Chitooligosaccharide induces mitochondrial biogenesis and increases exercise endurance through the activation of Sirt1 and AMPK in rats
By catabolizing glucose and lipids, mitochondria produce ATPs to meet energy demands. When the number and activity of mitochondria are not sufficient, the human body becomes easily fatigued due to the lack of ATP, thus the control of the quantity and function of mitochondria is important to optimize...
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creator | Jeong, Hyun Woo Cho, Si Young Kim, Shinae Shin, Eui Seok Kim, Jae Man Song, Min Jeong Park, Pil Joon Sohn, Jong Hee Park, Hyon Seo, Dae-Bang Kim, Wan Gi Lee, Sang-Jun |
description | By catabolizing glucose and lipids, mitochondria produce ATPs to meet energy demands. When the number and activity of mitochondria are not sufficient, the human body becomes easily fatigued due to the lack of ATP, thus the control of the quantity and function of mitochondria is important to optimize energy balance. By increasing mitochondrial capacity? it may be possible to enhance energy metabolism and improve exercise endurance. Here, through the screening of various functional food ingredients, we found that chitooligosaccharide (COS) is an effective inducer of mitochondrial biogenesis. In rodents, COS increased the mitochondrial content in skeletal muscle and enhanced exercise endurance. In cultured myocytes, the expression of major regulators of mitochondrial biogenesis and key components of mitochondrial electron transfer chain was increased upon COS treatment. COS-mediated induction of mitochondrial biogenesis was achieved in part by the activation of silent information regulator two ortholog 1 (Sirt1) and AMP-activated protein kinase (AMPK). Taken together, our data suggest that COS could act as an exercise mimetic by inducing mitochondrial biogenesis and enhancing exercise endurance through the activation of Sirt1 and AMPK. |
doi_str_mv | 10.1371/journal.pone.0040073 |
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When the number and activity of mitochondria are not sufficient, the human body becomes easily fatigued due to the lack of ATP, thus the control of the quantity and function of mitochondria is important to optimize energy balance. By increasing mitochondrial capacity? it may be possible to enhance energy metabolism and improve exercise endurance. Here, through the screening of various functional food ingredients, we found that chitooligosaccharide (COS) is an effective inducer of mitochondrial biogenesis. In rodents, COS increased the mitochondrial content in skeletal muscle and enhanced exercise endurance. In cultured myocytes, the expression of major regulators of mitochondrial biogenesis and key components of mitochondrial electron transfer chain was increased upon COS treatment. COS-mediated induction of mitochondrial biogenesis was achieved in part by the activation of silent information regulator two ortholog 1 (Sirt1) and AMP-activated protein kinase (AMPK). Taken together, our data suggest that COS could act as an exercise mimetic by inducing mitochondrial biogenesis and enhancing exercise endurance through the activation of Sirt1 and AMPK.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0040073</identifier><identifier>PMID: 22808092</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Activation ; AMP ; AMP-activated protein kinase ; Animals ; Biology ; Biosynthesis ; Cells, Cultured ; Chitosan - analogs & derivatives ; Chitosan - pharmacology ; Durability ; Electron transfer ; Endurance ; Energy balance ; Energy metabolism ; Energy Metabolism - drug effects ; Enzyme Activation - drug effects ; Female ; Functional foods ; Gene Expression - drug effects ; Glucose ; Humans ; Insulin resistance ; Kinases ; Lipid metabolism ; Lipids ; Medicine ; Metabolism ; Mitochondria ; Mitochondria, Muscle - drug effects ; Mitochondria, Muscle - enzymology ; Mitochondrial Turnover - drug effects ; Muscle Fibers, Skeletal - cytology ; Muscle Fibers, Skeletal - drug effects ; Muscle Fibers, Skeletal - enzymology ; Muscles ; Myocytes ; Physical Conditioning, Animal ; Physical Endurance - drug effects ; Physiological aspects ; Protein kinases ; Protein Kinases - genetics ; Protein Kinases - metabolism ; Rats ; Rats, Sprague-Dawley ; Regulators ; Rodents ; SIRT1 protein ; Sirtuin 1 - genetics ; Sirtuin 1 - metabolism ; Skeletal muscle</subject><ispartof>PloS one, 2012-07, Vol.7 (7), p.e40073</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Jeong et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Jeong