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Interaction between adenosine A2A receptors and cannabinoid CB1 receptors at the hippocampus : consequences for memory and plasticity

datacite.subject.fosCiências Médicas::Medicina Básicapt_PT
dc.contributor.advisorSebastião, Ana Maria, 1958-
dc.contributor.authorMouro, Francisco Melo Albuquerque Saraiva, 1988-
dc.date.accessioned2018-08-23T10:57:41Z
dc.date.available2018-08-23T10:57:41Z
dc.date.issued2018
dc.date.submitted2017
dc.descriptionTese de doutoramento, Ciências Biomédicas (Neurociências), Universidade de Lisboa, Faculdade de Medicina, 2018pt_PT
dc.description.abstractAdenosine is an ubiquitous neuromodulator of the central nervous system (CNS) and through receptors of the A2A subtype (A2ARs) can influence both synaptic plasticity and neuronal death. Likewise, endocannabinoids are important neuromodulators that act at the CNS, being involved in several physiological processes. Activation of the cannabinoid receptor 1 (CB1Rs) is responsible for mediating the physiological actions of endocannabinoids and the psychoactive effects of Δ9-THC. Neuromodulators of the central nervous system show the ability to modify the activity of N-methyl-D-aspartate receptors (NMDARs), known to play a key role in both synaptic plasticity and neurodegeneration. Considering the prejudicial effects upon memory associated with cannabinoid consumption and that NMDARs can induce neurodegeneration and excitotoxicity, this work was designed to understand if adenosine A2AR activity could be pharmacologically manipulated to protect neurons and synapses from insults coming from cannabinoid exposure and NMDARs hyperfunction. The results show that an adenosine A2AR agonist could selectively increase synaptic NMDAR activity, known to be related with neuroprotection. Also, it is whereby demonstrated that the activation of CB1Rs is associated with long term potentiation (LTP) impairments and disruptions in recognition memory. Simultaneous administration of an A2ARs antagonist was able to partially restore LTP and to fully cancel impairments in recognition memory. Also, it was found that chronic cannabinoid exposure modified brain metabolic activity, resulting in patterns of abnormal functional connectivity within the limbic system. These results point to dysfunctionalities in a multiplitude of brain regions involved in recognition memory. This work highlights the ability of adenosine A2ARs to act as metamodulators of synaptic transmission in the CNS. The fact that these receptors are able of increasing and decreasing, respectively, the positive outcomes of synaptic NMDAR activity and the negative consequences of CB1Rs upon recognition memory, show the potential of A2AR as therapeutic targets to tackle neuronal imbalances in psychiatric and neurologic diseases.pt_PT
dc.identifier.tid101381220pt_PT
dc.identifier.urihttp://hdl.handle.net/10451/34560
dc.language.isoengpt_PT
dc.relationINTERACTION BETWEEN ADENOSINE A2A RECEPTORS AND CANNABINOID CB1 RECEPTORS AT THE HIPPOCAMPUS: CONSEQUENCES FOR PLASTICITY AND MEMORY
dc.subjectAdenosinapt_PT
dc.subjectReceptor A2A de adenosinapt_PT
dc.subjectCanabinóidespt_PT
dc.subjectReceptores de N-Metil-D-Aspartatopt_PT
dc.subjectMemóriapt_PT
dc.subjectPlasticidade neuronalpt_PT
dc.subjectTeses de doutoramento - 2018pt_PT
dc.titleInteraction between adenosine A2A receptors and cannabinoid CB1 receptors at the hippocampus : consequences for memory and plasticitypt_PT
dc.typedoctoral thesis
dspace.entity.typePublication
oaire.awardNumberSFRH/BD/89582/2012
oaire.awardTitleINTERACTION BETWEEN ADENOSINE A2A RECEPTORS AND CANNABINOID CB1 RECEPTORS AT THE HIPPOCAMPUS: CONSEQUENCES FOR PLASTICITY AND MEMORY
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F89582%2F2012/PT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsrestrictedAccesspt_PT
rcaap.typedoctoralThesispt_PT
relation.isProjectOfPublicationd53d8f49-8eed-4dc9-b642-ce9069f85346
relation.isProjectOfPublication.latestForDiscoveryd53d8f49-8eed-4dc9-b642-ce9069f85346
thesis.degree.nameDoutoramento em Ciências Biomédicaspt_PT

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