Time to run: Late rather than early exercise training in mice remodels the gut microbiome and reduces atherosclerosis development
The metabolic and inflammatory processes that are implicated in the development of cardiovascular diseases are under control of the biological clock. While skeletal muscle function exhibits circadian rhythms, it is unclear to what extent the beneficial health effects of exercise are restricted to un...
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creator | Schönke, Milena Ying, Zhixiong Kovynev, Artemiy In het Panhuis, Wietse Binnendijk, Anne van der Poel, Sabine Pronk, Amanda C. M. Streefland, Trea C. M. Hoekstra, Menno Kooijman, Sander Rensen, Patrick C. N. |
description | The metabolic and inflammatory processes that are implicated in the development of cardiovascular diseases are under control of the biological clock. While skeletal muscle function exhibits circadian rhythms, it is unclear to what extent the beneficial health effects of exercise are restricted to unique time windows. We aimed to study whether the timing of exercise training differentially modulates the development of atherosclerosis and elucidate underlying mechanisms. We endurance‐trained atherosclerosis‐prone female APOE*3‐Leiden.CETP mice fed a Western‐type diet, a well‐established human‐like model for cardiometabolic diseases, for 1 h five times a week for 4 weeks either in their early or in their late active phase on a treadmill. We monitored metabolic parameters, the development of atherosclerotic lesions in the aortic root and assessed the composition of the gut microbiota. Late, but not early, exercise training reduced fat mass by 19% and the size of early‐stage atherosclerotic lesions by as much as 29% compared to sedentary animals. No correlation between cholesterol exposure and lesion size was evident, as no differences in plasma lipid levels were observed, but circulating levels of the pro‐inflammatory markers ICAM‐1 and VCAM‐1 were reduced with late exercise. Strikingly, we observed a time‐of‐day‐dependent effect of exercise training on the composition of the gut microbiota as only late training increased the abundance of gut bacteria producing short‐chain fatty acids with proposed anti‐inflammatory properties. Together, these findings indicate that timing is a critical factor to the beneficial anti‐atherosclerotic effects of exercise with a great potential to further optimize training recommendations for patients. |
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M. ; Streefland, Trea C. M. ; Hoekstra, Menno ; Kooijman, Sander ; Rensen, Patrick C. N.</creator><creatorcontrib>Schönke, Milena ; Ying, Zhixiong ; Kovynev, Artemiy ; In het Panhuis, Wietse ; Binnendijk, Anne ; van der Poel, Sabine ; Pronk, Amanda C. M. ; Streefland, Trea C. M. ; Hoekstra, Menno ; Kooijman, Sander ; Rensen, Patrick C. N.</creatorcontrib><description>The metabolic and inflammatory processes that are implicated in the development of cardiovascular diseases are under control of the biological clock. While skeletal muscle function exhibits circadian rhythms, it is unclear to what extent the beneficial health effects of exercise are restricted to unique time windows. We aimed to study whether the timing of exercise training differentially modulates the development of atherosclerosis and elucidate underlying mechanisms. We endurance‐trained atherosclerosis‐prone female APOE*3‐Leiden.CETP mice fed a Western‐type diet, a well‐established human‐like model for cardiometabolic diseases, for 1 h five times a week for 4 weeks either in their early or in their late active phase on a treadmill. We monitored metabolic parameters, the development of atherosclerotic lesions in the aortic root and assessed the composition of the gut microbiota. Late, but not early, exercise training reduced fat mass by 19% and the size of early‐stage atherosclerotic lesions by as much as 29% compared to sedentary animals. No correlation between cholesterol exposure and lesion size was evident, as no differences in plasma lipid levels were observed, but circulating levels of the pro‐inflammatory markers ICAM‐1 and VCAM‐1 were reduced with late exercise. Strikingly, we observed a time‐of‐day‐dependent effect of exercise training on the composition of the gut microbiota as only late training increased the abundance of gut bacteria producing short‐chain fatty acids with proposed anti‐inflammatory properties. Together, these findings indicate that timing is a critical factor to the beneficial anti‐atherosclerotic effects of exercise with a great potential to further optimize training recommendations for patients.