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Level of glycogen stores and amount of ingested glucose regulate net carbohydrate storage by different mechanisms
The respective effects of the level of glycogen stores and the size of the glucose load on the pathways of carbohydrate (CHO) metabolism were compared over the 5-hour period following glucose ingestion in normal human subjects. For this purpose, labeling of the oral glucose load with [3-3H]- and [U1...
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Published in: | Metabolism, clinical and experimental clinical and experimental, 2003-01, Vol.52 (1), p.94-101 |
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description | The respective effects of the level of glycogen stores and the size of the glucose load on the pathways of carbohydrate (CHO) metabolism were compared over the 5-hour period following glucose ingestion in normal human subjects. For this purpose, labeling of the oral glucose load with [3-3H]- and [U14C] glucose was combined with indirect calorimetry. In group I, 75 g glucose was given to subjects who had either been “fed” with intravenous (IV) glucose or fasted for 13, 24, or 36 hours, or 4 days. In fed versus 4-day–fasted subjects, net CHO storage averaged approximately 15 versus 63 g/5 h (P |
doi_str_mv | 10.1053/meta.2003.50015 |
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For this purpose, labeling of the oral glucose load with [3-3H]- and [U14C] glucose was combined with indirect calorimetry. In group I, 75 g glucose was given to subjects who had either been “fed” with intravenous (IV) glucose or fasted for 13, 24, or 36 hours, or 4 days. In fed versus 4-day–fasted subjects, net CHO storage averaged approximately 15 versus 63 g/5 h (P <.001). About 83% of the increase in fasted subjects was due to suppression of glycogen breakdown, with only minimal stimulation of glycogen synthesis from oral glucose. Over the whole range of nutritional conditions tested, a strong positive correlation existed between basal CHO oxidation and glycogen breakdown occurring during the oral glucose tolerance test (OGTT), suggesting that the initial degree of repletion of hepatic glycogen stores is a major determinant of postprandial glycogen turnover. In group II, OGTTs with 33 and 100 g glucose were compared in 13-hour–fasted subjects. Net storage rose from approximately −6 to ~ 37 g/5 h (P <.001) solely because of an increase in glycogen synthesis with no inhibition of glycogen turnover. Overall, these results show that the initial dietary state and the size of the glucose load modulate postprandial net CHO accumulation by different mechanisms. Copyright 2003, Elsevier Science (USA). All rights reserved.</description><identifier>ISSN: 0026-0495</identifier><identifier>EISSN: 1532-8600</identifier><identifier>DOI: 10.1053/meta.2003.50015</identifier><identifier>PMID: 12524668</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Biological and medical sciences ; Blood Glucose - metabolism ; Calorimetry, Indirect ; Carbohydrate Metabolism ; Carbohydrates ; Female ; Fundamental and applied biological sciences. 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For this purpose, labeling of the oral glucose load with [3-3H]- and [U14C] glucose was combined with indirect calorimetry. In group I, 75 g glucose was given to subjects who had either been “fed” with intravenous (IV) glucose or fasted for 13, 24, or 36 hours, or 4 days. In fed versus 4-day–fasted subjects, net CHO storage averaged approximately 15 versus 63 g/5 h (P <.001). About 83% of the increase in fasted subjects was due to suppression of glycogen breakdown, with only minimal stimulation of glycogen synthesis from oral glucose. Over the whole range of nutritional conditions tested, a strong positive correlation existed between basal CHO oxidation and glycogen breakdown occurring during the oral glucose tolerance test (OGTT), suggesting that the initial degree of repletion of hepatic glycogen stores is a major determinant of postprandial glycogen turnover. In group II, OGTTs with 33 and 100 g glucose were compared in 13-hour–fasted subjects. Net storage rose from approximately −6 to ~ 37 g/5 h (P <.001) solely because of an increase in glycogen synthesis with no inhibition of glycogen turnover. Overall, these results show that the initial dietary state and the size of the glucose load modulate postprandial net CHO accumulation by different mechanisms. Copyright 2003, Elsevier Science (USA). All rights reserved.