et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-8af3dd88cf211804bdbd1d825c96dc5b95e16581f0abde25c7f7bcb64799c4bc3</citedby><cites>FETCH-LOGICAL-c692t-8af3dd88cf211804bdbd1d825c96dc5b95e16581f0abde25c7f7bcb64799c4bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394803/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394803/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22808092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jeong, Hyun Woo</creatorcontrib><creatorcontrib>Cho, Si Young</creatorcontrib><creatorcontrib>Kim, Shinae</creatorcontrib><creatorcontrib>Shin, Eui Seok</creatorcontrib><creatorcontrib>Kim, Jae Man</creatorcontrib><creatorcontrib>Song, Min Jeong</creatorcontrib><creatorcontrib>Park, Pil Joon</creatorcontrib><creatorcontrib>Sohn, Jong Hee</creatorcontrib><creatorcontrib>Park, Hyon</creatorcontrib><creatorcontrib>Seo, Dae-Bang</creatorcontrib><creatorcontrib>Kim, Wan Gi</creatorcontrib><creatorcontrib>Lee, Sang-Jun</creatorcontrib><title>Chitooligosaccharide induces mitochondrial biogenesis and increases exercise endurance through the activation of Sirt1 and AMPK in rats</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>By catabolizing glucose and lipids, mitochondria produce ATPs to meet energy demands. When the number and activity of mitochondria are not sufficient, the human body becomes easily fatigued due to the lack of ATP, thus the control of the quantity and function of mitochondria is important to optimize energy balance. By increasing mitochondrial capacity? it may be possible to enhance energy metabolism and improve exercise endurance. Here, through the screening of various functional food ingredients, we found that chitooligosaccharide (COS) is an effective inducer of mitochondrial biogenesis. In rodents, COS increased the mitochondrial content in skeletal muscle and enhanced exercise endurance. In cultured myocytes, the expression of major regulators of mitochondrial biogenesis and key components of mitochondrial electron transfer chain was increased upon COS treatment. COS-mediated induction of mitochondrial biogenesis was achieved in part by the activation of silent information regulator two ortholog 1 (Sirt1) and AMP-activated protein kinase (AMPK). Taken together, our data suggest that COS could act as an exercise mimetic by inducing mitochondrial biogenesis and enhancing exercise endurance through the activation of Sirt1 and AMPK.</description><subject>Activation</subject><subject>AMP</subject><subject>AMP-activated protein kinase</subject><subject>Animals</subject><subject>Biology</subject><subject>Biosynthesis</subject><subject>Cells, Cultured</subject><subject>Chitosan - analogs & derivatives</subject><subject>Chitosan - pharmacology</subject><subject>Durability</subject><subject>Electron transfer</subject><subject>Endurance</subject><subject>Energy balance</subject><subject>Energy metabolism</subject><subject>Energy Metabolism - drug effects</subject><subject>Enzyme Activation - drug effects</subject><subject>Female</subject><subject>Functional foods</subject><subject>Gene Expression - drug effects</subject><subject>Glucose</subject><subject>Humans</subject><subject>Insulin resistance</subject><subject>Kinases</subject><subject>Lipid metabolism</subject><subject>Lipids</subject><subject>Medicine</subject><subject>Metabolism</subject><subject>Mitochondria</subject><subject>Mitochondria, Muscle - drug effects</subject><subject>Mitochondria, Muscle - enzymology</subject><subject>Mitochondrial Turnover - drug effects</subject><subject>Muscle Fibers, Skeletal - cytology</subject><subject>Muscle Fibers, Skeletal - drug effects</subject><subject>Muscle Fibers, Skeletal - enzymology</subject><subject>Muscles</subject><subject>Myocytes</subject><subject>Physical Conditioning, Animal</subject><subject>Physical Endurance - drug effects</subject><subject>Physiological aspects</subject><subject>Protein kinases</subject><subject>Protein Kinases - genetics</subject><subject>Protein Kinases - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regulators</subject><subject>Rodents</subject><subject>SIRT1 protein</subject><subject>Sirtuin 1 - genetics</subject><subject>Sirtuin 1 - metabolism</subject><subject>Skeletal muscle</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12L1DAUhoso7rr6D0QLguDFjPlqm94sDIMfgysrrnobTj7aZug0Y5Iu6y_wb5vZ6S4zoCC9SDl53jeHl3Oy7DlGc0wr_HbtRj9AP9-6wcwRYghV9EF2imtKZiVB9OHB_0n2JIQ1QgXlZfk4OyGEI45qcpr9XnY2Otfb1gVQqgNvtcntoEdlQr5Jd6pzg_YW-lxa15rBBBtyGHSClDcQEmZujFc2mNwknYdBmTx23o1tl06Tg4r2GqJ1Q-6a_Mr6iG8NFp-_fEouuYcYnmaPGuiDeTadZ9n39---LT_OLi4_rJaLi5kqaxJnHBqqNeeqIRhzxKSWGmtOClWXWhWyLgwuC44bBFKbVK6aSipZsqquFZOKnmUv977b3gUxZRgEpqQoUogVScRqT2gHa7H1dgP-l3BgxW3B-VaAj1b1RnBGSiKh4ViVrEQAlDNcIalwVaXsZfI6n14b5cZoZYbooT8yPb4ZbCdady0orRlHNBm8mgy8-zmaEP_R8kS1kLqyQ-OSmdrYoMSCpVYwZYwnav4XKn3abKxKU9TYVD8SvDkSJCaam9jCGIJYXX39f_byxzH7-oDtDPSxC64fdxMSjkG2B5V3IXjT3CeHkdgtwV0aYrcEYlqCJHtxmPq96G7q6R--oQRD</recordid><startdate>20120711</startdate><enddate>20120711</enddate><creator>Jeong, Hyun