Título
Ketoconazole, an Antifungal Agent, Protects Against Adiposity Induced by a Cafeteria DietVersión
PreprintTipo de documento
ArtículoIdioma
InglésAcceso
Acceso abiertoVersión de la editorial
https://doi.org/10.1055/s-2004-825729Publicado en
Hormone and metabolic research n.7, vol. 36, n.art. 485Primera página
485Última página
491Palabras clave
High fat diet
glucocorticoids
lipolysis
adipocytes ... [+]
glucocorticoids
lipolysis
adipocytes ... [+]
High fat diet
glucocorticoids
lipolysis
adipocytes
obesity/overweight
rat [-]
glucocorticoids
lipolysis
adipocytes
obesity/overweight
rat [-]
Resumen
Ketoconazole, an anti-glucocorticoid agent, is widely used in humans as an antifungal agent. It inhibits ergosterol synthesis and reduces cortisol levels in the treatment of Cushing’s Syndrome. The ai ... [+]
Ketoconazole, an anti-glucocorticoid agent, is widely used in humans as an antifungal agent. It inhibits ergosterol synthesis and reduces cortisol levels in the treatment of Cushing’s Syndrome. The aim of this work was to study the drug’s preventive potential against adiposity induced by a high-fat cafeteria diet in rats. Female Wistar rats were fed on standard pelleted diet or cafeteria diet during 42 days in the presence or absence of an oral treatment with ketoconazole (24 mg/kg of body weight). The cafeteria diet increased energy intake and body weight. In addition, this high-fat diet increased body-fat weight and adipose tissue depots analyzed. Interestingly, ketoconazole was able to protect against increased total body fat and adipose depot enlargement induced after cafeteria-diet feeding. Moreover, ex vivo isoproterenol-induced lipolysis was reduced in adipocytes from cafeteria-fed animals; this decrease was reverted by treatment with ketoconazole. Thus, ketoconazole was able to protect against adiposity induced by a cafeteria diet, revealing an interaction between fat intake and glucocorticoids on adipose deposition. [-]



















