Evidence suggests that binge eating may be caused by a unique interaction between dieting and stress. We developed a binge-eating model in which female rats with a history of intermittent food restriction show binge-like palatable food consumption after 15 min exposure to the sight of the palatable food (frustration stress). Aim of the present study was to investigate the regulation of the stress neurohormone corticotropin releasing factor (CRF) system and of the nociceptin/orphanin FQ (N/OFQ) system genes in selective rat brain regions, using our animal model. Food restriction by itself might be responsible in the hypothalamus for the downregulation on mRNA levels of CRF-1 receptor (CRF-1R), N/OFQ as well as its receptor NOP. For the latter, this alteration might be due to selective histone modification changes. Instead, CRF gene appears to be upregulated in the hypothalamus and in the ventral tegmental area only when rats are food restricted and exposed to frustration stress and, of relevance, these changes appear to be due to a reduction in DNA methylation at gene promoters. Moreover, CRF-1R mRNA resulted also to be differentially regulated in these two brain regions. Our data add information on altered N/OFQ and CRF signalling in food restriction and under stressful conditions, and provide insight on the use of this model of binge eating for the study of epigenetic modifications in controlled genetic and environmental backgrounds. ACKNOWLEDGMENTS: The work was supported by the Italian Ministry of University and Research under grant FIRB-RBFR12DELS to CC and CDA. The authors declare no competing financial interests.

Epigenetic regulation of nociceptin/orphanin FQ and corticotropin-releasing factor system genes in frustration stress-induced binge-like palatable food consumption

Giusepponi Maria Elena;Micioni Di Bonaventura Maria Vittoria;Ciccocioppo Roberto;Cifani Carlo
2015-01-01

Abstract

Evidence suggests that binge eating may be caused by a unique interaction between dieting and stress. We developed a binge-eating model in which female rats with a history of intermittent food restriction show binge-like palatable food consumption after 15 min exposure to the sight of the palatable food (frustration stress). Aim of the present study was to investigate the regulation of the stress neurohormone corticotropin releasing factor (CRF) system and of the nociceptin/orphanin FQ (N/OFQ) system genes in selective rat brain regions, using our animal model. Food restriction by itself might be responsible in the hypothalamus for the downregulation on mRNA levels of CRF-1 receptor (CRF-1R), N/OFQ as well as its receptor NOP. For the latter, this alteration might be due to selective histone modification changes. Instead, CRF gene appears to be upregulated in the hypothalamus and in the ventral tegmental area only when rats are food restricted and exposed to frustration stress and, of relevance, these changes appear to be due to a reduction in DNA methylation at gene promoters. Moreover, CRF-1R mRNA resulted also to be differentially regulated in these two brain regions. Our data add information on altered N/OFQ and CRF signalling in food restriction and under stressful conditions, and provide insight on the use of this model of binge eating for the study of epigenetic modifications in controlled genetic and environmental backgrounds. ACKNOWLEDGMENTS: The work was supported by the Italian Ministry of University and Research under grant FIRB-RBFR12DELS to CC and CDA. The authors declare no competing financial interests.
2015
275
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/405341
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