iso | en | |
dc.organization | Instituto de Investigación Biomédica de Málaga-IBIMA | |
dc.organization | Hospital Universitario Regional de Málaga | |
dc.page.number | 269-275 | |
dc.provenance | Realizada la curación de contenido 21/02/2025 | |
dc.publisher | Elsevier | |
dc.pubmedtype | Journal Article | |
dc.relation.publisherversion | https://linkinghub.elsevier.com/retrieve/pii/S0304-3940(17)30474-3 | |
dc.rights.accessRights | Restricted Access | |
dc.subject | CB1 | |
dc.subject | DAGLα | |
dc.subject | Dorsal striatum | |
dc.subject | NAPE-PLD | |
dc.subject | PPARα | |
dc.subject | Perinatal asphyxia | |
dc.subject.decs | Receptores activados del proliferador del peroxisoma | |
dc.subject.decs | Enzimas | |
dc.subject.decs | Asfixia | |
dc.subject.decs | Hipocampo | |
dc.subject.decs | Control social formal | |
dc.subject.decs | Enfermedades del sistema nervioso | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Animals, Newborn | |
dc.subject.mesh | Asphyxia Neonatorum | |
dc.subject.mesh | Corpus Striatum | |
dc.subject.mesh | Disease Models, Animal | |
dc.subject.mesh | Endocannabinoids | |
dc.subject.mesh | Lipoprotein Lipase | |
dc.subject.mesh | PPAR alpha | |
dc.subject.mesh | Phospholipase D | |
dc.subject.mesh | Rats | |
dc.subject.mesh | Rats, Sprague-Dawley | |
dc.subject.mesh | Receptor, Cannabinoid, CB1 | |
dc.subject.mesh | Signal Transduction | |
dc.title | Acylethanolamides and endocannabinoid signaling system in dorsal striatum of rats exposed to perinatal asphyxia. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 653 | |
dspace.entity.type | Publication |
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