Exploring the acute effects of running on cerebral blood flow and food cue reactivity in healthy young men using functional magnetic resonance imaging
Acute exercise suppresses appetite and alters food‐cue reactivity, but the extent exercise‐induced changes in cerebral blood flow (CBF) influences the blood‐oxygen‐level‐dependent (BOLD) signal during appetite‐related paradigms is not known. This study examined the impact of acute running on visual...
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creator | Thackray, Alice E. Hinton, Elanor C. Alanazi, Turki M. Dera, Abdulrahman M. Fujihara, Kyoko Hamilton‐Shield, Julian P. King, James A. Lithander, Fiona E. Miyashita, Masashi Thompson, Julie Morgan, Paul S. Davies, Melanie J. Stensel, David J. |
description | Acute exercise suppresses appetite and alters food‐cue reactivity, but the extent exercise‐induced changes in cerebral blood flow (CBF) influences the blood‐oxygen‐level‐dependent (BOLD) signal during appetite‐related paradigms is not known. This study examined the impact of acute running on visual food‐cue reactivity and explored whether such responses are influenced by CBF variability. In a randomised crossover design, 23 men (mean ± SD: 24 ± 4 years, 22.9 ± 2.1 kg/m2) completed fMRI scans before and after 60 min of running (68% ± 3% peak oxygen uptake) or rest (control). Five‐minute pseudo‐continuous arterial spin labelling fMRI scans were conducted for CBF assessment before and at four consecutive repeat acquisitions after exercise/rest. BOLD‐fMRI was acquired during a food‐cue reactivity task before and 28 min after exercise/rest. Food‐cue reactivity analysis was performed with and without CBF adjustment. Subjective appetite ratings were assessed before, during and after exercise/rest. Exercise CBF was higher in grey matter, the posterior insula and in the region of the amygdala/hippocampus, and lower in the medial orbitofrontal cortex and dorsal striatum than control (main effect trial p ≤ .018). No time‐by‐trial interactions for CBF were identified (p ≥ .087). Exercise induced moderate‐to‐large reductions in subjective appetite ratings (Cohen's d = 0.53–0.84; p ≤ .024) and increased food‐cue reactivity in the paracingulate gyrus, hippocampus, precuneous cortex, frontal pole and posterior cingulate gyrus. Accounting for CBF variability did not markedly alter detection of exercise‐induced BOLD signal changes. Acute running evoked overall changes in CBF that were not time dependent and increased food‐cue reactivity in regions implicated in attention, anticipation of reward, and episodic memory independent of CBF.
We investigated the impact of a single running bout on cerebral blood flow (CBF) and food cue reactivity using functional magnetic resonance imaging (fMRI) in healthy men. Running did not alter the time‐course of grey matter or regional CBF up to 30 min after exercise cessation but increased food cue reactivity in brain regions implicated in attention, reward and episodic memory retrieval. Exercise‐related BOLD signal changes were detected in the presence of underlying CBF. |
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We investigated the impact of a single running bout on cerebral blood flow (CBF) and food cue reactivity using functional magnetic resonance imaging (fMRI) in healthy men. Running did not alter the time‐course of grey matter or regional CBF up to 30 min after exercise cessation but increased food cue reactivity in brain regions implicated in attention, reward and episodic memory retrieval. Exercise‐related BOLD signal changes were detected in the presence of underlying CBF.