Abstract The glucocorticoid receptor (GR) and peroxisome proliferator-activated receptors (PPARs) play important roles in both physiological and pathological conditions such as cell differentiation, lipolysis, control of glucose metabolism, immunity, and inflammation. In fact, recent studies suggest that the thiazolidinedione (TZD) class of PPAR-gamma ligands, like glucocorticoids, may also be clinically beneficial in several inflammatory diseases, even if the molecular mechanisms responsible for these activities have not yet been clarified. In this study, by using a murine model of inflammation, the carrageenin-induced paw edema in mouse, we show that the anti-inflammatory activity exhibited by the PPAR-gamma agonists rosiglitazone and ciglitazone is reversed by the GR antagonist RU486 (17 beta-hydroxy-11 beta-[4-dimethylamino phenyl]-17 alpha-[1-propynyl]estra-4,9-dien-3-one). Moreover, by using a conditional GR null cell line, we demonstrate, for the first time to our knowledge, that one of the possible mechanisms explaining the anti-inflammatory activity of TZDs is their ability to activate GR nuclear translocation. In addition, by using J774 cell line lacking PPAR-gamma, we demonstrate that PPAR-gamma expression could not be essential for TZD-mediated GR nuclear translocation, thus explaining, at least in part, the molecular mechanism underlying their anti-inflammatory activity.

Mechanism of the anti-inflammatory effect of thiazolidindiones. Relationship with the glucocorticoid pathway / Ialenti, Armando; Grassia, Gianluca; DI MEGLIO, P; Maffia, Pasquale; DI ROSA, M; Ianaro, Angela. - In: MOLECULAR PHARMACOLOGY. - ISSN 0026-895X. - STAMPA. - 67:(2005), pp. 1620-1628.

Mechanism of the anti-inflammatory effect of thiazolidindiones. Relationship with the glucocorticoid pathway.

IALENTI, ARMANDO;GRASSIA, GIANLUCA;MAFFIA, PASQUALE;IANARO, ANGELA
2005

Abstract

Abstract The glucocorticoid receptor (GR) and peroxisome proliferator-activated receptors (PPARs) play important roles in both physiological and pathological conditions such as cell differentiation, lipolysis, control of glucose metabolism, immunity, and inflammation. In fact, recent studies suggest that the thiazolidinedione (TZD) class of PPAR-gamma ligands, like glucocorticoids, may also be clinically beneficial in several inflammatory diseases, even if the molecular mechanisms responsible for these activities have not yet been clarified. In this study, by using a murine model of inflammation, the carrageenin-induced paw edema in mouse, we show that the anti-inflammatory activity exhibited by the PPAR-gamma agonists rosiglitazone and ciglitazone is reversed by the GR antagonist RU486 (17 beta-hydroxy-11 beta-[4-dimethylamino phenyl]-17 alpha-[1-propynyl]estra-4,9-dien-3-one). Moreover, by using a conditional GR null cell line, we demonstrate, for the first time to our knowledge, that one of the possible mechanisms explaining the anti-inflammatory activity of TZDs is their ability to activate GR nuclear translocation. In addition, by using J774 cell line lacking PPAR-gamma, we demonstrate that PPAR-gamma expression could not be essential for TZD-mediated GR nuclear translocation, thus explaining, at least in part, the molecular mechanism underlying their anti-inflammatory activity.
2005
Mechanism of the anti-inflammatory effect of thiazolidindiones. Relationship with the glucocorticoid pathway / Ialenti, Armando; Grassia, Gianluca; DI MEGLIO, P; Maffia, Pasquale; DI ROSA, M; Ianaro, Angela. - In: MOLECULAR PHARMACOLOGY. - ISSN 0026-895X. - STAMPA. - 67:(2005), pp. 1620-1628.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/202317
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