Woo</creator><creator>Cho, Si Young</creator><creator>Kim, Shinae</creator><creator>Shin, Eui Seok</creator><creator>Kim, Jae Man</creator><creator>Song, Min Jeong</creator><creator>Park, Pil Joon</creator><creator>Sohn, Jong Hee</creator><creator>Park, Hyon</creator><creator>Seo, Dae-Bang</creator><creator>Kim, Wan Gi</creator><creator>Lee, Sang-Jun</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20120711</creationdate><title>Chitooligosaccharide induces mitochondrial biogenesis and increases exercise endurance through the activation of Sirt1 and AMPK in rats</title><author>Jeong, Hyun Woo ; Cho, Si Young ; Kim, Shinae ; Shin, Eui Seok ; Kim, Jae Man ; Song, Min Jeong ; Park, Pil Joon ; Sohn, Jong Hee ; Park, Hyon ; Seo, Dae-Bang ; Kim, Wan Gi ; Lee, Sang-Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-8af3dd88cf211804bdbd1d825c96dc5b95e16581f0abde25c7f7bcb64799c4bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Activation</topic><topic>AMP</topic><topic>AMP-activated protein kinase</topic><topic>Animals</topic><topic>Biology</topic><topic>Biosynthesis</topic><topic>Cells, Cultured</topic><topic>Chitosan - analogs & derivatives</topic><topic>Chitosan - pharmacology</topic><topic>Durability</topic><topic>Electron transfer</topic><topic>Endurance</topic><topic>Energy balance</topic><topic>Energy metabolism</topic><topic>Energy Metabolism - drug effects</topic><topic>Enzyme Activation - drug effects</topic><topic>Female</topic><topic>Functional foods</topic><topic>Gene Expression - drug effects</topic><topic>Glucose</topic><topic>Humans</topic><topic>Insulin resistance</topic><topic>Kinases</topic><topic>Lipid metabolism</topic><topic>Lipids</topic><topic>Medicine</topic><topic>Metabolism</topic><topic>Mitochondria</topic><topic>Mitochondria, Muscle - drug effects</topic><topic>Mitochondria, Muscle - enzymology</topic><topic>Mitochondrial Turnover - drug effects</topic><topic>Muscle Fibers, Skeletal - cytology</topic><topic>Muscle Fibers, Skeletal - drug effects</topic><topic>Muscle Fibers, Skeletal - enzymology</topic><topic>Muscles</topic><topic>Myocytes</topic><topic>Physical Conditioning, Animal</topic><topic>Physical Endurance - 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When the number and activity of mitochondria are not sufficient, the human body becomes easily fatigued due to the lack of ATP, thus the control of the quantity and function of mitochondria is important to optimize energy balance. By increasing mitochondrial capacity? it may be possible to enhance energy metabolism and improve exercise endurance. Here, through the screening of various functional food ingredients, we found that chitooligosaccharide (COS) is an effective inducer of mitochondrial biogenesis. In rodents, COS increased the mitochondrial content in skeletal muscle and enhanced exercise endurance. In cultured myocytes, the expression of major regulators of mitochondrial biogenesis and key components of mitochondrial electron transfer chain was increased upon COS treatment. COS-mediated induction of mitochondrial biogenesis was achieved in part by the activation of silent information regulator two ortholog 1 (Sirt1) and AMP-activated protein kinase (AMPK). Taken together, our data suggest that COS could act as an exercise mimetic by inducing mitochondrial biogenesis and enhancing exercise endurance through the activation of Sirt1 and AMPK.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22808092</pmid><doi>10.1371/journal.pone.0040073</doi><oa>free_for_read</oa></addata></record> |
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subjects | Activation AMP AMP-activated protein kinase Animals Biology Biosynthesis Cells, Cultured Chitosan - analogs & derivatives Chitosan - pharmacology Durability Electron transfer Endurance Energy balance Energy metabolism Energy Metabolism - drug effects Enzyme Activation - drug effects Female Functional foods Gene Expression - drug effects Glucose Humans Insulin resistance Kinases Lipid metabolism Lipids Medicine Metabolism Mitochondria Mitochondria, Muscle - drug effects Mitochondria, Muscle - enzymology Mitochondrial Turnover - drug effects Muscle Fibers, Skeletal - cytology Muscle Fibers, Skeletal - drug effects Muscle Fibers, Skeletal - enzymology Muscles Myocytes Physical Conditioning, Animal Physical Endurance - drug effects Physiological aspects Protein kinases Protein Kinases - genetics Protein Kinases - metabolism Rats Rats, Sprague-Dawley Regulators Rodents SIRT1 protein Sirtuin 1 - genetics Sirtuin 1 - metabolism Skeletal muscle |
title | Chitooligosaccharide induces mitochondrial biogenesis and increases exercise endurance through the activation of Sirt1 and AMPK in rats |
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