Cargando…

Inhibition of food craving is a metabolically active process in the brain in obese men

OBJECTIVE: Obesity is associated with impaired inhibitory control over food intake. We hypothesized that the neural circuitry underlying inhibition of food craving would be impaired in obesity. Here we assessed whether obese men show altered brain responses during attempted cognitive inhibition of c...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Gene-Jack, Shokri Kojori, Ehsan, Yuan, Kai, Wiers, Corinde E., Manza, Peter, Wong, Christopher T., Fowler, Joanna S., Volkow, Nora D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046524/
https://www.ncbi.nlm.nih.gov/pubmed/31740725
http://dx.doi.org/10.1038/s41366-019-0484-z
_version_ 1783501963500978176
author Wang, Gene-Jack
Shokri Kojori, Ehsan
Yuan, Kai
Wiers, Corinde E.
Manza, Peter
Wong, Christopher T.
Fowler, Joanna S.
Volkow, Nora D.
author_facet Wang, Gene-Jack
Shokri Kojori, Ehsan
Yuan, Kai
Wiers, Corinde E.
Manza, Peter
Wong, Christopher T.
Fowler, Joanna S.
Volkow, Nora D.
author_sort Wang, Gene-Jack
collection PubMed
description OBJECTIVE: Obesity is associated with impaired inhibitory control over food intake. We hypothesized that the neural circuitry underlying inhibition of food craving would be impaired in obesity. Here we assessed whether obese men show altered brain responses during attempted cognitive inhibition of craving when exposed to food cues. METHODS: Sixteen obese men (32 ± 8.7 years old, BMI = 38.6 ± 7.2) were compared with 11 age-matched non-obese men (BMI 24.2 ± 2.5) using PET and FDG. Brain glucose metabolism was evaluated in a food deprived state: no food stimulation, food stimulation with no inhibition (NI), and food stimulation with attempted inhibition (AI), each on a separate day. Individualized favorite food items were presented prior to and after FDG injection for 40 min. For AI, participants were asked to attempt to inhibit their desire for the food presented. Self-reports for hunger and food desire were recorded. RESULTS: Food stimulation compared with no stimulation increased glucose metabolism in inferior and superior frontal gyrus, default mode network and cerebellum, in both groups. For both groups, AI compared with NI-suppressed metabolism in right subgenual anterior cingulate, orbitofrontal areas, bilateral insula, and temporal gyri. There was a stimulation-by-group interaction effect in obese (but not in non-obese) men showing increased metabolism in pregenual anterior cingulate cortex (pgACC) and caudate during AI relative to NI. Changes in the food desire from NI to AI correlated negatively with changes in metabolism in pgACC/caudate in obese but not in non-obese men. CONCLUSIONS: Obese men showed higher activation in pgACC/caudate, which are regions involved with self-regulation and emotion/reward during AI. Behavioral associations suggest that successful AI is an active process requiring more energy in obese but not in non-obese men. The additional required effort to increase cognitive control in response to food stimulation in obese compared with non-obese men may contribute to their uncontrolled eating behavior.
format Online
Article
Text
id pubmed-7046524
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70465242020-03-04 Inhibition of food craving is a metabolically active process in the brain in obese men Wang, Gene-Jack Shokri Kojori, Ehsan Yuan, Kai Wiers, Corinde E. Manza, Peter Wong, Christopher T. Fowler, Joanna S. Volkow, Nora D. Int J Obes (Lond) Article OBJECTIVE: Obesity is associated with impaired inhibitory control over food intake. We hypothesized that the neural circuitry underlying inhibition of food craving would be impaired in obesity. Here we assessed whether obese men show altered brain responses during attempted cognitive inhibition of craving when exposed to food cues. METHODS: Sixteen obese men (32 ± 8.7 years old, BMI = 38.6 ± 7.2) were compared with 11 age-matched non-obese men (BMI 24.2 ± 2.5) using PET and FDG. Brain glucose metabolism was evaluated in a food deprived state: no food stimulation, food stimulation with no inhibition (NI), and food stimulation with attempted inhibition (AI), each on a separate day. Individualized favorite food items were presented prior to and after FDG injection for 40 min. For AI, participants were asked to attempt to inhibit their desire for the food presented. Self-reports for hunger and food desire were recorded. RESULTS: Food stimulation compared with no stimulation increased glucose metabolism in inferior and superior frontal gyrus, default mode network and cerebellum, in both groups. For both groups, AI compared with NI-suppressed metabolism in right subgenual anterior cingulate, orbitofrontal areas, bilateral insula, and temporal gyri. There was a stimulation-by-group interaction effect in obese (but not in non-obese) men showing increased metabolism in pregenual anterior cingulate cortex (pgACC) and caudate during AI relative to NI. Changes in the food desire from NI to AI correlated negatively with changes in metabolism in pgACC/caudate in obese but not in non-obese men. CONCLUSIONS: Obese men showed higher activation in pgACC/caudate, which are regions involved with self-regulation and emotion/reward during AI. Behavioral associations suggest that successful AI is an active process requiring more energy in obese but not in non-obese men. The additional required effort to increase cognitive control in response to food stimulation in obese compared with non-obese men may contribute to their uncontrolled eating behavior. Nature Publishing Group UK 2019-11-18 2020 /pmc/articles/PMC7046524/ /pubmed/31740725 http://dx.doi.org/10.1038/s41366-019-0484-z Text en © The Author(s), under exclusive licence to Springer Nature Limited 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Gene-Jack
Shokri Kojori, Ehsan
Yuan, Kai
Wiers, Corinde E.
Manza, Peter
Wong, Christopher T.
Fowler, Joanna S.
Volkow, Nora D.
Inhibition of food craving is a metabolically active process in the brain in obese men
title Inhibition of food craving is a metabolically active process in the brain in obese men
title_full Inhibition of food craving is a metabolically active process in the brain in obese men
title_fullStr Inhibition of food craving is a metabolically active process in the brain in obese men
title_full_unstemmed Inhibition of food craving is a metabolically active process in the brain in obese men
title_short Inhibition of food craving is a metabolically active process in the brain in obese men
title_sort inhibition of food craving is a metabolically active process in the brain in obese men
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046524/
https://www.ncbi.nlm.nih.gov/pubmed/31740725
http://dx.doi.org/10.1038/s41366-019-0484-z
work_keys_str_mv AT wanggenejack inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen
AT shokrikojoriehsan inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen
AT yuankai inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen
AT wierscorindee inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen
AT manzapeter inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen
AT wongchristophert inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen
AT fowlerjoannas inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen
AT volkownorad inhibitionoffoodcravingisametabolicallyactiveprocessinthebraininobesemen