Effect of carbohydrate ingestion on glycogen resynthesis in human liver and skeletal muscle, measured by (13)C MRS
This study investigated the effect of carbohydrate (CHO) ingestion on postexercise glycogen resynthesis, measured simultaneously in liver and muscle (n = 6) by (13)C magnetic resonance spectroscopy, and subsequent exercise capacity (n = 10). Subjects cycled at 70% maximal oxygen uptake for 83 +/- 8...
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description | This study investigated the effect of carbohydrate (CHO) ingestion on postexercise glycogen resynthesis, measured simultaneously in liver and muscle (n = 6) by (13)C magnetic resonance spectroscopy, and subsequent exercise capacity (n = 10). Subjects cycled at 70% maximal oxygen uptake for 83 +/- 8 min on six separate occasions. At the end of exercise, subjects ingested 1 g/kg body mass (BM) glucose, sucrose, or placebo (control). Resynthesis of glycogen over a 4-h period after treatment ingestion was measured on the first three occasions, and subsequent exercise capacity was measured on occasions four through six. No glycogen was resynthesized during the control trial. Liver glycogen resynthesis was evident after glucose (13 +/- 8 g) and sucrose (25 +/- 5 g) ingestion, both of which were different from control (P < 0.01). No significant differences in muscle glycogen resynthesis were found among trials. A relationship between the CHO load (g) and change in liver glycogen content (g) was evident after 30, 90, 150, and 210 min of recovery (r = 0.59-0. 79, P < 0.05). Furthermore, a modest relationship existed between change in liver glycogen content (g) and subsequent exercise capacity (r = 0.53, P < 0.05). However, no significant difference in mean exercise time was found (control: 35 +/- 5, glucose: 40 +/- 5, and sucrose: 46 +/- 6 min). Therefore, 1 g/kg BM glucose or sucrose is sufficient to initiate postexercise liver glycogen resynthesis, which contributes to subsequent exercise capacity, but not muscle glycogen resynthesis. |
doi_str_mv | 10.1152/ajpendo.2000.278.1.e65 |
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Subjects cycled at 70% maximal oxygen uptake for 83 +/- 8 min on six separate occasions. At the end of exercise, subjects ingested 1 g/kg body mass (BM) glucose, sucrose, or placebo (control). Resynthesis of glycogen over a 4-h period after treatment ingestion was measured on the first three occasions, and subsequent exercise capacity was measured on occasions four through six. No glycogen was resynthesized during the control trial. Liver glycogen resynthesis was evident after glucose (13 +/- 8 g) and sucrose (25 +/- 5 g) ingestion, both of which were different from control (P < 0.01). No significant differences in muscle glycogen resynthesis were found among trials. A relationship between the CHO load (g) and change in liver glycogen content (g) was evident after 30, 90, 150, and 210 min of recovery (r = 0.59-0. 79, P < 0.05). Furthermore, a modest relationship existed between change in liver glycogen content (g) and subsequent exercise capacity (r = 0.53, P < 0.05). However, no significant difference in mean exercise time was found (control: 35 +/- 5, glucose: 40 +/- 5, and sucrose: 46 +/- 6 min). Therefore, 1 g/kg BM glucose or sucrose is sufficient to initiate postexercise liver glycogen resynthesis, which contributes to subsequent exercise capacity, but not muscle glycogen resynthesis.</description><identifier>ISSN: 0193-1849</identifier><identifier>DOI: 10.1152/ajpendo.2000.278.1.e65</identifier><identifier>PMID: 10644538</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Blood - metabolism ; Carbon Isotopes ; Dietary Carbohydrates - metabolism ; Dietary Carbohydrates - pharmacology ; Glucose - pharmacology ; Glycogen - biosynthesis ; Glycogen - metabolism ; Humans ; Liver - anatomy & histology ; Liver - metabolism ; Magnetic Resonance Spectroscopy ; Male ; Muscle, Skeletal - anatomy & histology ; Muscle, Skeletal - metabolism ; Oxidation-Reduction ; Physical Endurance - physiology ; Reference Values ; Space life sciences ; Sucrose - pharmacology</subject><ispartof>American journal