Cargando…

Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents

Ghrelin, an orexigenic hormone released from the empty stomach, provides a gut–brain signal that promotes many appetitive behaviours, including anticipatory and goal‐directed behaviours for palatable treats high in sugar and/or fat. In the present study, we aimed to determine whether ghrelin is able...

Descripción completa

Detalles Bibliográficos
Autores principales: Bake, T., Hellgren, K. T., Dickson, S. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434925/
https://www.ncbi.nlm.nih.gov/pubmed/28219000
http://dx.doi.org/10.1111/jne.12463
_version_ 1783237142520004608
author Bake, T.
Hellgren, K. T.
Dickson, S. L.
author_facet Bake, T.
Hellgren, K. T.
Dickson, S. L.
author_sort Bake, T.
collection PubMed
description Ghrelin, an orexigenic hormone released from the empty stomach, provides a gut–brain signal that promotes many appetitive behaviours, including anticipatory and goal‐directed behaviours for palatable treats high in sugar and/or fat. In the present study, we aimed to determine whether ghrelin is able to influence and/or may even have a role in binge‐like eating behaviour in rodents. Accordingly, we used a palatable scheduled feeding (PSF) paradigm in which ad lib. chow‐fed rodents are trained to ‘binge’ on a high‐fat diet (HFD) offered each day for a limited period of 2 hours. After 2 weeks of habituation to this paradigm, on the test day and immediately prior to the 2‐hour PSF, rats were administered ghrelin or vehicle solution by the i.c.v. route. Remarkably and unexpectedly, during the palatable scheduled feed, when rats normally only binge on the HFD, those injected with i.c.v. ghrelin started to eat more chow and chow intake remained above baseline for the rest of the 24‐hour day. We identify the ventral tegmental area (VTA) (a key brain area involved in food reward) as a substrate involved because these effects could be reproduced, in part, by intra‐VTA delivery of ghrelin. Fasting, which increases endogenous ghrelin, immediately prior to a palatable schedule feed also increased chow intake during/after the schedule feed but, in contrast to ghrelin injection, did not reduce HFD intake. Chronic continuous central ghrelin infusion over several weeks enhanced binge‐like behaviour in palatable schedule fed rats. Over a 4‐week period, GHS‐R1A‐KO mice were able to adapt and maintain large meals of HFD in a manner similar to wild‐type mice, suggesting that ghrelin signalling may not have a critical role in the acquisition or maintenance in this kind of feeding behaviour. In conclusion, ghrelin appears to act as a modulating factor for binge‐like eating behaviour by shifting food preference towards a more nutritious choice (from HFD to chow), with these effects being somewhat divergent from fasting.
format Online
Article
Text
id pubmed-5434925
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-54349252018-04-12 Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents Bake, T. Hellgren, K. T. Dickson, S. L. J Neuroendocrinol Original Articles Ghrelin, an orexigenic hormone released from the empty stomach, provides a gut–brain signal that promotes many appetitive behaviours, including anticipatory and goal‐directed behaviours for palatable treats high in sugar and/or fat. In the present study, we aimed to determine whether ghrelin is able to influence and/or may even have a role in binge‐like eating behaviour in rodents. Accordingly, we used a palatable scheduled feeding (PSF) paradigm in which ad lib. chow‐fed rodents are trained to ‘binge’ on a high‐fat diet (HFD) offered each day for a limited period of 2 hours. After 2 weeks of habituation to this paradigm, on the test day and immediately prior to the 2‐hour PSF, rats were administered ghrelin or vehicle solution by the i.c.v. route. Remarkably and unexpectedly, during the palatable scheduled feed, when rats normally only binge on the HFD, those injected with i.c.v. ghrelin started to eat more chow and chow intake remained above baseline for the rest of the 24‐hour day. We identify the ventral tegmental area (VTA) (a key brain area involved in food reward) as a substrate involved because these effects could be reproduced, in part, by intra‐VTA delivery of ghrelin. Fasting, which increases endogenous ghrelin, immediately prior to a palatable schedule feed also increased chow intake during/after the schedule feed but, in contrast to ghrelin injection, did not reduce HFD intake. Chronic continuous central ghrelin infusion over several weeks enhanced binge‐like behaviour in palatable schedule fed rats. Over a 4‐week period, GHS‐R1A‐KO mice were able to adapt and maintain large meals of HFD in a manner similar to wild‐type mice, suggesting that ghrelin signalling may not have a critical role in the acquisition or maintenance in this kind of feeding behaviour. In conclusion, ghrelin appears to act as a modulating factor for binge‐like eating behaviour by shifting food preference towards a more nutritious choice (from HFD to chow), with these effects being somewhat divergent from fasting. John Wiley and Sons Inc. 2017-04-02 2017-04 /pmc/articles/PMC5434925/ /pubmed/28219000 http://dx.doi.org/10.1111/jne.12463 Text en © 2017 The Authors. Journal of Neuroendocrinology published by John Wiley & Sons Ltd on behalf of British Society for Neuroendocrinology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Bake, T.
Hellgren, K. T.
Dickson, S. L.
Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents
title Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents
title_full Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents
title_fullStr Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents
title_full_unstemmed Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents
title_short Acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents
title_sort acute ghrelin changes food preference from a high‐fat diet to chow during binge‐like eating in rodents
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434925/
https://www.ncbi.nlm.nih.gov/pubmed/28219000
http://dx.doi.org/10.1111/jne.12463
work_keys_str_mv AT baket acuteghrelinchangesfoodpreferencefromahighfatdiettochowduringbingelikeeatinginrodents
AT hellgrenkt acuteghrelinchangesfoodpreferencefromahighfatdiettochowduringbingelikeeatinginrodents
AT dicksonsl acuteghrelinchangesfoodpreferencefromahighfatdiettochowduringbingelikeeatinginrodents