Magnetic resonance imaging biomarkers of exercise‐induced improvement of oxidative stress and inflammation in the brain of old high‐fat‐fed ApoE−/− mice
Key points Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress. Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation. In this study, exercise training...
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Veröffentlicht in: | The Journal of physiology 2016-12, Vol.594 (23), p.6969-6985 |
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creator | Chirico, Erica N. Di Cataldo, Vanessa Chauveau, Fabien Geloën, Alain Patsouris, David Thézé, Benoît Martin, Cyril Vidal, Hubert Rieusset, Jennifer Pialoux, Vincent Canet‐Soulas, Emmanuelle |
description | Key points
Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress.
Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation.
In this study, exercise training reduced magnetic resonance imaging‐detected abnormalities, insulin resistance and markers of oxidative stress and inflammation in old ApoE−/− mice.
Our results demonstrate the protective effect of exercise on neurovascular damage in the ageing brain of ApoE−/− mice.
Vascular brain lesions, present in advanced atherosclerosis, share pathological hallmarks with peripheral vascular lesions, such as increased inflammation and oxidative stress. Physical activity reduces these peripheral risk factors, but its cerebrovascular effect is less documented, especially by non‐invasive imaging. Through a combination of in vivo and post‐mortem techniques, we aimed to characterize vascular brain damage in old ApoE−/− mice fed a high‐cholesterol (HC) diet with dietary controlled intake. We then sought to determine the beneficial effects of exercise training on oxidative stress and inflammation in the brain as a treatment option in an ageing atherosclerosis mouse model. Using in vivo magnetic resonance imaging (MRI) and biological markers of oxidative stress and inflammation, we evaluated the occurrence of vascular abnormalities in the brain of HC‐diet fed ApoE−/− mice >70 weeks old, its association with local and systemic oxidative stress and inflammation, and whether both can be modulated by exercise. Exercise training significantly reduced both MRI‐detected abnormalities (present in 71% of untrained vs. 14% of trained mice) and oxidative stress (lipid peroxidation, 9.1 ± 1.4 vs. 5.2 ± 0.9 μmol mg−1; P |
doi_str_mv | 10.1113/JP271903 |
format | Article |
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Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress.
Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation.
In this study, exercise training reduced magnetic resonance imaging‐detected abnormalities, insulin resistance and markers of oxidative stress and inflammation in old ApoE−/− mice.
Our results demonstrate the protective effect of exercise on neurovascular damage in the ageing brain of ApoE−/− mice.
Vascular brain lesions, present in advanced atherosclerosis, share pathological hallmarks with peripheral vascular lesions, such as increased inflammation and oxidative stress. Physical activity reduces these peripheral risk factors, but its cerebrovascular effect is less documented, especially by non‐invasive imaging. Through a combination of in vivo and post‐mortem techniques, we aimed to characterize vascular brain damage in old ApoE−/− mice fed a high‐cholesterol (HC) diet with dietary controlled intake. We then sought to determine the beneficial effects of exercise training on oxidative stress and inflammation in the brain as a treatment option in an ageing atherosclerosis mouse model. Using in vivo magnetic resonance imaging (MRI) and biological markers of oxidative stress and inflammation, we evaluated the occurrence of vascular abnormalities in the brain of HC‐diet fed ApoE−/− mice >70 weeks old, its association with local and systemic oxidative stress and inflammation, and whether both can be modulated by exercise. Exercise training significantly reduced both MRI‐detected abnormalities (present in 71% of untrained vs. 14% of trained mice) and oxidative stress (lipid peroxidation, 9.1 ± 1.4 vs. 5.2 ± 0.9 μmol mg−1; P < 0.01) and inflammation (interleukin‐1β, 226.8 ± 27.1 vs. 182.5 ± 21.5 pg mg−1; P < 0.05) in the brain, and the mortality rate. Exercise also decreased peripheral insulin resistance, oxidative stress and inflammation, but significant associations were seen only within brain markers. Highly localized vascular brain damage is a frequent finding in this ageing atherosclerosis model, and exercise is able to reduce this outcome and improve lifespan. In vivo MRI evaluated both the neurovascular damage and the protective effect of exercise.
Key points
Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress.
Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation.
In this study, exercise training reduced magnetic resonance imaging‐detected abnormalities, insulin resistance and markers of oxidative stress and inflammation in old ApoE−/− mice.