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - metabolism</subject><subject>Calorimetry, Indirect</subject><subject>Carbohydrate Metabolism</subject><subject>Carbohydrates</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose - pharmacology</subject><subject>Glucose Tolerance Test</subject><subject>Glycogen - biosynthesis</subject><subject>Glycogen - metabolism</subject><subject>Glycolysis - physiology</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Male</subject><subject>Metabolisms and neurohumoral controls</subject><subject>Nutritional Status - physiology</subject><subject>Oxidation-Reduction</subject><subject>Postprandial Period - physiology</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0026-0495</issn><issn>1532-8600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNp1kEFr3DAQRkVoSTZpz70VXZqbN5LGkq1jCW0aWOilPQtZGjkqtpVIdmD_fe3uQk49Dcy872N4hHzibM-ZhLsRZ7sXjMFeMsblBdlxCaJqFWPvyI4xoSpWa3lFrkv5wxhrmlZdkisupKiVanfk5YCvONAUaD8cXepxomVOGQu1k6d2TMs0b9c49Vhm9Cu2uFSQZuyXwc5IJ5yps7lLT0eft8WWtz3S7kh9DAEzrhUjuic7xTKWD-R9sEPBj-d5Q35___br_kd1-PnweP_1UDloYK40V6BD0yJKX3Ntg3LCA4BSGgK32HYNV0F6iS0HbXXNneOdbxsFgAAt3JDbU-9zTi_L-rwZY3E4DHbCtBTTCC1ZA2IF706gy6mUjME85zjafDScmc2y2SybzbL5Z3lNfD5XL92I_o0_a12BL2fAFmeHkO3kYnnjaiU4g61InzhcRbxGzKa4iJNDHzO62fgU__vEX9nLmkQ</recordid><startdate>200301</startdate><enddate>200301</enddate><creator>Féry, F.</creator><creator>Plat, L.</creator><creator>Balasse, E.O.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>200301</creationdate><title>Level of glycogen stores and amount of ingested glucose regulate net carbohydrate storage by different mechanisms</title><author>Féry, F. ; Plat, L. ; Balasse, E.O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-91639f78ee5d419af6c2d3336693f1ae8b716f5d5e8139a941cc1bd87633e3383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - metabolism</topic><topic>Calorimetry, Indirect</topic><topic>Carbohydrate Metabolism</topic><topic>Carbohydrates</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose - pharmacology</topic><topic>Glucose Tolerance Test</topic><topic>Glycogen - biosynthesis</topic><topic>Glycogen - metabolism</topic><topic>Glycolysis - physiology</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Male</topic><topic>Metabolisms and neurohumoral controls</topic><topic>Nutritional Status - physiology</topic><topic>Oxidation-Reduction</topic><topic>Postprandial Period - physiology</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Féry, F.</creatorcontrib><creatorcontrib>Plat, L.</creatorcontrib><creatorcontrib>Balasse, E.O.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Féry, F.</au><au>Plat, L.</au><au>Balasse, E.O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Level of glycogen stores and amount of ingested glucose regulate net carbohydrate storage by different mechanisms</atitle><jtitle>Metabolism, clinical and experimental</jtitle><addtitle>Metabolism</addtitle><date>2003-01</date><risdate>2003</risdate><volume>52</volume><issue>1</issue><spage>94</spage><epage>101</epage><pages>94-101</pages><issn>0026-0495</issn><eissn>1532-8600</eissn><abstract>The respective effects of the level of glycogen stores and the size of the glucose load on the pathways of carbohydrate (CHO) metabolism were compared over the 5-hour period following glucose ingestion in normal human subjects. 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Net storage rose from approximately −6 to ~ 37 g/5 h (P <.001) solely because of an increase in glycogen synthesis with no inhibition of glycogen turnover. Overall, these results show that the initial dietary state and the size of the glucose load modulate postprandial net CHO accumulation by different mechanisms. Copyright 2003, Elsevier Science (USA). All rights reserved.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12524668</pmid><doi>10.1053/meta.2003.50015</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Blood Glucose - metabolism Calorimetry, Indirect Carbohydrate Metabolism Carbohydrates Female Fundamental and applied biological sciences. Psychology Glucose - pharmacology Glucose Tolerance Test Glycogen - biosynthesis Glycogen - metabolism Glycolysis - physiology Humans Kinetics Male Metabolisms and neurohumoral controls Nutritional Status - physiology Oxidation-Reduction Postprandial Period - physiology Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Level of glycogen stores and amount of ingested glucose regulate net carbohydrate storage by different mechanisms |
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