Diacylglycerols affect substrate oxidation and appetite in humans
Meals rich in diacylglycerols (DGs) instead of triacylglycerols (TGs) show beneficial effects on lipid metabolism and energy balance. These effects are probably attributable to differences in DG and TG metabolism, especially postprandial fat oxidation. We assessed the effects of partial replacement...
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Veröffentlicht in: | The American journal of clinical nutrition 2003-05, Vol.77 (5), p.1133-1139 |
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description | Meals rich in diacylglycerols (DGs) instead of triacylglycerols (TGs) show beneficial effects on lipid metabolism and energy balance. These effects are probably attributable to differences in DG and TG metabolism, especially postprandial fat oxidation.
We assessed the effects of partial replacement of TGs with DGs on substrate oxidation, energy expenditure (EE), relevant blood variables, and appetite.
Twelve healthy, dietarily unrestrained women participated in a single-blind, placebo-controlled, randomized trial with crossover design. For 3 d before and throughout a 36-h stay in a respiration chamber, subjects were fed energy-maintenance amounts of a diet consisting of 55% of energy from carbohydrate, 15% from protein, and 30% from fat. In the respiration chamber, 40% of the fat was consumed as DG-rich (80% DGs) oil or as TG-based control oil with a similar fatty acid profile.
Fat oxidation was significantly higher with DG treatment than with TG treatment. Appetite profiles during day 1 (24 h) did not differ significantly between the DG and TG treatments; however, feelings of hunger, appetite, estimated prospective food intake, and desire to eat were all significantly lower on day 2 (12 h) with DG treatment. Mean plasma beta-hydroxybutyrate tended to be higher with DG treatment, and the difference between the 2 treatments was significant at 1130 on day 2. Plasma lipid concentrations and resting and 24-h EE did not differ significantly between the 2 treatments.
Consumption of DGs in place of TGs does not alter EE but produces metabolic effects, particularly increases in fat oxidation, which may be associated with improved appetite control and energy balance. |
doi_str_mv | 10.1093/ajcn/77.5.1133 |
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We assessed the effects of partial replacement of TGs with DGs on substrate oxidation, energy expenditure (EE), relevant blood variables, and appetite.
Twelve healthy, dietarily unrestrained women participated in a single-blind, placebo-controlled, randomized trial with crossover design. For 3 d before and throughout a 36-h stay in a respiration chamber, subjects were fed energy-maintenance amounts of a diet consisting of 55% of energy from carbohydrate, 15% from protein, and 30% from fat. In the respiration chamber, 40% of the fat was consumed as DG-rich (80% DGs) oil or as TG-based control oil with a similar fatty acid profile.
Fat oxidation was significantly higher with DG treatment than with TG treatment. Appetite profiles during day 1 (24 h) did not differ significantly between the DG and TG treatments; however, feelings of hunger, appetite, estimated prospective food intake, and desire to eat were all significantly lower on day 2 (12 h) with DG treatment. Mean plasma beta-hydroxybutyrate tended to be higher with DG treatment, and the difference between the 2 treatments was significant at 1130 on day 2. Plasma lipid concentrations and resting and 24-h EE did not differ significantly between the 2 treatments.
Consumption of DGs in place of TGs does not alter EE but produces metabolic effects, particularly increases in fat oxidation, which may be associated with improved appetite control and energy balance.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.1093/ajcn/77.5.1133</identifier><identifier>PMID: 12716663</identifier><identifier>CODEN: AJCNAC</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Clinical Nutrition</publisher><subject>3-Hydroxybutyric Acid - blood ; Acids ; Adult ; Appetite - drug effects ; Biological and medical sciences ; Calorimetry, Indirect ; Carbohydrate Metabolism ; Cross-Over Studies ; Diglycerides - metabolism ; Diglycerides - pharmacology ; Energy Metabolism - drug effects ; Fats - metabolism ; Feeding. Feeding behavior ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Oxidation ; Oxidation-Reduction ; Proteins - metabolism ; Single-Blind Method ; Surveys and Questionnaires ; Triglycerides - metabolism ; Triglycerides - pharmacology ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>The American journal of clinical nutrition, 2003-05, Vol.77 (5), p.1133-1139</ispartof><rights>2003 INIST-CNRS</rights><rights>Copyright American Society for Clinical Nutrition, Inc. May 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-1b9728d7513c40b3bc684e60ca78d2a0e9f2adb96d3ebb54abcfadb924b73bb3</citedby><cites>FETCH-LOGICAL-c454t-1b9728d7513c40b3bc684e60ca78d2a0e9f2adb96d3ebb54abcfadb924b73bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14736267$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12716663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KAMPHUIS, Marleen M. J. W</creatorcontrib><creatorcontrib>MELA, David J</creatorcontrib><creatorcontrib>WESTERTERP-PLANTENGA, Margriet S</creatorcontrib><title>Diacylglycerols affect substrate oxidation and appetite in humans</title><title>The American journal of clinical nutrition</title><addtitle>Am J Clin Nutr</addtitle><description>Meals rich in diacylglycerols (DGs) instead of triacylglycerols (TGs) show beneficial effects on lipid metabolism and energy balance. These effects are probably attributable to differences in DG and TG metabolism, especially postprandial fat oxidation.