</description><identifier>ISSN: 1065-9471</identifier><identifier>EISSN: 1097-0193</identifier><identifier>DOI: 10.1002/hbm.26314</identifier><identifier>PMID: 37145965</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Acute effects ; Amygdala ; Appetite ; Blood flow ; Body fat ; Brain ; Brain - physiology ; Caudate-putamen ; Cerebral blood flow ; Cerebrovascular Circulation - physiology ; Cortex (frontal) ; Cross-Over Studies ; Cues ; Eating behavior ; Exercise ; fMRI ; Food ; food cue reactivity ; Functional magnetic resonance imaging ; Hippocampus ; Humans ; Labeling ; Laboratories ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Maximum oxygen consumption ; Metabolism ; Neostriatum ; Neuroimaging ; Oxygen ; Oxygen consumption ; Oxygen uptake ; Physical fitness ; Physical training ; Questionnaires ; Ratings ; Running ; Spin labeling ; Substantia grisea ; Time dependence ; Variability ; Visual stimuli</subject><ispartof>Human brain mapping, 2023-06, Vol.44 (9), p.3815-3832</ispartof><rights>2023 The Authors. published by Wiley Periodicals LLC.</rights><rights>2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4444-5498c70605c3248c73e9e03a980fcc057faef1e87225853cd3aba0536141100e3</citedby><cites>FETCH-LOGICAL-c4444-5498c70605c3248c73e9e03a980fcc057faef1e87225853cd3aba0536141100e3</cites><orcidid>0000-0003-2793-8552 ; 0000-0002-7800-3207 ; 0000-0002-8174-9173 ; 0000-0002-5870-1446 ; 0000-0003-2601-7575 ; 0000-0002-7656-641X ; 0000-0001-9119-8590 ; 0000-0003-4542-7924 ; 0000-0001-6378-6977</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203797/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203797/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37145965$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thackray, Alice E.</creatorcontrib><creatorcontrib>Hinton, Elanor C.</creatorcontrib><creatorcontrib>Alanazi, Turki M.</creatorcontrib><creatorcontrib>Dera, Abdulrahman M.</creatorcontrib><creatorcontrib>Fujihara, Kyoko</creatorcontrib><creatorcontrib>Hamilton‐Shield, Julian P.</creatorcontrib><creatorcontrib>King, James A.</creatorcontrib><creatorcontrib>Lithander, Fiona E.</creatorcontrib><creatorcontrib>Miyashita, Masashi</creatorcontrib><creatorcontrib>Thompson, Julie</creatorcontrib><creatorcontrib>Morgan, Paul S.</creatorcontrib><creatorcontrib>Davies, Melanie J.</creatorcontrib><creatorcontrib>Stensel, David J.</creatorcontrib><title>Exploring the acute effects of running on cerebral blood flow and food cue reactivity in healthy young men using functional magnetic resonance imaging</title><title>Human brain mapping</title><addtitle>Hum Brain Mapp</addtitle><description>Acute exercise suppresses appetite and alters food‐cue reactivity, but the extent exercise‐induced changes in cerebral blood flow (CBF) influences the blood‐oxygen‐level‐dependent (BOLD) signal during appetite‐related paradigms is not known. This study examined the impact of acute running on visual food‐cue reactivity and explored whether such responses are influenced by CBF variability. In a randomised crossover design, 23 men (mean ± SD: 24 ± 4 years, 22.9 ± 2.1 kg/m2) completed fMRI scans before and after 60 min of running (68% ± 3% peak oxygen uptake) or rest (control). Five‐minute pseudo‐continuous arterial spin labelling fMRI scans were conducted for CBF assessment before and at four consecutive repeat acquisitions after exercise/rest. BOLD‐fMRI was acquired during a food‐cue reactivity task before and 28 min after exercise/rest. Food‐cue reactivity analysis was performed with and without CBF adjustment. Subjective appetite ratings were assessed before, during and after exercise/rest. Exercise CBF was higher in grey matter, the posterior insula and in the region of the amygdala/hippocampus, and lower in the medial orbitofrontal cortex and dorsal striatum than control (main effect trial p ≤ .018). No time‐by‐trial interactions for CBF were identified (p ≥ .087). Exercise induced moderate‐to‐large reductions in subjective appetite ratings (Cohen's d = 0.53–0.84; p ≤ .024) and increased food‐cue reactivity in the paracingulate gyrus, hippocampus, precuneous cortex, frontal pole and posterior cingulate gyrus. Accounting for CBF variability did not markedly alter detection of exercise‐induced BOLD signal changes. Acute running evoked overall changes in CBF that were not time dependent and increased food‐cue reactivity in regions implicated in attention, anticipation of reward, and episodic memory independent of CBF.
