Abstract
Individuals who live in industrialized countries often eat a calorie-rich diet and perform little physical activity. These habits are thought to be critical contributors to the rapidly rising incidence of obesity, a condition that affects hundreds of millions of people worldwide. High-calorie intake alters metabolic-sensing pathways in central nervous system neurons, and these changes have pathogenic roles in the development of obesity. This review aims to summarize our current knowledge about the neuronal populations (the central melanocortin system in particular) and transcriptional regulators, including STAT3 and FOXO1, that are involved in the maintenance of normal body weight. We describe the interactions between these transcriptional factors and their target genes, which encode the main appetite-regulating neuropeptides (agouti-related peptide and α-melanocyte-stimulating hormone). We discuss the transcriptional co-activator PGC-1-α and the supposed metabolic-sensor protein SIRT1, and their potential roles as targets for novel antiobesity medications.
Original language | English (US) |
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Pages (from-to) | 160-166 |
Number of pages | 7 |
Journal | Nature Clinical Practice Endocrinology and Metabolism |
Volume | 5 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2009 |
Keywords
- Body-weight homeostasis
- Feeding
- Melanocortin system
- Obesity
- Transcription factors
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
- Endocrinology