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
Hauptverfasser: 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
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container_end_page 6985
container_issue 23
container_start_page 6969
container_title The Journal of physiology
container_volume 594
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
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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 &gt;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 &lt; 0.01) and inflammation (interleukin‐1β, 226.8 ± 27.1 vs. 182.5 ± 21.5 pg mg−1; P &lt; 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. 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The Journal of Physiology © 2016 The Physiological Society</rights><rights>2016 The Authors. 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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 &gt;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 &lt; 0.01) and inflammation (interleukin‐1β, 226.8 ± 27.1 vs. 182.5 ± 21.5 pg mg−1; P &lt; 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 &amp; 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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 &gt;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 &lt; 0.01) and inflammation (interleukin‐1β, 226.8 ± 27.1 vs. 182.5 ± 21.5 pg mg−1; P &lt; 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. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; PubMed Central
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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