We assessed the effects of partial replacement of TGs with DGs on substrate oxidation, energy expenditure (EE), relevant blood variables, and appetite.
Twelve healthy, dietarily unrestrained women participated in a single-blind, placebo-controlled, randomized trial with crossover design. For 3 d before and throughout a 36-h stay in a respiration chamber, subjects were fed energy-maintenance amounts of a diet consisting of 55% of energy from carbohydrate, 15% from protein, and 30% from fat. In the respiration chamber, 40% of the fat was consumed as DG-rich (80% DGs) oil or as TG-based control oil with a similar fatty acid profile.
Fat oxidation was significantly higher with DG treatment than with TG treatment. Appetite profiles during day 1 (24 h) did not differ significantly between the DG and TG treatments; however, feelings of hunger, appetite, estimated prospective food intake, and desire to eat were all significantly lower on day 2 (12 h) with DG treatment. Mean plasma beta-hydroxybutyrate tended to be higher with DG treatment, and the difference between the 2 treatments was significant at 1130 on day 2. Plasma lipid concentrations and resting and 24-h EE did not differ significantly between the 2 treatments.
Consumption of DGs in place of TGs does not alter EE but produces metabolic effects, particularly increases in fat oxidation, which may be associated with improved appetite control and energy balance.</description><subject>3-Hydroxybutyric Acid - blood</subject><subject>Acids</subject><subject>Adult</subject><subject>Appetite - drug effects</subject><subject>Biological and medical sciences</subject><subject>Calorimetry, Indirect</subject><subject>Carbohydrate Metabolism</subject><subject>Cross-Over Studies</subject><subject>Diglycerides - metabolism</subject><subject>Diglycerides - pharmacology</subject><subject>Energy Metabolism - drug effects</subject><subject>Fats - metabolism</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Proteins - metabolism</subject><subject>Single-Blind Method</subject><subject>Surveys and Questionnaires</subject><subject>Triglycerides - metabolism</subject><subject>Triglycerides - pharmacology</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE1Lw0AQhhdRbK1ePUoQ9JZ0dyfZTY6lfkLBS-_L7GajKfmouwnYf29iAwVPwwzPvMw8hNwyGjGawRJ3pllKGSURYwBnZM4ySEPgVJ6TOaWUhxkTyYxceb-jlPE4FZdkxrhkQgiYk9VTieZQfVYHY11b-QCLwpou8L32ncPOBu1PmWNXtk2ATR7gfm-7chiXTfDV19j4a3JRYOXtzVQXZPvyvF2_hZuP1_f1ahOaOIm7kOlM8jSXCQMTUw3aiDS2ghqUac6R2qzgmOtM5GC1TmLUphh7HmsJWsOCPB5j96797q3vVF16Y6sKG9v2Xkng8PfTgtz_A3dt75rhNDUQGfCMwgBFR8i41ntnC7V3ZY3uoBhVo1g1ilVSqkSNYoeFuym117XNT_hkcgAeJgC9wapw2JjSn7hYguBCwi8jWoHK</recordid><startdate>20030501</startdate><enddate>20030501</enddate><creator>KAMPHUIS, Marleen M. J. W</creator><creator>MELA, David J</creator><creator>WESTERTERP-PLANTENGA, Margriet S</creator><general>American Society for Clinical Nutrition</general><general>American Society for Clinical Nutrition, Inc</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>7QP</scope><scope>7T7</scope><scope>7TS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20030501</creationdate><title>Diacylglycerols affect substrate oxidation and appetite in humans</title><author>KAMPHUIS, Marleen M. J. W ; MELA, David J ; WESTERTERP-PLANTENGA, Margriet S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-1b9728d7513c40b3bc684e60ca78d2a0e9f2adb96d3ebb54abcfadb924b73bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>3-Hydroxybutyric Acid - blood</topic><topic>Acids</topic><topic>Adult</topic><topic>Appetite - drug effects</topic><topic>Biological and medical sciences</topic><topic>Calorimetry, Indirect</topic><topic>Carbohydrate Metabolism</topic><topic>Cross-Over Studies</topic><topic>Diglycerides - metabolism</topic><topic>Diglycerides - pharmacology</topic><topic>Energy Metabolism - drug effects</topic><topic>Fats - metabolism</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Oxidation</topic><topic>Oxidation-Reduction</topic><topic>Proteins - metabolism</topic><topic>Single-Blind Method</topic><topic>Surveys and Questionnaires</topic><topic>Triglycerides - metabolism</topic><topic>Triglycerides - pharmacology</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KAMPHUIS, Marleen M. J. W</creatorcontrib><creatorcontrib>MELA, David J</creatorcontrib><creatorcontrib>WESTERTERP-PLANTENGA, Margriet S</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>Calcium & Calcified Tissue Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KAMPHUIS, Marleen M. J. W</au><au>MELA, David J</au><au>WESTERTERP-PLANTENGA, Margriet S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diacylglycerols affect substrate oxidation and appetite in humans</atitle><jtitle>The American journal of clinical nutrition</jtitle><addtitle>Am J Clin Nutr</addtitle><date>2003-05-01</date><risdate>2003</risdate><volume>77</volume><issue>5</issue><spage>1133</spage><epage>1139</epage><pages>1133-1139</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><coden>AJCNAC</coden><abstract>Meals rich in diacylglycerols (DGs) instead of triacylglycerols (TGs) show beneficial effects on lipid metabolism and energy balance. These effects are probably attributable to differences in DG and TG metabolism, especially postprandial fat oxidation.
We assessed the effects of partial replacement of TGs with DGs on substrate oxidation, energy expenditure (EE), relevant blood variables, and appetite.
Twelve healthy, dietarily unrestrained women participated in a single-blind, placebo-controlled, randomized trial with crossover design. For 3 d before and throughout a 36-h stay in a respiration chamber, subjects were fed energy-maintenance amounts of a diet consisting of 55% of energy from carbohydrate, 15% from protein, and 30% from fat. In the respiration chamber, 40% of the fat was consumed as DG-rich (80% DGs) oil or as TG-based control oil with a similar fatty acid profile.
Fat oxidation was significantly higher with DG treatment than with TG treatment. Appetite profiles during day 1 (24 h) did not differ significantly between the DG and TG treatments; however, feelings of hunger, appetite, estimated prospective food intake, and desire to eat were all significantly lower on day 2 (12 h) with DG treatment. Mean plasma beta-hydroxybutyrate tended to be higher with DG treatment, and the difference between the 2 treatments was significant at 1130 on day 2. Plasma lipid concentrations and resting and 24-h EE did not differ significantly between the 2 treatments.
Consumption of DGs in place of TGs does not alter EE but produces metabolic effects, particularly increases in fat oxidation, which may be associated with improved appetite control and energy balance.</abstract><cop>Bethesda, MD</cop><pub>American Society for Clinical Nutrition</pub><pmid>12716663</pmid><doi>10.1093/ajcn/77.5.1133</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3-Hydroxybutyric Acid - blood Acids Adult Appetite - drug effects Biological and medical sciences Calorimetry, Indirect Carbohydrate Metabolism Cross-Over Studies Diglycerides - metabolism Diglycerides - pharmacology Energy Metabolism - drug effects Fats - metabolism Feeding. Feeding behavior Female Fundamental and applied biological sciences. Psychology Humans Oxidation Oxidation-Reduction Proteins - metabolism Single-Blind Method Surveys and Questionnaires Triglycerides - metabolism Triglycerides - pharmacology Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Diacylglycerols affect substrate oxidation and appetite in humans |
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