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Spinal Involvement of TRPV1 and PI3K/AKT/mTOR Pathway During Chronic Postoperative Pain in Mice

dc.contributor.authorSantos, Gabriela Xavier
dc.contributor.authordos Anjos-Garcia, Tayllon [UNESP]
dc.contributor.authorVieira, Ana Carolina de Jesus
dc.contributor.authorGaldino, Giovane
dc.contributor.institutionFederal University of Alfenas
dc.contributor.institutionPadre Gervásio National Institute of Higher Education and Postgraduate Studies
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:57:34Z
dc.date.issued2025-01-01
dc.description.abstractBackground: Chronic postoperative pain (CPOP) is among the main consequences of surgical procedures, directly affecting the quality of life. Although many strategies have been used to treat this symptom, they are often ineffective. Thus, studies investigating CPOP-associated mechanisms may help to develop more effective treatment strategies. Therefore, the present study investigated the spinal participation of the transient potential receptor vanilloid type 1 (TRPV1) and PI3K/AKT/mTOR pathway activation during CPOP. Methods: In this study C57BL/6 male mice were used, and CPOP was induced by muscle retraction and incision. The nociceptive threshold was measured by the von Frey filament test. For pharmacological evaluation, TRPV1 and PI3K/AKT/mTOR inhibitors were administered intrathecally. TRPV1 and PI3K/AKT/mTOR protein levels were evaluated by Western blotting. Results: The results showed that CPOP increased TRPV1 and mTOR protein levels, and pretreatment with the specific inhibitors alleviated CPOP. In addition, pretreatment with the TRPV1 antagonist SB-366791 attenuated mTOR protein levels. Conclusions: The results suggest that TRPV1 and the PI3K/AKT/mTOR pathway are involved in CPOP at the spinal level, and TRPV1 may activate mTOR during this process.en
dc.description.affiliationCenter for Experimental Biology Laboratory of Neuroimmunobiology of Pain Federal University of Alfenas, MG
dc.description.affiliationInapós College Padre Gervásio National Institute of Higher Education and Postgraduate Studies, MG
dc.description.affiliationDepartment of Animal Morphology and Physiology of the Faculty of Agricultural and Veterinary Sciences of São Paulo State University, SP
dc.description.affiliationUnespDepartment of Animal Morphology and Physiology of the Faculty of Agricultural and Veterinary Sciences of São Paulo State University, SP
dc.identifierhttp://dx.doi.org/10.3390/brainsci15010053
dc.identifier.citationBrain Sciences, v. 15, n. 1, 2025.
dc.identifier.dimensionspub.1184274305
dc.identifier.doi10.3390/brainsci15010053
dc.identifier.issn2076-3425
dc.identifier.orcid0000-0002-1898-1973
dc.identifier.orcid0000-0003-0935-8861
dc.identifier.pmcidPMC11763465
dc.identifier.pmid39851421
dc.identifier.scopus2-s2.0-85215966775
dc.identifier.urihttps://hdl.handle.net/11449/301233
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofBrain Sciences
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceScopus
dc.sourceDimensions
dc.subjectchronic postoperative pain
dc.subjectmTOR
dc.subjectPI3K
dc.subjectTRPV1
dc.titleSpinal Involvement of TRPV1 and PI3K/AKT/mTOR Pathway During Chronic Postoperative Pain in Miceen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication3d807254-e442-45e5-a80b-0f6bf3a26e48
relation.isOrgUnitOfPublication.latestForDiscovery3d807254-e442-45e5-a80b-0f6bf3a26e48
unesp.author.orcid0000-0003-0935-8861[2]
unesp.author.orcid0000-0002-1898-1973[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Agrárias e Veterinárias, Jaboticabalpt

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