We investigated the impact of a single running bout on cerebral blood flow (CBF) and food cue reactivity using functional magnetic resonance imaging (fMRI) in healthy men. Running did not alter the time‐course of grey matter or regional CBF up to 30 min after exercise cessation but increased food cue reactivity in brain regions implicated in attention, reward and episodic memory retrieval. Exercise‐related BOLD signal changes were detected in the presence of underlying CBF.</description><subject>Acute effects</subject><subject>Amygdala</subject><subject>Appetite</subject><subject>Blood flow</subject><subject>Body fat</subject><subject>Brain</subject><subject>Brain - physiology</subject><subject>Caudate-putamen</subject><subject>Cerebral blood flow</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>Cortex (frontal)</subject><subject>Cross-Over Studies</subject><subject>Cues</subject><subject>Eating behavior</subject><subject>Exercise</subject><subject>fMRI</subject><subject>Food</subject><subject>food cue reactivity</subject><subject>Functional magnetic resonance imaging</subject><subject>Hippocampus</subject><subject>Humans</subject><subject>Labeling</subject><subject>Laboratories</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Maximum oxygen consumption</subject><subject>Metabolism</subject><subject>Neostriatum</subject><subject>Neuroimaging</subject><subject>Oxygen</subject><subject>Oxygen consumption</subject><subject>Oxygen uptake</subject><subject>Physical fitness</subject><subject>Physical training</subject><subject>Questionnaires</subject><subject>Ratings</subject><subject>Running</subject><subject>Spin labeling</subject><subject>Substantia grisea</subject><subject>Time dependence</subject><subject>Variability</subject><subject>Visual stimuli</subject><issn>1065-9471</issn><issn>1097-0193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kctu1TAQhiMEoqWw4AWQJTawSGvHcS4rVKpCkYrYwNpyfMYnrhL74EtLXoTnZXJOqQAJS5bHnm9-jecvipeMnjJKq7NxmE-rhrP6UXHMaN-WlPX88Ro3ouzrlh0Vz2K8oZQxQdnT4oi3rBZ9I46Ln5c_dpMP1m1JGoEonRMQMAZ0isQbErJza9I7oiHAENREhsn7DTGTvyPKYbDedAYSQOlkb21aiHVkBDWlcSGLz1g_gyM5rkomO6S8Q6FZbR0kq7Ey4oPTQCy-IfW8eGLUFOHF_XlSfPtw-fXiqrz-8vHTxfl1qWtcpaj7Tre0oULzqsaQQw-Uq76jRmsqWqPAMOjaqhKd4HrD1aCo4A2rGU4O-Enx7qC7y8MMGw0u4Q_lLmAfYZFeWfl3xtlRbv2tZLSivO1bVHhzrxD89wwxydlGDdOkHPgcZdWhIxWle_T1P-iNzwEHsafaqsFdI_X2QOngYwxgHrphVK52S7Rb7u1G9tWf7T-Qv_1F4OwA3NkJlv8ryav3nw-SvwD8craO</recordid><startdate>20230615</startdate><enddate>20230615</enddate><creator>Thackray, Alice E.</creator><creator>Hinton, Elanor C.</creator><creator>Alanazi, Turki M.</creator><creator>Dera, Abdulrahman M.</creator><creator>Fujihara, Kyoko</creator><creator>Hamilton‐Shield, Julian P.</creator><creator>King, James A.</creator><creator>Lithander, Fiona E.</creator><creator>Miyashita, Masashi</creator><creator>Thompson, Julie</creator><creator>Morgan, Paul S.</creator><creator>Davies, Melanie J.</creator><creator>Stensel, David J.</creator><general>John Wiley & Sons, Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2793-8552</orcidid><orcidid>https://orcid.org/0000-0002-7800-3207</orcidid><orcidid>https://orcid.org/0000-0002-8174-9173</orcidid><orcidid>https://orcid.org/0000-0002-5870-1446</orcidid><orcidid>https://orcid.org/0000-0003-2601-7575</orcidid><orcidid>https://orcid.org/0000-0002-7656-641X</orcidid><orcidid>https://orcid.org/0000-0001-9119-8590</orcidid><orcidid>https://orcid.org/0000-0003-4542-7924</orcidid><orcidid>https://orcid.org/0000-0001-6378-6977</orcidid></search><sort><creationdate>20230615</creationdate><title>Exploring the acute