Back to Search
Start Over
Peroxisome proliferator-activated receptor-γ: Master regulator of adipogenesis and obesity
- Source :
- Scopus-Elsevier
-
Abstract
- Obesity, which is a key risk for the development of hyperglycemia, hypertension, hyperlipidemia and insulin resistance and is totally referred to as the metabolic disorders, has aroused people's great attention because of its alarming increase rate around the world. It is widely known that the occurrence of obesity can be attributed to both environmental and genetic factors. Peroxisome proliferators-activated receptor (PPAR), a member of ligand-dependent receptor, is one of the important genetic factors. PPAR includes three isoforms: PPAR-α, PPAR- β and PPAR- γ, all of which are exerting critical influences on the maintenance of the metabolism of saccharides, lipids and proteins. PPAR-γ is of great importance in the regulation of adipogenesis; in addition, it is essential in the prevention of adiposis and the treatment of 2-diabetes mellitus. In this review, we focus on giving a brief introduction about PPAR family, the indispensible function of PPAR-γ in adipogenesis and the inseparable relationship between PPAR-γ and obesity, deriving from the understanding of how these receptors activated will provide windows of opportunities for the treatment of obesity and associated metabolism syndromes.
- Subjects :
- 0301 basic medicine
medicine.medical_specialty
Medicine (miscellaneous)
Peroxisome proliferator-activated receptor
Biology
Ligands
PPAR agonist
03 medical and health sciences
Insulin resistance
Internal medicine
Diabetes mellitus
Hyperlipidemia
medicine
Humans
Obesity
Receptor
chemistry.chemical_classification
Adipogenesis
General Medicine
Peroxisome
medicine.disease
Lipid Metabolism
PPAR gamma
030104 developmental biology
Endocrinology
chemistry
Diabetes Mellitus, Type 2
Carbohydrate Metabolism
lipids (amino acids, peptides, and proteins)
Thiazolidinediones
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Scopus-Elsevier
- Accession number :
- edsair.doi.dedup.....2d95b025bfbc1174f914eb81771d75ff