Our results demonstrate the protective effect of exercise on neurovascular damage in the ageing brain of ApoE−/− mice.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/JP271903</identifier><identifier>PMID: 27641234</identifier><identifier>CODEN: JPHYA7</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Aging - physiology ; Animals ; Aorta - diagnostic imaging ; Aorta - metabolism ; Apolipoproteins E - genetics ; Biomarkers - blood ; Biomarkers - metabolism ; Brain - diagnostic imaging ; Brain - metabolism ; Brain - pathology ; Cardiovascular ; Cardiovascular Conditions, Disorders and Treatments ; Catalase - metabolism ; Cholesterol - blood ; Diet, High-Fat ; Female ; Glutathione Peroxidase - metabolism ; Inflammation - blood ; Inflammation - metabolism ; Inflammation - pathology ; Inflammation - therapy ; Injury, Stress and Fatigue ; Interleukin-1beta - blood ; Interleukin-1beta - metabolism ; Life Sciences ; Magnetic Resonance Imaging ; Male ; Malondialdehyde - metabolism ; Mice, Inbred C57BL ; Mice, Knockout ; Nitrates - metabolism ; Nitrites - metabolism ; Oxidative Stress ; Physical Conditioning, Animal ; Research Paper ; Superoxide Dismutase - metabolism ; Tumor Necrosis Factor-alpha - blood ; Tumor Necrosis Factor-alpha - metabolism ; Vasculature</subject><ispartof>The Journal of physiology, 2016-12, Vol.594 (23), p.6969-6985</ispartof><rights>2016 The Authors. The Journal of Physiology © 2016 The Physiological Society</rights><rights>2016 The Authors. The Journal of Physiology © 2016 The Physiological Society.</rights><rights>Journal compilation © 2016 The Physiological Society</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4737-18bd8ada975e3f6f4027e8f87b47448e47dcc7267ae1ccc9218bcc512c48895a3</citedby><cites>FETCH-LOGICAL-c4737-18bd8ada975e3f6f4027e8f87b47448e47dcc7267ae1ccc9218bcc512c48895a3</cites><orcidid>0000-0001-8862-1431 ; 0000-0002-0146-0354 ; 0000-0001-5733-3672 ; 0000-0002-4177-741X ; 0000-0003-3378-5249 ; 0000-0002-1587-2253 ; 0000-0003-2057-061X ; 0000-0002-4742-5570 ; 0000-0002-9467-0317 ; 0000-0001-7921-1254</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/PMC5134731/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134731/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,1414,1430,27907,27908,45557,45558,46392,46816,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27641234$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01850360$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Chirico, Erica N.</creatorcontrib><creatorcontrib>Di Cataldo, Vanessa</creatorcontrib><creatorcontrib>Chauveau, Fabien</creatorcontrib><creatorcontrib>Geloën, Alain</creatorcontrib><creatorcontrib>Patsouris, David</creatorcontrib><creatorcontrib>Thézé, Benoît</creatorcontrib><creatorcontrib>Martin, Cyril</creatorcontrib><creatorcontrib>Vidal, Hubert</creatorcontrib><creatorcontrib>Rieusset, Jennifer</creatorcontrib><creatorcontrib>Pialoux, Vincent</creatorcontrib><creatorcontrib>Canet‐Soulas, Emmanuelle</creatorcontrib><title>Magnetic resonance imaging biomarkers of exercise‐induced improvement of oxidative stress and inflammation in the brain of old high‐fat‐fed ApoE−/− mice</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>Key points
Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress.
Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation.
In this study, exercise training reduced magnetic resonance imaging‐detected abnormalities, insulin resistance and markers of oxidative stress and inflammation in old ApoE−/− mice.
Our results demonstrate the protective effect of exercise on neurovascular damage in the ageing brain of ApoE−/− mice.
