Mifepristone for treatment of metabolic syndrome: beyond cushing’s syndrome
Author
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Díaz Castro, Francisco
Author
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Monsalves Álvarez, Matías
Author
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Rojo, Leonel E.
Author
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Campo, Andrea del
Author
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Troncoso, Rodrigo
Admission date
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2020-06-16T22:23:17Z
Available date
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2020-06-16T22:23:17Z
Publication date
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2020
Cita de ítem
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Front Pharmacol .(2020);11:429
es_ES
Identifier
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10.3389/fphar.2020.00429
Identifier
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https://repositorio.uchile.cl/handle/2250/175524
Abstract
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A growing body of research indicates that cortisol, the glucocorticoid product of the activation of the hypothalamic-pituitary-adrenal axis, plays a role in the pathophysiology of metabolic syndrome. In this regard, chronic exposure to cortisol is associated with risk factors related to metabolic syndrome like weight gain, type 2 diabetes, hypertension, among others. Mifepristone is the only FDA-approved drug with antiglucocorticoids properties for improved the glycemic control in patients with type 2 patients secondary to endogenous Cushing's syndrome. Mifepristone also have been shown positive effects in rodents models of diabetes and patients with obesity due to antipsychotic treatment. However, the underlying molecular mechanisms are not fully understood. In this perspective, we summarized the literature regarding the beneficial effects of mifepristone in metabolic syndrome from animal studies to clinical research. Also, we propose a potential mechanism for the beneficial effects in insulin sensitivity which involved the regulation of mitochondrial function in muscle cells.
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Patrocinador
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Enlace FONDECYT-VID: EN29/18
Comisión Nacional de Investigación Cientifica y Tecnológica (CONICYT) CONICYT FONDECYT 1191078 11190756
FONDAP 15130011