Modelling the role of glucocorticoid receptor as mediator of endocrine responses to environmental challenge
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2024
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The Royal Society Publishing
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Jimeno 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
Abstract
Glucocorticoid 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.
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B.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).