Vascular brain lesions, present in advanced atherosclerosis, share pathological hallmarks with peripheral vascular lesions, such as increased inflammation and oxidative stress. Physical activity reduces these peripheral risk factors, but its cerebrovascular effect is less documented, especially by non‐invasive imaging. Through a combination of in vivo and post‐mortem techniques, we aimed to characterize vascular brain damage in old ApoE−/− mice fed a high‐cholesterol (HC) diet with dietary controlled intake. We then sought to determine the beneficial effects of exercise training on oxidative stress and inflammation in the brain as a treatment option in an ageing atherosclerosis mouse model. Using in vivo magnetic resonance imaging (MRI) and biological markers of oxidative stress and inflammation, we evaluated the occurrence of vascular abnormalities in the brain of HC‐diet fed ApoE−/− mice >70 weeks old, its association with local and systemic oxidative stress and inflammation, and whether both can be modulated by exercise. Exercise training significantly reduced both MRI‐detected abnormalities (present in 71% of untrained vs. 14% of trained mice) and oxidative stress (lipid peroxidation, 9.1 ± 1.4 vs. 5.2 ± 0.9 μmol mg−1; P < 0.01) and inflammation (interleukin‐1β, 226.8 ± 27.1 vs. 182.5 ± 21.5 pg mg−1; P < 0.05) in the brain, and the mortality rate. Exercise also decreased peripheral insulin resistance, oxidative stress and inflammation, but significant associations were seen only within brain markers. Highly localized vascular brain damage is a frequent finding in this ageing atherosclerosis model, and exercise is able to reduce this outcome and improve lifespan. In vivo MRI evaluated both the neurovascular damage and the protective effect of exercise.
Key points
Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress.
Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation.
In this study, exercise training reduced magnetic resonance imaging‐detected abnormalities, insulin resistance and markers of oxidative stress and inflammation in old ApoE−/− mice.
Our results demonstrate the protective effect of exercise on neurovascular damage in the ageing brain of ApoE−/− mice.</description><subject>Aging - physiology</subject><subject>Animals</subject><subject>Aorta - diagnostic imaging</subject><subject>Aorta - metabolism</subject><subject>Apolipoproteins E - genetics</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - metabolism</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Cardiovascular</subject><subject>Cardiovascular Conditions, Disorders and Treatments</subject><subject>Catalase - metabolism</subject><subject>Cholesterol - blood</subject><subject>Diet, High-Fat</subject><subject>Female</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Inflammation - blood</subject><subject>Inflammation - metabolism</subject><subject>Inflammation - pathology</subject><subject>Inflammation - therapy</subject><subject>Injury, Stress and Fatigue</subject><subject>Interleukin-1beta - blood</subject><subject>Interleukin-1beta - metabolism</subject><subject>Life Sciences</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Malondialdehyde - metabolism</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Nitrates - metabolism</subject><subject>Nitrites - metabolism</subject><subject>Oxidative Stress</subject><subject>Physical Conditioning, Animal</subject><subject>Research Paper</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Tumor Necrosis Factor-alpha - blood</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Vasculature</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kstu1DAUQCMEotOCxBcgS2zaRVq_EicbpFFVKNUguihry3FuEpfEHuxkaHcsWSI-gU_rl-AwbYFKLPw-99jXuknyguBDQgg7OjungpSYPUoWhOdlKkTJHicLjClNmcjITrIbwiXGhOGyfJrsUJFzQhlfJD_fq9bCaDTyEJxVVgMyg2qNbVFl3KD8J_ABuQbBFXhtAtx8_W5sPWmoI7j2bgMD2HEm3JWp1Wg2gMIYbQEpGxnb9GoY4r6zcYHGDlDlVZzNEX2NOtN20dmoce6jdbl2JzfffhzFhgaj4VnypFF9gOe3417y8c3JxfFpuvrw9t3xcpVqLphISVHVhapVKTJgTd5wTAUUTSEqLjgvgItaa0FzoYBorUsaA7TOCNW8KMpMsb3k9da7nqoBah2z8qqXax__w19Lp4z898SaTrZuIzPC4gtIFBxsBd2DsNPlSs57mBQZZjnezOz-7WXefZ4gjHIwQUPfKwtuCpIUPKNZLgiO6KsH6KWbvI1f8ZviZVYw9keovQvBQ3P_AoLlXCTyrkgi-vLvRO_Bu6qIwOEW-GJ6uP6vSF6cnROKiWC_AP1Uy6g</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Chirico, Erica N.