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dc.contributor.authorPalumbo, María Lauraes
dc.contributor.authorProchnik, Andréses
dc.contributor.authorWald, Miriam Ruthes
dc.contributor.authorGenaro, Ana Maríaes
dc.date.accessioned2020-05-21T22:16:22Z-
dc.date.available2020-05-21T22:16:22Z-
dc.date.issued2020-
dc.identifier.citationPalumbo, M. L., et al. Chronic stress and glucocorticoid receptor resistance in asthma [en línea]. Postprint del artículo publicado en Clinical Therapeutics. 2020. doi: 10.1016/j.clinthera.2020.03.002. Disponible en: https://repositorio.uca.edu.ar/handle/123456789/10052es
dc.identifier.issn0149-2918 (online)-
dc.identifier.urihttps://repositorio.uca.edu.ar/handle/123456789/10052-
dc.description.abstractAbstract: Purpose: Chronic and persistent exposure to negative stress can lead to adverse consequences on health. Particularly, psychosocial factors were found to increase the risk and outcome of respiratory diseases like asthma. Glucocorticoids (GCs) are the most efficient anti-inflammatory therapy for asthma. However, a significant proportion of patients don’t respond adequately to GC administration. GC sensitivity is modulated by genetic and acquired disease-related factors. Additionally, it was proposed that endogenous corticosteroids may limit certain actions of synthetic GCs, contributing to insensitivity. Psychological and physiological stresses activate the hypothalamic-pituitary-adrenal axis, increasing cortisol levels. Here, we review the mechanism involved in altered GC sensitivity in asthmatic patients under stressful situations. Strategies for modulation GC sensitivity and improving GC therapy are discussed. Methods: PubMed was searched for publications on psychological chronic stress and asthma, GC resistance in asthma, biological mechanisms for GC resistance, and drugs for steroid-resistant asthma, including highly potent GCs. Findings: GC resistance in patients with severe disease remains a major clinical problem. In asthma, experimental and clinical evidence suggests that chronic stress induces inflammatory changes, contributing to a worse GC response. GC resistant patients can be treated with other broad-spectrum anti-inflammatory drugs, but these generally have major side effects. Different mechanisms of GC resistance have been described and might be useful for developing new therapeutic strategies against it. Novel drugs, such as highly potent GCs, phosphoinositide 3-kinase-delta inhibitors that reestablish histone deacetylase-2 function, decrease of GC receptor phosphorylation by p38 mitogenactivated protein kinase inhibitors, or phosphatase activators, are currently in clinical development and might be combined with GC therapy in the future. Furthermore, microRNAs (small noncoding RNA molecules) operate as posttranscriptional regulators, providing another level of control of GC receptor levels. Empirical results allow postulating that the detection and study of microRNAs might be a promising approach to better characterize and treat asthmatic patients. Implications: Many molecular and cellular pathobiological mechanisms are responsible of GC resistance. Therefore detecting specific biomarkers to help identify patients who would benefit from new therapies is crucial. Stress consitutes a negative aspect of current lifestyles that increase asthma morbidity and mortality. Adequate stress management could be an important and positive intervention. Key words: asthma, chronic stress, glucocorticoid resistance, pharmacologic strategies.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rightsAcceso abierto. 12 meses de embargo*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.sourceClinical Therapeutics. 2020es
dc.subjectASMAes
dc.subjectCORTICOIDESes
dc.subjectTRATAMIENTO MEDICOes
dc.subjectTRATAMIENTO FARMACOLOGICOes
dc.subjectESTRESes
dc.subjectFACTORES PSICOLOGICOSes
dc.titleChronic stress and glucocorticoid receptor resistance in asthmaes
dc.typeArtículoes
dc.identifier.doi10.1016/j.clinthera.2020.03.002-
uca.disciplinaMEDICINAes
uca.issnrd1es
uca.affiliationFil: Palumbo, María Laura. Centro de Investigaciones y Transferencia del Noroeste de la Provincia de Buenos Aires; Argentinaes
uca.affiliationFil: Palumbo, María Laura. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes
uca.affiliationFil: Prochnik, Andrés. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Biomedicas; Argentinaes
uca.affiliationFil: Prochnik, Andrés. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes
uca.affiliationFil: Wald, Miriam Ruth. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Biomedicas; Argentinaes
uca.affiliationFil: Wald, Miriam Rut. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes
uca.affiliationFil: Genaro, Ana María. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Farmacología; Argentinaes
uca.versionacceptedVersiones
item.languageiso639-1en-
item.grantfulltextopen-
item.fulltextWith Fulltext-
crisitem.author.deptInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.deptLaboratorio de Psiconeuroendocrinoinmunología-
crisitem.author.deptConsejo Nacional de Investigaciones Científicas y Técnicas-
crisitem.author.deptFacultad de Ciencias Médicas-
crisitem.author.deptInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.deptLaboratorio de Psiconeuroendocrinoinmunología-
crisitem.author.deptConsejo Nacional de Investigaciones Científicas y Técnicas-
crisitem.author.deptFacultad de Ciencias Médicas-
crisitem.author.deptInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.deptLaboratorio de Psiconeuroendocrinoinmunología-
crisitem.author.deptPontificia Universidad Católica Argentina-
crisitem.author.deptFacultad de Ciencias Médicas-
crisitem.author.deptFacultad de Ciencias Médicas-
crisitem.author.deptInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.deptLaboratorio de Psiconeuroendocrinoinmunología-
crisitem.author.orcid0000-0002-8748-2027-
crisitem.author.orcid0000-0001-9216-2880-
crisitem.author.orcid0000-0003-0027-3503-
crisitem.author.parentorgFacultad de Ciencias Médicas-
crisitem.author.parentorgInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.parentorgPontificia Universidad Católica Argentina-
crisitem.author.parentorgFacultad de Ciencias Médicas-
crisitem.author.parentorgInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.parentorgPontificia Universidad Católica Argentina-
crisitem.author.parentorgFacultad de Ciencias Médicas-
crisitem.author.parentorgInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.parentorgPontificia Universidad Católica Argentina-
crisitem.author.parentorgPontificia Universidad Católica Argentina-
crisitem.author.parentorgFacultad de Ciencias Médicas-
crisitem.author.parentorgInstituto de Investigaciones Biomédicas - BIOMED-
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