of physiology: endocrinology and metabolism, 2000-01, Vol.278 (1), p.E65-E75</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10644538$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Casey, A</creatorcontrib><creatorcontrib>Mann, R</creatorcontrib><creatorcontrib>Banister, K</creatorcontrib><creatorcontrib>Fox, J</creatorcontrib><creatorcontrib>Morris, P G</creatorcontrib><creatorcontrib>Macdonald, I A</creatorcontrib><creatorcontrib>Greenhaff, P L</creatorcontrib><title>Effect of carbohydrate ingestion on glycogen resynthesis in human liver and skeletal muscle, measured by (13)C MRS</title><title>American journal of physiology: endocrinology and metabolism</title><addtitle>Am J Physiol Endocrinol Metab</addtitle><description>This study investigated the effect of carbohydrate (CHO) ingestion on postexercise glycogen resynthesis, measured simultaneously in liver and muscle (n = 6) by (13)C magnetic resonance spectroscopy, and subsequent exercise capacity (n = 10). Subjects cycled at 70% maximal oxygen uptake for 83 +/- 8 min on six separate occasions. At the end of exercise, subjects ingested 1 g/kg body mass (BM) glucose, sucrose, or placebo (control). Resynthesis of glycogen over a 4-h period after treatment ingestion was measured on the first three occasions, and subsequent exercise capacity was measured on occasions four through six. No glycogen was resynthesized during the control trial. Liver glycogen resynthesis was evident after glucose (13 +/- 8 g) and sucrose (25 +/- 5 g) ingestion, both of which were different from control (P < 0.01). No significant differences in muscle glycogen resynthesis were found among trials. A relationship between the CHO load (g) and change in liver glycogen content (g) was evident after 30, 90, 150, and 210 min of recovery (r = 0.59-0. 79, P < 0.05). Furthermore, a modest relationship existed between change in liver glycogen content (g) and subsequent exercise capacity (r = 0.53, P < 0.05). However, no significant difference in mean exercise time was found (control: 35 +/- 5, glucose: 40 +/- 5, and sucrose: 46 +/- 6 min). Therefore, 1 g/kg BM glucose or sucrose is sufficient to initiate postexercise liver glycogen resynthesis, which contributes to subsequent exercise capacity, but not muscle glycogen resynthesis.</description><subject>Adult</subject><subject>Blood - metabolism</subject><subject>Carbon Isotopes</subject><subject>Dietary Carbohydrates - metabolism</subject><subject>Dietary Carbohydrates - pharmacology</subject><subject>Glucose - pharmacology</subject><subject>Glycogen - biosynthesis</subject><subject>Glycogen - metabolism</subject><subject>Humans</subject><subject>Liver - anatomy & histology</subject><subject>Liver - metabolism</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Male</subject><subject>Muscle, Skeletal - anatomy & histology</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Oxidation-Reduction</subject><subject>Physical Endurance - physiology</subject><subject>Reference Values</subject><subject>Space life sciences</subject><subject>Sucrose - pharmacology</subject><issn>0193-1849</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kF1LwzAYhXOhuDn9CyNXomBr3iRd00sZ8wMmgh_XJW3ebJ1tWpNW6L-34IQD5-I8HDiHkCWwGCDhd_rQoTNtzBljMU9VDDGukhMyZ5CJCJTMZuQ8hMMUp4nkZ2QGbCVlItSc-I21WPa0tbTUvmj3o_G6R1q5HYa-ah2dtKvHst2hox7D6Po9hipMBN0PjXa0rn7QU-0MDV9YY69r2gyhrPGWNqjD4NHQYqTXIG7W9OXt_YKcWl0HvDz6gnw-bD7WT9H29fF5fb-NOuC8j0Bn1pTaGqVKC6wQppQaNeMpJKnRAJmVDFPFmVI2U1JIroxNDTIFK0AhFuTqr7fz7fcwrcmbKpRY19phO4Q8ZSoDEMkELo_gUDRo8s5XjfZj_v-S-AUvpGrD</recordid><startdate>200001</startdate><enddate>200001</enddate><creator>Casey, A</creator><creator>Mann, R</creator><creator>Banister, K</creator><creator>Fox, J</creator><creator>Morris, P G</creator><creator>Macdonald, I A</creator><creator>Greenhaff, P L</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200001</creationdate><title>Effect of carbohydrate ingestion on glycogen resynthesis in human liver and skeletal muscle, measured by (13)C MRS</title><author>Casey, A ; Mann, R ; Banister, K ; Fox, J ; Morris, P G ; Macdonald, I A ; Greenhaff, P