Metabotropic glutamate 5 receptor in the infralimbic cortex contributes to descending pain facilitation in healthy and arthritic animals

dc.contributor.authorPereira, Ana Carla Davidpor
dc.contributor.authorPuga, Sónia Andreia Silvapor
dc.contributor.authorGonçalves, S.por
dc.contributor.authorAmorim, Diana Alexandra Silvapor
dc.contributor.authorSilva, Carmen L. O.por
dc.contributor.authorPertovaara, A.por
dc.contributor.authorAlmeida, Armandopor
dc.contributor.authorPinto-Ribeiro, Filipapor
dc.date.accessioned2017-03-09T11:26:58Z
dc.date.available2017-03-09T11:26:58Z
dc.date.issued2016-01
dc.date.updated2017-02-14T11:34:03Z
dc.description.abstractThe involvement of the prefrontal cortex in pain processing has been recently addressed. We studied the role of the infralimbic cortex (IL) and group I metabotropic glutamate receptors (mGluRs) in descending modulation of nociception in control and monoarthritic (ARTH) conditions. Nociception was assessed using heat-induced paw withdrawal while drugs were microinjected in the IL of rats. Local anesthesia of the IL or the adjacent prelimbic cortex (PL) facilitated nociception, indicating that IL and PL are tonically promoting spinal antinociception. Phasic activation with glutamate (GLU) revealed opposing roles of the PL and IL; GLU in the PL had a fast antinociceptive action, while in the IL it had a slow onset pronociceptive action. IL administration of a local anesthetic or GLU produced identical results in ARTH and control animals. An mGluR5 agonist in the IL induced a pronociceptive effect in both groups, while mGluR5 antagonists had no effect in controls but induced antinociception in ARTH rats. Activation of the IL mGluR1 (through co-administration of mGluR1/5 agonist and mGluR5 antagonist) did not alter nociception in controls but induced antinociception in ARTH animals. IL administration of an mGluR1 antagonist failed to alter nociception in either experimental group. Finally, mGluR5 but not mGluR1 antagonists blocked the pronociceptive action of GLU in both groups. The results indicate that IL contributes to descending modulation of nociception. mGluR5 in the IL enhance nociception in healthy control and monoarthritic animals, an effect that is tonic in ARTH. Moreover, activation of IL mGluR1s attenuates nociception following the development of monoarthritis.por
dc.description.sponsorshipPortuguese Science Foundation (FCT) Project PTDC/SAU-NEU/108557/2008, FEDER-COMPETE, by the Academy of Finland and the Sigrid Juselius Foundation, Helsinki, Finland and co‐financed by the Portuguese North Regional Operational Program (ON.2 – O Novo Norte) under the National Strategic Reference Framework (QREN), through the European Regional Development Fund (FEDER).por
dc.distributioninternationalpor
dc.identifier.citationDavid-Pereira, A., Puga, S., Goncalves, S., Amorim, D., Silva, C., et. al.(2016). Metabotropic glutamate 5 receptor in the infralimbic cortex contributes to descending pain facilitation in healthy and arthritic animals. Neuroscience, 312, 108-119por
dc.identifier.doi10.1016/j.neuroscience.2015.10.060por
dc.identifier.issn0306-4522por
dc.identifier.pmid26548413por
dc.identifier.urihttps://hdl.handle.net/1822/44943
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F90374%2F2012/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F71219%2F2010/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/108557/PTpor
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S0306452215009884por
dc.rightsopenAccesspor
dc.subjectInfralimbic cortexpor
dc.subjectMetabotropic glutamate receptor 5por
dc.subjectExperimental monoarthritispor
dc.subjectPronociceptionpor
dc.subject.fosCiências Médicas::Medicina Básicapor
dc.subject.wosScience & Technologypor
dc.titleMetabotropic glutamate 5 receptor in the infralimbic cortex contributes to descending pain facilitation in healthy and arthritic animalspor
dc.typearticle
dspace.entity.typePublicationen
oaire.citationEndPage119por
oaire.citationStartPage108por
oaire.citationTitleNeurosciencepor
oaire.citationVolume312por
sdum.journalNeurosciencepor
sdum.publicationstatusinfo:eu-repo/semantics/publishedVersionpor

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