Literature DB >> 17624658

Glucocorticoids, metabolism and metabolic diseases.

Alexandros Vegiopoulos1, Stephan Herzig.   

Abstract

Since the discovery of the beneficial effects of adrenocortical extracts for treating adrenal insufficiency more than 80 years ago, glucocorticoids (GC) and their cognate, intracellular receptor, the glucocorticoid receptor (GR) have been characterized as critical components of the delicate hormonal control system that determines energy homeostasis in mammals. Whereas physiological levels of GCs are required for proper metabolic control, excessive GC action has been tied to a variety of pandemic metabolic diseases, such as type II diabetes and obesity. Highlighted by its importance for human health, the investigation of molecular mechanisms of GC/GR action has become a major focus in biomedical research. In particular, the understanding of tissue-specific functions of the GC-GR pathway has been proven to be of substantial value for the identification of novel therapeutic options in the treatment of severe metabolic disorders. Therefore, this review focuses on the role of the GC-GR axis for metabolic homeostasis and dysregulation, emphasizing tissue-specific functions of GCs in the control of energy metabolism.

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Year:  2007        PMID: 17624658     DOI: 10.1016/j.mce.2007.05.015

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  152 in total

1.  Activation of the farnesoid X receptor induces hepatic expression and secretion of fibroblast growth factor 21.

Authors:  Holly A Cyphert; Xuemei Ge; Alison B Kohan; Lisa M Salati; Yanqiao Zhang; F Bradley Hillgartner
Journal:  J Biol Chem       Date:  2012-06-01       Impact factor: 5.157

Review 2.  The role of CREB-H transcription factor in triglyceride metabolism.

Authors:  Ann-Hwee Lee
Journal:  Curr Opin Lipidol       Date:  2012-04       Impact factor: 4.776

3.  Loss of the glucocorticoid receptor in zebrafish improves muscle glucose availability and increases growth.

Authors:  Erin Faught; Mathilakath M Vijayan
Journal:  Am J Physiol Endocrinol Metab       Date:  2019-04-02       Impact factor: 4.310

4.  Mechanistic Multi-Tissue Modeling of Glucocorticoid-Induced Leucine Zipper Regulation: Integrating Circadian Gene Expression with Receptor-Mediated Corticosteroid Pharmacodynamics.

Authors:  Vivaswath S Ayyar; Debra C DuBois; Richard R Almon; William J Jusko
Journal:  J Pharmacol Exp Ther       Date:  2017-07-20       Impact factor: 4.030

5.  Glucocorticoid receptor β stimulates Akt1 growth pathway by attenuation of PTEN.

Authors:  Lance A Stechschulte; Leah Wuescher; Joseph S Marino; Jennifer W Hill; Charis Eng; Terry D Hinds
Journal:  J Biol Chem       Date:  2014-05-09       Impact factor: 5.157

6.  Glucocorticoid Induces Hepatic Steatosis by Inhibiting Activating Transcription Factor 3 (ATF3)/S100A9 Protein Signaling in Granulocytic Myeloid-derived Suppressor Cells.

Authors:  Yu-Feng Liu; Jian-Yang Wei; Mao-Hua Shi; Hua Jiang; Jie Zhou
Journal:  J Biol Chem       Date:  2016-08-29       Impact factor: 5.157

Review 7.  COUP-TFII revisited: Its role in metabolic gene regulation.

Authors:  Usman M Ashraf; Edwin R Sanchez; Sivarajan Kumarasamy
Journal:  Steroids       Date:  2018-11-24       Impact factor: 2.668

8.  Adult consequences of post-weaning high fat feeding on the limbic-HPA axis of female rats.

Authors:  George Boukouvalas; Kyriaki Gerozissis; Efthimia Kitraki
Journal:  Cell Mol Neurobiol       Date:  2009-11-10       Impact factor: 5.046

9.  FKBP51 controls cellular adipogenesis through p38 kinase-mediated phosphorylation of GRα and PPARγ.

Authors:  Lance A Stechschulte; Terry D Hinds; Saja S Khuder; Weinian Shou; Sonia M Najjar; Edwin R Sanchez
Journal:  Mol Endocrinol       Date:  2014-06-16

10.  FKBP51 reciprocally regulates GRα and PPARγ activation via the Akt-p38 pathway.

Authors:  Lance A Stechschulte; Terry D Hinds; Simona S Ghanem; Weinian Shou; Sonia M Najjar; Edwin R Sanchez
Journal:  Mol Endocrinol       Date:  2014-06-16
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