Modelling the role of glucocorticoid receptor as mediator of endocrine responses to environmental challenge

dc.contributor.authorJimeno, Blanca
dc.contributor.authorGallego Rubalcaba, Juan Vicente
dc.date.accessioned2025-03-31T12:01:22Z
dc.date.available2025-03-31T12:01:22Z
dc.date.issued2024
dc.descriptionB.J. was funded by the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 101027784. J.G.R. was funded by the Comunidad de Madrid's Research Talent Attraction Program for Senior Researchers (2022-T1/AMB-23753).
dc.description.abstractGlucocorticoid hormones (GCs) modulate acute ‘stress’ responses in vertebrates, exerting their actions across many physiological systems to help the organism face and overcome challenges. These actions take place via binding to the glucocorticoid receptor (GR), which determines not only the magnitude of the GC-mediated physiological response but also the negative feedback that downregulates GCs to restore homeostasis. Although GR function is assumed to determine GC regulation capacity, the associations between GR abundance and individuals' coping abilities remain cryptic. We developed a dynamic model fitted to empirical data to predict the effects of GR abundance on both plasma GC response patterns and the magnitude of GC-mediated physiological response. Individuals with higher GRs showed lower GC exposure, stronger physiological responses and greater capacity to adjust this response according to stressor intensity, which may be translated into more resilient and flexible GC phenotypes. Our results also show that among-individual variability in GR abundance challenges the detectability of the association between plasma GC measurements and physiological responses. Our approach provides mechanistic insights into the role of GRs in plasma GC measurements and function, which point at GR abundance fundamentally driving complex features of the GC regulation system in the face of environmental change.
dc.description.departmentDepto. de Biodiversidad, Ecología y Evolución
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipComunidad de Madrid
dc.description.statuspub
dc.identifier.citationJimeno Blanca and Rubalcaba Juan G. 2024Modelling the role of glucocorticoid receptor as mediator of endocrine responses to environmental challengePhil. Trans. R. Soc. B37920220501 http://doi.org/10.1098/rstb.2022.0501
dc.identifier.doi10.1098/rstb.2022.0501
dc.identifier.essn1471-2970
dc.identifier.issn0962-8436
dc.identifier.officialurlhttps://doi.org/10.1098/rstb.2022.0501
dc.identifier.relatedurlhttps://royalsocietypublishing.org/doi/10.1098/rstb.2022.0501
dc.identifier.urihttps://hdl.handle.net/20.500.14352/119057
dc.issue.number1898
dc.journal.titlePhilosophical Transactions of the Royal Society B: Biological Sciences
dc.language.isoeng
dc.publisherThe Royal Society Publishing
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/101027784/EU
dc.relation.projectIDS2022/AMB-23753
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu577.17
dc.subject.cdu577.2
dc.subject.cdu591.147
dc.subject.cdu574
dc.subject.keywordStress response
dc.subject.keywordEndocrine flexibility
dc.subject.keywordStress resilience
dc.subject.keywordDynamic model
dc.subject.keywordGlucocorticoid
dc.subject.keywordHypothalamic–pituitary–adrenal (HPA) axis
dc.subject.ucmBioquímica (Biología)
dc.subject.ucmBiología molecular (Biología)
dc.subject.ucmFisiología animal (Biología)
dc.subject.ucmEcología (Biología)
dc.subject.ucmEndocrinología
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2302.15 Hormonas
dc.subject.unesco2401.13 Fisiología Animal
dc.subject.unesco2401.06 Ecología Animal
dc.subject.unesco2415 Biología Molecular
dc.titleModelling the role of glucocorticoid receptor as mediator of endocrine responses to environmental challenge
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number379
dspace.entity.typePublication
relation.isAuthorOfPublicationdd93fbb4-852a-4091-aa03-9f80b247549b
relation.isAuthorOfPublication.latestForDiscoverydd93fbb4-852a-4091-aa03-9f80b247549b

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