</creator><creator>Di Cataldo, Vanessa</creator><creator>Chauveau, Fabien</creator><creator>Geloën, Alain</creator><creator>Patsouris, David</creator><creator>Thézé, Benoît</creator><creator>Martin, Cyril</creator><creator>Vidal, Hubert</creator><creator>Rieusset, Jennifer</creator><creator>Pialoux, Vincent</creator><creator>Canet‐Soulas, Emmanuelle</creator><general>Wiley Subscription Services, Inc</general><general>Wiley</general><general>John Wiley and Sons Inc</general><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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8862-1431</orcidid><orcidid>https://orcid.org/0000-0002-0146-0354</orcidid><orcidid>https://orcid.org/0000-0001-5733-3672</orcidid><orcidid>https://orcid.org/0000-0002-4177-741X</orcidid><orcidid>https://orcid.org/0000-0003-3378-5249</orcidid><orcidid>https://orcid.org/0000-0002-1587-2253</orcidid><orcidid>https://orcid.org/0000-0003-2057-061X</orcidid><orcidid>https://orcid.org/0000-0002-4742-5570</orcidid><orcidid>https://orcid.org/0000-0002-9467-0317</orcidid><orcidid>https://orcid.org/0000-0001-7921-1254</orcidid></search><sort><creationdate>20161201</creationdate><title>Magnetic resonance imaging biomarkers of exercise‐induced improvement of oxidative stress and inflammation in the brain of old high‐fat‐fed ApoE−/− mice</title><author>Chirico, Erica N. ; Di Cataldo, Vanessa ; Chauveau, Fabien ; Geloën, Alain ; Patsouris, David ; Thézé, Benoît ; Martin, Cyril ; Vidal, Hubert ; Rieusset, Jennifer ; Pialoux, Vincent ; Canet‐Soulas, Emmanuelle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4737-18bd8ada975e3f6f4027e8f87b47448e47dcc7267ae1ccc9218bcc512c48895a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aging - physiology</topic><topic>Animals</topic><topic>Aorta - diagnostic imaging</topic><topic>Aorta - metabolism</topic><topic>Apolipoproteins E - genetics</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - metabolism</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Cardiovascular</topic><topic>Cardiovascular Conditions, Disorders and Treatments</topic><topic>Catalase - metabolism</topic><topic>Cholesterol - blood</topic><topic>Diet, High-Fat</topic><topic>Female</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Inflammation - blood</topic><topic>Inflammation - metabolism</topic><topic>Inflammation - pathology</topic><topic>Inflammation - therapy</topic><topic>Injury, Stress and Fatigue</topic><topic>Interleukin-1beta - blood</topic><topic>Interleukin-1beta - metabolism</topic><topic>Life Sciences</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Malondialdehyde - metabolism</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Nitrates - metabolism</topic><topic>Nitrites - metabolism</topic><topic>Oxidative Stress</topic><topic>Physical Conditioning, Animal</topic><topic>Research Paper</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Tumor Necrosis Factor-alpha - blood</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Vasculature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chirico, Erica N.</creatorcontrib><creatorcontrib>Di Cataldo, Vanessa</creatorcontrib><creatorcontrib>Chauveau, Fabien</creatorcontrib><creatorcontrib>Geloën, Alain</creatorcontrib><creatorcontrib>Patsouris, David</creatorcontrib><creatorcontrib>Thézé, Benoît</creatorcontrib><creatorcontrib>Martin, Cyril</creatorcontrib><creatorcontrib>Vidal, Hubert</creatorcontrib><creatorcontrib>Rieusset, Jennifer</creatorcontrib><creatorcontrib>Pialoux, Vincent</creatorcontrib><creatorcontrib>Canet‐Soulas, Emmanuelle</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chirico, Erica N.</au><au>Di Cataldo, Vanessa</au><au>Chauveau, Fabien</au><au>Geloën, Alain</au><au>Patsouris, David</au><au>Thézé, Benoît</au><au>Martin, Cyril</au><au>Vidal, Hubert</au><au>Rieusset, Jennifer</au><au>Pialoux, Vincent</au><au>Canet‐Soulas, Emmanuelle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnetic resonance imaging biomarkers of exercise‐induced improvement of oxidative stress and inflammation in the brain of old high‐fat‐fed ApoE−/− mice</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>594</volume><issue>23</issue><spage>6969</spage><epage>6985</epage><pages>6969-6985</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><coden>JPHYA7</coden><abstract>Key points
Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress.
Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation.
In this study, exercise training reduced magnetic resonance imaging‐detected abnormalities, insulin resistance and markers of oxidative stress and inflammation in old ApoE−/− mice.
