Title of article
Brain-Derived Neurotrophic Factor, Food Intake Regulation, and Obesity
Author/Authors
Rosas-Vargas، نويسنده , , Haydeé and Martيnez-Ezquerro، نويسنده , , José Darيo and Bienvenu، نويسنده , , Thierry، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2011
Pages
13
From page
482
To page
494
Abstract
Brain-derived neurotrophic factor (BDNF) is a neurotrophin that plays a fundamental role in development and plasticity of the central nervous system (CNS). It is currently recognized as a major participant in the regulation of food intake. Multiple studies have shown that different regulators of appetite such as leptin, insulin and pancreatic polypeptide (PP) potentially exert anorexigenic effects through BDNF. Low circulating levels of BDNF are associated with a higher risk of eating disorders such as anorexia nervosa (AN) and bulimia nervosa (BN). Strict food restriction reduces BDNF and may trigger binge-eating episodes and weight gain. The existence of mutations that cause haploinsufficiency of BDNF as well as some genetic variants, notably the BDNF p.Val66Met polymorphism, are also associated with the development of obese phenotypes and hyperphagia. However, association of the Met allele with AN and BN, which have different phenotypic characteristics, shows clearly the existence of other relevant factors that regulate eating behavior. This may, in part, be explained by the epigenetic regulation of BDNF through mechanisms like DNA methylation and histone acetylation. Environmental factors, primarily during early development, are crucial to the establishment of these stable but reversible changes that alter the transcriptional expression and are transgenerationally heritable, with potential concomitant effects on the development of eating disorders and body weight control.
Keywords
eating behavior , Obesity , Energy homeostasis , Brain-derived neurotrophic factor , neurotrophin
Journal title
Archives of Medical Research
Serial Year
2011
Journal title
Archives of Medical Research
Record number
1797598
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