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Publication : Peripheral mechanisms contributing to the glucocorticoid hypersensitivity in proopiomelanocortin null mice treated with corticosterone.

First Author  Michailidou Z Year  2007
Journal  J Endocrinol Volume  194
Issue  1 Pages  161-70
PubMed ID  17592030 Mgi Jnum  J:122402
Mgi Id  MGI:3714236 Doi  10.1677/JOE-07-0090
Citation  Michailidou Z, et al. (2007) Peripheral mechanisms contributing to the glucocorticoid hypersensitivity in proopiomelanocortin null mice treated with corticosterone. J Endocrinol 194(1):161-170
abstractText  Proopiomelanocortin (POMC) deficiency causes severe obesity through hyperphagia of hypothalamic origin. However, low glucocorticoid levels caused by adrenal insufficiency mitigate against insulin resistance, hyperphagia and fat accretion in Pomc(-/-)mice. Upon exogenous glucocorticoid replacement, corticosterone-supplemented (CORT) Pomc(-/-) mice show exaggerated responses, including excessive fat accumulation, hyperleptinaemia and insulin resistance. To investigate the peripheral mechanisms underlying this glucocorticoid hypersensitivity, we examined the expression levels of key determinants and targets of glucocorticoid action in adipose tissue and liver. Despite lower basal expression of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1), which generates active glucocorticoids within cells, CORT-mediated induction of 11beta-HSD1 mRNA levels was more pronounced in adipose tissues of Pomc(-/-)mice. Similarly, CORT treatment increased lipoprotein lipase mRNA levels in all fat depots in Pomc(-/-) mice, consistent with exaggerated fat accumulation. Glucocorticoid receptor (GR) mRNA levels were selectively elevated in liver and retroperitoneal fat of Pomc(-/-) mice but were corrected by CORT in the latter depot. In liver, CORT increased phosphoenolpyruvate carboxykinase mRNA levels specifically in Pomc(-/-) mice, consistent with their insulin-resistant phenotype. Furthermore, CORT induced hypertension in Pomc(-/-)mice, independently of adipose or liver renin-angiotensin system activation. These data suggest that CORT-inducible 11beta-HSD1 expression in fat contributes to the adverse cardiometabolic effects of CORT in POMC deficiency, whereas higher GR levels may be more important in liver.
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