L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p122t-1a9fdcafd88cf10b3dc4aea027157da119f40e782088f9843428df7de08161e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Blood - metabolism</topic><topic>Carbon Isotopes</topic><topic>Dietary Carbohydrates - metabolism</topic><topic>Dietary Carbohydrates - pharmacology</topic><topic>Glucose - pharmacology</topic><topic>Glycogen - biosynthesis</topic><topic>Glycogen - metabolism</topic><topic>Humans</topic><topic>Liver - anatomy & histology</topic><topic>Liver - metabolism</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Male</topic><topic>Muscle, Skeletal - anatomy & histology</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Oxidation-Reduction</topic><topic>Physical Endurance - physiology</topic><topic>Reference Values</topic><topic>Space life sciences</topic><topic>Sucrose - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Casey, A</creatorcontrib><creatorcontrib>Mann, R</creatorcontrib><creatorcontrib>Banister, K</creatorcontrib><creatorcontrib>Fox, J</creatorcontrib><creatorcontrib>Morris, P G</creatorcontrib><creatorcontrib>Macdonald, I A</creatorcontrib><creatorcontrib>Greenhaff, P L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology: endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Casey, A</au><au>Mann, R</au><au>Banister, K</au><au>Fox, J</au><au>Morris, P G</au><au>Macdonald, I A</au><au>Greenhaff, P L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of carbohydrate ingestion on glycogen resynthesis in human liver and skeletal muscle, measured by (13)C MRS</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol Endocrinol Metab</addtitle><date>2000-01</date><risdate>2000</risdate><volume>278</volume><issue>1</issue><spage>E65</spage><epage>E75</epage><pages>E65-E75</pages><issn>0193-1849</issn><abstract>This study investigated the effect of carbohydrate (CHO) ingestion on postexercise glycogen resynthesis, measured simultaneously in liver and muscle (n = 6) by (13)C magnetic resonance spectroscopy, and subsequent exercise capacity (n = 10). Subjects cycled at 70% maximal oxygen uptake for 83 +/- 8 min on six separate occasions. At the end of exercise, subjects ingested 1 g/kg body mass (BM) glucose, sucrose, or placebo (control). Resynthesis of glycogen over a 4-h period after treatment ingestion was measured on the first three occasions, and subsequent exercise capacity was measured on occasions four through six. No glycogen was resynthesized during the control trial. Liver glycogen resynthesis was evident after glucose (13 +/- 8 g) and sucrose (25 +/- 5 g) ingestion, both of which were different from control (P < 0.01). No significant differences in muscle glycogen resynthesis were found among trials. A relationship between the CHO load (g) and change in liver glycogen content (g) was evident after 30, 90, 150, and 210 min of recovery (r = 0.59-0. 79, P < 0.05). Furthermore, a modest relationship existed between change in liver glycogen content (g) and subsequent exercise capacity (r = 0.53, P < 0.05). However, no significant difference in mean exercise time was found (control: 35 +/- 5, glucose: 40 +/- 5, and sucrose: 46 +/- 6 min). Therefore, 1 g/kg BM glucose or sucrose is sufficient to initiate postexercise liver glycogen resynthesis, which contributes to subsequent exercise capacity, but not muscle glycogen resynthesis.</abstract><cop>United States</cop><pmid>10644538</pmid><doi>10.1152/ajpendo.2000.278.1.e65</doi></addata></record> |
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subjects | Adult Blood - metabolism Carbon Isotopes Dietary Carbohydrates - metabolism Dietary Carbohydrates - pharmacology Glucose - pharmacology Glycogen - biosynthesis Glycogen - metabolism Humans Liver - anatomy & histology Liver - metabolism Magnetic Resonance Spectroscopy Male Muscle, Skeletal - anatomy & histology Muscle, Skeletal - metabolism Oxidation-Reduction Physical Endurance - physiology Reference Values Space life sciences Sucrose - pharmacology |
title | Effect of carbohydrate ingestion on glycogen resynthesis in human liver and skeletal muscle, measured by (13)C MRS |
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