Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents
Introduction: Obesity levels in the United States have significantly increased in the last forty years. Lifestyle and pharmacological treatments have been largely ineffective in treating obesity for most people. Both Resistant Starch (RS) and Dietary Sodium Butyrate (SB) are bioactivties which have...
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ndltd-LSU-oai-etd.lsu.edu-etd-10102010-1645352013-01-07T22:52:57Z Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents Vidrine, Kirk Adam Human Ecology Introduction: Obesity levels in the United States have significantly increased in the last forty years. Lifestyle and pharmacological treatments have been largely ineffective in treating obesity for most people. Both Resistant Starch (RS) and Dietary Sodium Butyrate (SB) are bioactivties which have shown the ability to decrease body fat levels of rodents without increasing physical activity or decreasing energy intake. Glucagon-like peptide 1 (GLP-1) and peptide YY (PYY) are gut hormones that may be involved in increased energy expenditure at a cellular level with dietary RS and SB. Objective: To discern if SB and RS both work through the increase of plasma GLP-1 and PYY. Also to see if a combination of RS and SB would lead to an increased or even an additive effect on the reduction of body fat levels in rodents. Methods: 60 Sprague Dawley rats were fed isocaloric diets of either control, SB, RS or a combination of RS and SB for 60 days. Measurements included food intake, body weight, abdominal fat, plasma PYY and GLP-1, and gastrointestinal tract weights. Results: There was no difference in caloric consumptions between any groups. According to factorial results, SB and RS both lowered abdominal fat. While the combination of RS and SB showed the lowest levels of abdominal body fat levels by t tests compared to control, there was not an additive effect of SB and RS. GLP-1 and PYY levels were not increased in the SB fed group. Conclusions: SB effects on body fat reduction are not associated with increased plasma GLP-1 and PYY levels as found in RS fed rodents. The combination of SB and RS have a greater effect on body fat than either alone, but the lack of an additive effect suggests a saturation level in a cellular mechanism by which both RS and SB may increase energy expenditure. Keenan, Michael Marks, Loren Finley, John LSU 2010-10-27 text application/pdf http://etd.lsu.edu/docs/available/etd-10102010-164535/ http://etd.lsu.edu/docs/available/etd-10102010-164535/ en unrestricted I hereby certify that, if appropriate, I have obtained and attached herein a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to LSU or its agents the non-exclusive license to archive and make accessible, under the conditions specified below and in appropriate University policies, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
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Human Ecology Vidrine, Kirk Adam Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents |
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Introduction: Obesity levels in the United States have significantly increased in the last forty years. Lifestyle and pharmacological treatments have been largely ineffective in treating obesity for most people. Both Resistant Starch (RS) and Dietary Sodium Butyrate (SB) are bioactivties which have shown the ability to decrease body fat levels of rodents without increasing physical activity or decreasing energy intake. Glucagon-like peptide 1 (GLP-1) and peptide YY (PYY) are gut hormones that may be involved in increased energy expenditure at a cellular level with dietary RS and SB. Objective: To discern if SB and RS both work through the increase of plasma GLP-1 and PYY. Also to see if a combination of RS and SB would lead to an increased or even an additive effect on the reduction of body fat levels in rodents. Methods: 60 Sprague Dawley rats were fed isocaloric diets of either control, SB, RS or a combination of RS and SB for 60 days. Measurements included food intake, body weight, abdominal fat, plasma PYY and GLP-1, and gastrointestinal tract weights. Results: There was no difference in caloric consumptions between any groups. According to factorial results, SB and RS both lowered abdominal fat. While the combination of RS and SB showed the lowest levels of abdominal body fat levels by t tests compared to control, there was not an additive effect of SB and RS. GLP-1 and PYY levels were not increased in the SB fed group. Conclusions: SB effects on body fat reduction are not associated with increased plasma GLP-1 and PYY levels as found in RS fed rodents. The combination of SB and RS have a greater effect on body fat than either alone, but the lack of an additive effect suggests a saturation level in a cellular mechanism by which both RS and SB may increase energy expenditure. |
author2 |
Keenan, Michael |
author_facet |
Keenan, Michael Vidrine, Kirk Adam |
author |
Vidrine, Kirk Adam |
author_sort |
Vidrine, Kirk Adam |
title |
Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents |
title_short |
Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents |
title_full |
Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents |
title_fullStr |
Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents |
title_full_unstemmed |
Resistant Starch and Sodium Butyrate Reduce Body Fat in Rodents |
title_sort |
resistant starch and sodium butyrate reduce body fat in rodents |
publisher |
LSU |
publishDate |
2010 |
url |
http://etd.lsu.edu/docs/available/etd-10102010-164535/ |
work_keys_str_mv |
AT vidrinekirkadam resistantstarchandsodiumbutyratereducebodyfatinrodents |
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