Our results demonstrate the protective effect of exercise on neurovascular damage in the ageing brain of ApoE−/− mice.
Vascular brain lesions, present in advanced atherosclerosis, share pathological hallmarks with peripheral vascular lesions, such as increased inflammation and oxidative stress. Physical activity reduces these peripheral risk factors, but its cerebrovascular effect is less documented, especially by non‐invasive imaging. Through a combination of in vivo and post‐mortem techniques, we aimed to characterize vascular brain damage in old ApoE−/− mice fed a high‐cholesterol (HC) diet with dietary controlled intake. We then sought to determine the beneficial effects of exercise training on oxidative stress and inflammation in the brain as a treatment option in an ageing atherosclerosis mouse model. Using in vivo magnetic resonance imaging (MRI) and biological markers of oxidative stress and inflammation, we evaluated the occurrence of vascular abnormalities in the brain of HC‐diet fed ApoE−/− mice >70 weeks old, its association with local and systemic oxidative stress and inflammation, and whether both can be modulated by exercise. Exercise training significantly reduced both MRI‐detected abnormalities (present in 71% of untrained vs. 14% of trained mice) and oxidative stress (lipid peroxidation, 9.1 ± 1.4 vs. 5.2 ± 0.9 μmol mg−1; P < 0.01) and inflammation (interleukin‐1β, 226.8 ± 27.1 vs. 182.5 ± 21.5 pg mg−1; P < 0.05) in the brain, and the mortality rate. Exercise also decreased peripheral insulin resistance, oxidative stress and inflammation, but significant associations were seen only within brain markers. Highly localized vascular brain damage is a frequent finding in this ageing atherosclerosis model, and exercise is able to reduce this outcome and improve lifespan. In vivo MRI evaluated both the neurovascular damage and the protective effect of exercise.
Key points
Vascular brain lesions and atherosclerosis are two similar conditions that are characterized by increased inflammation and oxidative stress.
Non‐invasive imaging in a murine model of atherosclerosis showed vascular brain damage and peripheral inflammation.
In this study, exercise training reduced magnetic resonance imaging‐detected abnormalities, insulin resistance and markers of oxidative stress and inflammation in old ApoE−/− mice.
Our results demonstrate the protective effect of exercise on neurovascular damage in the ageing brain of ApoE−/− mice.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27641234</pmid><doi>10.1113/JP271903</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0001-8862-1431</orcidid><orcidid>https://orcid.org/0000-0002-0146-0354</orcidid><orcidid>https://orcid.org/0000-0001-5733-3672</orcidid><orcidid>https://orcid.org/0000-0002-4177-741X</orcidid><orcidid>https://orcid.org/0000-0003-3378-5249</orcidid><orcidid>https://orcid.org/0000-0002-1587-2253</orcidid><orcidid>https://orcid.org/0000-0003-2057-061X</orcidid><orcidid>https://orcid.org/0000-0002-4742-5570</orcidid><orcidid>https://orcid.org/0000-0002-9467-0317</orcidid><orcidid>https://orcid.org/0000-0001-7921-1254</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aging - physiology Animals Aorta - diagnostic imaging Aorta - metabolism Apolipoproteins E - genetics Biomarkers - blood Biomarkers - metabolism Brain - diagnostic imaging Brain - metabolism Brain - pathology Cardiovascular Cardiovascular Conditions, Disorders and Treatments Catalase - metabolism Cholesterol - blood Diet, High-Fat Female Glutathione Peroxidase - metabolism Inflammation - blood Inflammation - metabolism Inflammation - pathology Inflammation - therapy Injury, Stress and Fatigue Interleukin-1beta - blood Interleukin-1beta - metabolism Life Sciences Magnetic Resonance Imaging Male Malondialdehyde - metabolism Mice, Inbred C57BL Mice, Knockout Nitrates - metabolism Nitrites - metabolism Oxidative Stress Physical Conditioning, Animal Research Paper Superoxide Dismutase - metabolism Tumor Necrosis Factor-alpha - blood Tumor Necrosis Factor-alpha - metabolism Vasculature |
title | Magnetic resonance imaging biomarkers of exercise‐induced improvement of oxidative stress and inflammation in the brain of old high‐fat‐fed ApoE−/− mice |
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