effects of running on cerebral blood flow and food cue reactivity in healthy young men using functional magnetic resonance imaging</title><author>Thackray, Alice E. ; Hinton, Elanor C. ; Alanazi, Turki M. ; Dera, Abdulrahman M. ; Fujihara, Kyoko ; Hamilton‐Shield, Julian P. ; King, James A. ; Lithander, Fiona E. ; Miyashita, Masashi ; Thompson, Julie ; Morgan, Paul S. ; Davies, Melanie J. ; Stensel, David J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4444-5498c70605c3248c73e9e03a980fcc057faef1e87225853cd3aba0536141100e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acute effects</topic><topic>Amygdala</topic><topic>Appetite</topic><topic>Blood flow</topic><topic>Body fat</topic><topic>Brain</topic><topic>Brain - physiology</topic><topic>Caudate-putamen</topic><topic>Cerebral blood flow</topic><topic>Cerebrovascular Circulation - physiology</topic><topic>Cortex (frontal)</topic><topic>Cross-Over Studies</topic><topic>Cues</topic><topic>Eating behavior</topic><topic>Exercise</topic><topic>fMRI</topic><topic>Food</topic><topic>food cue reactivity</topic><topic>Functional magnetic resonance imaging</topic><topic>Hippocampus</topic><topic>Humans</topic><topic>Labeling</topic><topic>Laboratories</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Maximum oxygen consumption</topic><topic>Metabolism</topic><topic>Neostriatum</topic><topic>Neuroimaging</topic><topic>Oxygen</topic><topic>Oxygen consumption</topic><topic>Oxygen uptake</topic><topic>Physical fitness</topic><topic>Physical training</topic><topic>Questionnaires</topic><topic>Ratings</topic><topic>Running</topic><topic>Spin labeling</topic><topic>Substantia grisea</topic><topic>Time dependence</topic><topic>Variability</topic><topic>Visual stimuli</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thackray, Alice E.</creatorcontrib><creatorcontrib>Hinton, Elanor C.</creatorcontrib><creatorcontrib>Alanazi, Turki M.</creatorcontrib><creatorcontrib>Dera, Abdulrahman M.</creatorcontrib><creatorcontrib>Fujihara, Kyoko</creatorcontrib><creatorcontrib>Hamilton‐Shield, Julian P.</creatorcontrib><creatorcontrib>King, James A.</creatorcontrib><creatorcontrib>Lithander, Fiona E.</creatorcontrib><creatorcontrib>Miyashita, Masashi</creatorcontrib><creatorcontrib>Thompson, Julie</creatorcontrib><creatorcontrib>Morgan, Paul S.</creatorcontrib><creatorcontrib>Davies, Melanie J.</creatorcontrib><creatorcontrib>Stensel, David J.</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Human brain mapping</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thackray, Alice E.</au><au>Hinton, Elanor C.</au><au>Alanazi, Turki M.</au><au>Dera, Abdulrahman M.</au><au>Fujihara, Kyoko</au><au>Hamilton‐Shield, Julian P.</au><au>King, James A.</au><au>Lithander, Fiona E.</au><au>Miyashita, Masashi</au><au>Thompson, Julie</au><au>Morgan, Paul S.</au><au>Davies, Melanie J.</au><au>Stensel, David J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring the acute effects of running on cerebral blood flow and food cue reactivity in healthy young men using functional magnetic resonance imaging</atitle><jtitle>Human brain mapping</jtitle><addtitle>Hum Brain Mapp</addtitle><date>2023-06-15</date><risdate>2023</risdate><volume>44</volume><issue>9</issue><spage>3815</spage><epage>3832</epage><pages>3815-3832</pages><issn>1065-9471</issn><eissn>1097-0193</eissn><abstract>Acute exercise suppresses appetite and alters food‐cue reactivity, but the extent exercise‐induced changes in cerebral blood flow (CBF) influences the blood‐oxygen‐level‐dependent (BOLD) signal during appetite‐related paradigms is