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Fasting enhances extinction retention and prevents the return of fear in humans

Fear is prone to return following extinction that is the basis of exposure therapy for fear-related disorders. Manipulations that enhance the extinction process can be beneficial for treatment. Animal studies have shown that fasting or caloric restriction can enhance extinction and inhibit the retur...

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Autores principales: Shi, Le, Deng, Jiahui, Chen, Sijing, Que, Jianyu, Sun, Yekun, Wang, Zhong, Guo, Xiaojie, Han, Ying, Zhou, Yuxin, Zhang, Xiujun, Xie, Wen, Lin, Xiao, Shi, Jie, Lu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177454/
https://www.ncbi.nlm.nih.gov/pubmed/30301955
http://dx.doi.org/10.1038/s41398-018-0260-1
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author Shi, Le
Deng, Jiahui
Chen, Sijing
Que, Jianyu
Sun, Yekun
Wang, Zhong
Guo, Xiaojie
Han, Ying
Zhou, Yuxin
Zhang, Xiujun
Xie, Wen
Lin, Xiao
Shi, Jie
Lu, Lin
author_facet Shi, Le
Deng, Jiahui
Chen, Sijing
Que, Jianyu
Sun, Yekun
Wang, Zhong
Guo, Xiaojie
Han, Ying
Zhou, Yuxin
Zhang, Xiujun
Xie, Wen
Lin, Xiao
Shi, Jie
Lu, Lin
author_sort Shi, Le
collection PubMed
description Fear is prone to return following extinction that is the basis of exposure therapy for fear-related disorders. Manipulations that enhance the extinction process can be beneficial for treatment. Animal studies have shown that fasting or caloric restriction can enhance extinction and inhibit the return of fear. The present study examined the effects of fasting on fear acquisition, extinction, and the return of fear in humans. One hundred and twenty-five male participants were randomized into a fasting group and food group and exposed to a Pavlovian fear conditioning paradigm. Changes in plasma cortisol and ghrelin levels were examined using enzyme-linked immunosorbent assays. One-night fasting had no effect on fear acquisition but enhanced fear extinction retention and prevented the return of fear, and this effect persisted for at least 6 months. This procedure was also effective for remote fear memory. Plasma ghrelin levels were elevated after fasting and had a negative relationship with the fear response in spontaneous recovery test. However, overnight fasting did not affect cortisol levels. These findings indicate that fasting enhances extinction retention and prevents the return of fear, without influencing fear memory formation. We propose that this novel procedure may open new avenues for promoting extinction-based therapies for fear-related disorders.
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spelling pubmed-61774542018-10-11 Fasting enhances extinction retention and prevents the return of fear in humans Shi, Le Deng, Jiahui Chen, Sijing Que, Jianyu Sun, Yekun Wang, Zhong Guo, Xiaojie Han, Ying Zhou, Yuxin Zhang, Xiujun Xie, Wen Lin, Xiao Shi, Jie Lu, Lin Transl Psychiatry Article Fear is prone to return following extinction that is the basis of exposure therapy for fear-related disorders. Manipulations that enhance the extinction process can be beneficial for treatment. Animal studies have shown that fasting or caloric restriction can enhance extinction and inhibit the return of fear. The present study examined the effects of fasting on fear acquisition, extinction, and the return of fear in humans. One hundred and twenty-five male participants were randomized into a fasting group and food group and exposed to a Pavlovian fear conditioning paradigm. Changes in plasma cortisol and ghrelin levels were examined using enzyme-linked immunosorbent assays. One-night fasting had no effect on fear acquisition but enhanced fear extinction retention and prevented the return of fear, and this effect persisted for at least 6 months. This procedure was also effective for remote fear memory. Plasma ghrelin levels were elevated after fasting and had a negative relationship with the fear response in spontaneous recovery test. However, overnight fasting did not affect cortisol levels. These findings indicate that fasting enhances extinction retention and prevents the return of fear, without influencing fear memory formation. We propose that this novel procedure may open new avenues for promoting extinction-based therapies for fear-related disorders. Nature Publishing Group UK 2018-10-09 /pmc/articles/PMC6177454/ /pubmed/30301955 http://dx.doi.org/10.1038/s41398-018-0260-1 Text en © The Author(s) 2018 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
Shi, Le
Deng, Jiahui
Chen, Sijing
Que, Jianyu
Sun, Yekun
Wang, Zhong
Guo, Xiaojie
Han, Ying
Zhou, Yuxin
Zhang, Xiujun
Xie, Wen
Lin, Xiao
Shi, Jie
Lu, Lin
Fasting enhances extinction retention and prevents the return of fear in humans
title Fasting enhances extinction retention and prevents the return of fear in humans
title_full Fasting enhances extinction retention and prevents the return of fear in humans
title_fullStr Fasting enhances extinction retention and prevents the return of fear in humans
title_full_unstemmed Fasting enhances extinction retention and prevents the return of fear in humans
title_short Fasting enhances extinction retention and prevents the return of fear in humans
title_sort fasting enhances extinction retention and prevents the return of fear in humans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177454/
https://www.ncbi.nlm.nih.gov/pubmed/30301955
http://dx.doi.org/10.1038/s41398-018-0260-1
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