Prednisolone induces the Wnt signalling pathway in 3T3-L1 adipocytes

Autor: Wim H. A. Dokter, Bruno Guigas, Jacob de Vlieg, Wynand Alkema, Margot M. Linssen, Wilco W. M. Fleuren, D. Margriet Ouwens, Erik J M Toonen, Gerard C.M. van der Zon
Přispěvatelé: Data Sciences for Life Science & Health
Rok vydání: 2013
Předmět:
Physiology
medicine.medical_treatment
Gene Expression
Adipose tissue
transcriptome/drug effects
prednisolone/adverse effects
adipocytes/drug effects
0302 clinical medicine
insulin resistance
Adipocytes
Insulin
Wnt Signaling Pathway
0303 health sciences
glucocorticoids
adipokines/genetics
insulin/pharmacology
Health aging / healthy living Pathogenesis and modulation of inflammation [IGMD 5]
Wnt signaling pathway
signal transduction/drug effects
General Medicine
3. Good health
Cell biology
immunity/drug effects
3t3-l1 cells
Signal transduction
Signal Transduction
Chemical and physical biology [NCMLS 7]
medicine.medical_specialty
mice
Prednisolone
Adipokine
030209 endocrinology & metabolism
Deoxyglucose
Biology
glucocorticoids/adverse effects
03 medical and health sciences
Insulin resistance
Adipokines
Gene profiling
Physiology (medical)
Internal medicine
medicine
Animals
Secretion
deoxyglucose/metabolism
030304 developmental biology
metabolic dysfunction
biochemie
gene expression/drug effects
Immunity
3T3-L1
Original Articles
medicine.disease
Endocrinology
Tissue Array Analysis
Research Programm of Institute for Molecules and Materials
Transcriptome
Zdroj: Archives of Physiology and Biochemistry, 119, 52-64
Archives of Physiology and Biochemistry, 119(2), 52-64
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry, 119(2), 52-64. Swets & Zeitlinger
Archives of Physiology and Biochemistry, 119, 2, pp. 52-64
ISSN: 1381-3455
Popis: Contains fulltext : 117166.pdf (Publisher’s version ) (Open Access) Synthetic glucocorticoids are potent anti-inflammatory drugs but show dose-dependent metabolic side effects such as the development of insulin resistance and obesity. The precise mechanisms involved in these glucocorticoid-induced side effects, and especially the participation of adipose tissue in this are not completely understood. We used a combination of transcriptomics, antibody arrays and bioinformatics approaches to characterize prednisolone-induced alterations in gene expression and adipokine secretion, which could underlie metabolic dysfunction in 3T3-L1 adipocytes. Several pathways, including cytokine signalling, Akt signalling, and Wnt signalling were found to be regulated at multiple levels, showing that these processes are targeted by prednisolone. These results suggest that mechanisms by which prednisolone induce insulin resistance include dysregulation of wnt signalling and immune response processes. These pathways may provide interesting targets for the development of improved glucocorticoids.
Databáze: OpenAIRE