| Literature DB >> 28576418 |
Mariana Schroeder1, Mira Jakovcevski2, Tamar Polacheck1, Maya Lebow1, Yonat Drori1, Mareen Engel2, Shifra Ben-Dor3, Alon Chen4.
Abstract
Binge eating (BE) is a common aberrant form of eating behavior, characterized by overconsumption of food in a brief period of time. Recurrent episodes of BE constitute the BE disorder, which mostly affects females and is associated with early-life adversities. Here, we show that corticotropin releasing factor (CRF)-induced prenatal stress (PNS) in late gestation predisposes female offspring to BE-like behavior that coincides with hypomethylation of hypothalamic miR-1a and downstream dysregulation of the melanocortin system through Pax7/Pax3. Moreover, exposing the offspring to a methyl-balanced diet during adolescence prevents the dysregulation and predisposition from being triggered. We demonstrate that gestational programming, per se, will not lead to BE-like behavior, but pre-existing alterations due to prenatal programming are revealed only when challenged during adolescence. We provide experimental evidence for long-term epigenetic abnormalities stemming from PNS in predisposing female offspring to BE disorder as well as a potential non-invasive prevention strategy.Entities:
Keywords: CRF; binge eating; developmental origin of disease hypothesis; developmental programming; dietary manipulations; early-life adversities; eating behavior; eating disorder; methyl balanced diet; prenatal stress
Mesh:
Year: 2017 PMID: 28576418 DOI: 10.1016/j.cmet.2017.05.001
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287