not known. This study examined the impact of acute running on visual food‐cue reactivity and explored whether such responses are influenced by CBF variability. In a randomised crossover design, 23 men (mean ± SD: 24 ± 4 years, 22.9 ± 2.1 kg/m2) completed fMRI scans before and after 60 min of running (68% ± 3% peak oxygen uptake) or rest (control). Five‐minute pseudo‐continuous arterial spin labelling fMRI scans were conducted for CBF assessment before and at four consecutive repeat acquisitions after exercise/rest. BOLD‐fMRI was acquired during a food‐cue reactivity task before and 28 min after exercise/rest. Food‐cue reactivity analysis was performed with and without CBF adjustment. Subjective appetite ratings were assessed before, during and after exercise/rest. Exercise CBF was higher in grey matter, the posterior insula and in the region of the amygdala/hippocampus, and lower in the medial orbitofrontal cortex and dorsal striatum than control (main effect trial p ≤ .018). No time‐by‐trial interactions for CBF were identified (p ≥ .087). Exercise induced moderate‐to‐large reductions in subjective appetite ratings (Cohen's d = 0.53–0.84; p ≤ .024) and increased food‐cue reactivity in the paracingulate gyrus, hippocampus, precuneous cortex, frontal pole and posterior cingulate gyrus. Accounting for CBF variability did not markedly alter detection of exercise‐induced BOLD signal changes. Acute running evoked overall changes in CBF that were not time dependent and increased food‐cue reactivity in regions implicated in attention, anticipation of reward, and episodic memory independent of CBF.
We investigated the impact of a single running bout on cerebral blood flow (CBF) and food cue reactivity using functional magnetic resonance imaging (fMRI) in healthy men. Running did not alter the time‐course of grey matter or regional CBF up to 30 min after exercise cessation but increased food cue reactivity in brain regions implicated in attention, reward and episodic memory retrieval. Exercise‐related BOLD signal changes were detected in the presence of underlying CBF.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>37145965</pmid><doi>10.1002/hbm.26314</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-2793-8552</orcidid><orcidid>https://orcid.org/0000-0002-7800-3207</orcidid><orcidid>https://orcid.org/0000-0002-8174-9173</orcidid><orcidid>https://orcid.org/0000-0002-5870-1446</orcidid><orcidid>https://orcid.org/0000-0003-2601-7575</orcidid><orcidid>https://orcid.org/0000-0002-7656-641X</orcidid><orcidid>https://orcid.org/0000-0001-9119-8590</orcidid><orcidid>https://orcid.org/0000-0003-4542-7924</orcidid><orcidid>https://orcid.org/0000-0001-6378-6977</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute effects Amygdala Appetite Blood flow Body fat Brain Brain - physiology Caudate-putamen Cerebral blood flow Cerebrovascular Circulation - physiology Cortex (frontal) Cross-Over Studies Cues Eating behavior Exercise fMRI Food food cue reactivity Functional magnetic resonance imaging Hippocampus Humans Labeling Laboratories Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Maximum oxygen consumption Metabolism Neostriatum Neuroimaging Oxygen Oxygen consumption Oxygen uptake Physical fitness Physical training Questionnaires Ratings Running Spin labeling Substantia grisea Time dependence Variability Visual stimuli |
title | Exploring the acute effects of running on cerebral blood flow and food cue reactivity in healthy young men using functional magnetic resonance imaging |
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