</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.202201304R</identifier><identifier>PMID: 36562708</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Apolipoprotein E3 ; atherosclerosis ; Atherosclerosis - metabolism ; Cholesterol ; circadian rhythms ; Diet, High-Fat ; exercise ; Fatty Acids, Volatile - pharmacology ; Female ; Gastrointestinal Microbiome ; gut microbiota ; Humans ; lipid metabolism ; Mice ; Mice, Inbred C57BL</subject><ispartof>The FASEB journal, 2023-01, Vol.37 (1), p.e22719-n/a</ispartof><rights>2022 The Authors. published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology.</rights><rights>2022 The Authors. 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Strikingly, we observed a time‐of‐day‐dependent effect of exercise training on the composition of the gut microbiota as only late training increased the abundance of gut bacteria producing short‐chain fatty acids with proposed anti‐inflammatory properties. Together, these findings indicate that timing is a critical factor to the beneficial anti‐atherosclerotic effects of exercise with a great potential to further optimize training recommendations for patients.</description><subject>Animals</subject><subject>Apolipoprotein E3</subject><subject>atherosclerosis</subject><subject>Atherosclerosis - metabolism</subject><subject>Cholesterol</subject><subject>circadian rhythms</subject><subject>Diet, High-Fat</subject><subject>exercise</subject><subject>Fatty Acids, Volatile - pharmacology</subject><subject>Female</subject><subject>Gastrointestinal Microbiome</subject><subject>gut microbiota</subject><subject>Humans</subject><subject>lipid metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp90E1PGzEQgGGromoC9Ngr8pHLpvY4_uIGUYFKkSq19LxydsfE0X4EexfIsf8ch0B768WWPI9eyUPIF85mnFn11W9mwAAYF2z-8wOZcilYoYxiR2TKjIVCKWEm5DilDWOMM64-kYlQUoFmZkr-3IUW6dDTOHYXdOkGpNENa4x0WLuOoovNjuIzxiqk7KILXejuaehoG6psse1rbFLWSO_HYf8a-1Xoc9R1dZ7XY4WJvib7VDX7MyRa4yM2_bbFbjglH71rEn5-u0_I7-tvd4vbYvnj5vvicllUQmtbADhALY2WFXg0Ky3BAnipLau0rSWYWiD3wgtUVknmjddGoXYSrbVzJU7I-aG7jf3DiGko25AqbBrXYT-mEnKccyEFz7Q40PyXlCL6chtD6-Ku5Kzcb730m_Lf1rM_e0uPqxbrv_p9zRnMD-ApNLj7f628_nUFAJpb8QKYbo4S</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Schönke, Milena</creator><creator>Ying, Zhixiong</creator><creator>Kovynev, Artemiy</creator><creator>In het Panhuis, Wietse</creator><creator>Binnendijk, Anne</creator><creator>van der Poel, Sabine</creator><creator>Pronk, Amanda C. 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N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time to run: Late rather than early exercise training in mice remodels the gut microbiome and reduces atherosclerosis development</atitle><jtitle>The FASEB journal</jtitle><addtitle>FASEB J</addtitle><date>2023-01</date><risdate>2023</risdate><volume>37</volume><issue>1</issue><spage>e22719</spage><epage>n/a</epage><pages>e22719-n/a</pages><issn>0892-6638</issn><eissn>1530-6860</eissn><abstract>The metabolic and inflammatory processes that are implicated in the development of cardiovascular diseases are under control of the biological clock. While skeletal muscle function exhibits circadian rhythms, it is unclear to what extent the beneficial health effects of exercise are restricted to unique time windows. We aimed to study whether the timing of exercise training differentially modulates the development of atherosclerosis and elucidate underlying mechanisms. 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subjects | Animals Apolipoprotein E3 atherosclerosis Atherosclerosis - metabolism Cholesterol circadian rhythms Diet, High-Fat exercise Fatty Acids, Volatile - pharmacology Female Gastrointestinal Microbiome gut microbiota Humans lipid metabolism Mice Mice, Inbred C57BL |
title | Time to run: Late rather than early exercise training in mice remodels the gut microbiome and reduces atherosclerosis development |
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