Resistant starch from high amylose maize (HAM‐RS2) reduces body fat and increases gut bacteria in ovariectomized (OVX) rats

Objective: Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with a prebiotic is a plausible strategy for improving the health of menopausal females. Design and Methods: Resistant starch type 2 f...

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Published inObesity (Silver Spring, Md.) Vol. 21; no. 5; pp. 981 - 984
Main Authors Keenan, Michael J., Janes, Marlene, Robert, Julina, Martin, Roy J., Raggio, Anne M., McCutcheon, Kathleen L., Pelkman, Christine, Tulley, Richard, Goita, M'Famara, Durham, Holiday A., Zhou, June, Senevirathne, Reshani N.
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.05.2013
Blackwell Publishing Ltd
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Abstract Objective: Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with a prebiotic is a plausible strategy for improving the health of menopausal females. Design and Methods: Resistant starch type 2 from high‐amylose maize (HAM‐RS2) was used as a prebiotic in rats in a 2 × 2 factorial study with two levels of HAM‐RS2 (0 or 29.7% of weight of diet) referred to as energy control (EC) and HAM‐RS2 diets, respectively; and two levels of surgery, ovariectomized (OVX) and sham. Results: In a 6‐week, postsurgery recovery period, OVX rats gained more body weight with consumption of a similar amount of food. Subsequently, consumption of HAM‐RS2 versus EC diets resulted in reduced abdominal fat in both OVX and sham rats; but when normalized for disemboweled body weight (body weight minus GI tract), there was no effect of surgery, only reduction with HAM‐RS2. Targeted bacterial populations were estimated that are known to ferment HAM‐RS2 or metabolize the products of that initial fermentation. OVX and sham rats demonstrated increased bacterial levels with dietary HAM‐RS2 for all bacteria. Additionally, culture techniques and qPCR provided similar results. Conclusion: This study shows that, as expected, OVX increases adiposity. However, contrary to previous effects seen in obese mice, this did not prevent fermentation of HAM‐RS2 and consequently, the fat gain associated with OVX was attenuated.
AbstractList Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with a prebiotic is a plausible strategy for improving the health of menopausal females. Resistant starch type 2 from high-amylose maize (HAM-RS2) was used as a prebiotic in rats in a 2 × 2 factorial study with two levels of HAM-RS2 (0 or 29.7% of weight of diet) referred to as energy control (EC) and HAM-RS2 diets, respectively; and two levels of surgery, ovariectomized (OVX) and sham. In a 6-week, postsurgery recovery period, OVX rats gained more body weight with consumption of a similar amount of food. Subsequently, consumption of HAM-RS2 versus EC diets resulted in reduced abdominal fat in both OVX and sham rats; but when normalized for disemboweled body weight (body weight minus GI tract), there was no effect of surgery, only reduction with HAM-RS2. Targeted bacterial populations were estimated that are known to ferment HAM-RS2 or metabolize the products of that initial fermentation. OVX and sham rats demonstrated increased bacterial levels with dietary HAMRS2 for all bacteria. Additionally, culture techniques and qPCR provided similar results. This study shows that, as expected, OVX increases adiposity. However, contrary to previous effects seen in obese mice, this did not prevent fermentation of HAM-RS2 and consequently, the fat gain associated with OVX was attenuated.
Objective: Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with a prebiotic is a plausible strategy for improving the health of menopausal females. Design and Methods: Resistant starch type 2 from high‐amylose maize (HAM‐RS2) was used as a prebiotic in rats in a 2 × 2 factorial study with two levels of HAM‐RS2 (0 or 29.7% of weight of diet) referred to as energy control (EC) and HAM‐RS2 diets, respectively; and two levels of surgery, ovariectomized (OVX) and sham. Results: In a 6‐week, postsurgery recovery period, OVX rats gained more body weight with consumption of a similar amount of food. Subsequently, consumption of HAM‐RS2 versus EC diets resulted in reduced abdominal fat in both OVX and sham rats; but when normalized for disemboweled body weight (body weight minus GI tract), there was no effect of surgery, only reduction with HAM‐RS2. Targeted bacterial populations were estimated that are known to ferment HAM‐RS2 or metabolize the products of that initial fermentation. OVX and sham rats demonstrated increased bacterial levels with dietary HAM‐RS2 for all bacteria. Additionally, culture techniques and qPCR provided similar results. Conclusion: This study shows that, as expected, OVX increases adiposity. However, contrary to previous effects seen in obese mice, this did not prevent fermentation of HAM‐RS2 and consequently, the fat gain associated with OVX was attenuated.
Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with a prebiotic is a plausible strategy for improving the health of menopausal females. Resistant starch type 2 from high-amylose maize (HAM-RS2) was used as a prebiotic in rats in a 2 × 2 factorial study with two levels of HAM-RS2 (0 or 29.7% of weight of diet) referred to as energy control (EC) and HAM-RS2 diets, respectively; and two levels of surgery, ovariectomized (OVX) and sham. In a 6-week, postsurgery recovery period, OVX rats gained more body weight with consumption of a similar amount of food. Subsequently, consumption of HAM-RS2 versus EC diets resulted in reduced abdominal fat in both OVX and sham rats; but when normalized for disemboweled body weight (body weight minus GI tract), there was no effect of surgery, only reduction with HAM-RS2. Targeted bacterial populations were estimated that are known to ferment HAM-RS2 or metabolize the products of that initial fermentation. OVX and sham rats demonstrated increased bacterial levels with dietary HAM-RS2 for all bacteria. Additionally, culture techniques and qPCR provided similar results. This study shows that, as expected, OVX increases adiposity. However, contrary to previous effects seen in obese mice, this did not prevent fermentation of HAM-RS2 and consequently, the fat gain associated with OVX was attenuated.
Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with a prebiotic is a plausible strategy for improving the health of menopausal females.OBJECTIVEObesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with a prebiotic is a plausible strategy for improving the health of menopausal females.Resistant starch type 2 from high-amylose maize (HAM-RS2) was used as a prebiotic in rats in a 2 × 2 factorial study with two levels of HAM-RS2 (0 or 29.7% of weight of diet) referred to as energy control (EC) and HAM-RS2 diets, respectively; and two levels of surgery, ovariectomized (OVX) and sham.DESIGN AND METHODSResistant starch type 2 from high-amylose maize (HAM-RS2) was used as a prebiotic in rats in a 2 × 2 factorial study with two levels of HAM-RS2 (0 or 29.7% of weight of diet) referred to as energy control (EC) and HAM-RS2 diets, respectively; and two levels of surgery, ovariectomized (OVX) and sham.In a 6-week, postsurgery recovery period, OVX rats gained more body weight with consumption of a similar amount of food. Subsequently, consumption of HAM-RS2 versus EC diets resulted in reduced abdominal fat in both OVX and sham rats; but when normalized for disemboweled body weight (body weight minus GI tract), there was no effect of surgery, only reduction with HAM-RS2. Targeted bacterial populations were estimated that are known to ferment HAM-RS2 or metabolize the products of that initial fermentation. OVX and sham rats demonstrated increased bacterial levels with dietary HAM-RS2 for all bacteria. Additionally, culture techniques and qPCR provided similar results.RESULTSIn a 6-week, postsurgery recovery period, OVX rats gained more body weight with consumption of a similar amount of food. Subsequently, consumption of HAM-RS2 versus EC diets resulted in reduced abdominal fat in both OVX and sham rats; but when normalized for disemboweled body weight (body weight minus GI tract), there was no effect of surgery, only reduction with HAM-RS2. Targeted bacterial populations were estimated that are known to ferment HAM-RS2 or metabolize the products of that initial fermentation. OVX and sham rats demonstrated increased bacterial levels with dietary HAM-RS2 for all bacteria. Additionally, culture techniques and qPCR provided similar results.This study shows that, as expected, OVX increases adiposity. However, contrary to previous effects seen in obese mice, this did not prevent fermentation of HAM-RS2 and consequently, the fat gain associated with OVX was attenuated.CONCLUSIONThis study shows that, as expected, OVX increases adiposity. However, contrary to previous effects seen in obese mice, this did not prevent fermentation of HAM-RS2 and consequently, the fat gain associated with OVX was attenuated.
Author Janes, Marlene
Robert, Julina
Raggio, Anne M.
Tulley, Richard
Senevirathne, Reshani N.
Keenan, Michael J.
Pelkman, Christine
McCutcheon, Kathleen L.
Goita, M'Famara
Martin, Roy J.
Durham, Holiday A.
Zhou, June
AuthorAffiliation 5 Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA
3 Western Human Nutrition Research Center, Davis, California, USA
4 Ingredion Incorporated, Bridgewater, New Jersey, USA
2 Department of Food Science, Louisiana State University Agricultural Center, Baton Rouge, Louisiana, USA
6 Laboratory of Geriatric Endocrinology and Metabolism, Veterans Affairs Medical Center, Washington, DC, USA
1 Department of Human Ecology, Louisiana State University Agricultural Center, Baton Rouge, Louisiana, USA
AuthorAffiliation_xml – name: 4 Ingredion Incorporated, Bridgewater, New Jersey, USA
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Notes Disclosure: Michael Keenan and Roy Martin have received funding from Ingredion Incorporated for research. Christine Pelkman is an employee of Ingredion Incorporated.
Funding agencies: This study was supported with funding from Ingredion Incorporated, the Louisiana State University Agricultural Center, and the Gordon Cain Professorship in the School of Human Ecology of the College of Agriculture of Louisiana State University
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Snippet Objective: Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the...
Obesity after menopause is a health concern for older females. Changes in the microbiota are likely to occur with this condition. Modifying the microbiota with...
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SubjectTerms Adipose Tissue - drug effects
Adipose Tissue - metabolism
Animals
Bacteria
Bacteria - drug effects
Body fat
Cellulose
Deoxyribonucleic acid
Diet
Dietary Fiber - pharmacology
Dietary Fiber - therapeutic use
DNA
E coli
Female
Fermentation
Gastrointestinal Tract - microbiology
Genetic testing
Large intestine
Menopause
Methods
Microbiota
Obesity
Obesity - etiology
Obesity - microbiology
Obesity - prevention & control
Ovariectomy
Plant Preparations - pharmacology
Plant Preparations - therapeutic use
Prebiotics
Rats, Sprague-Dawley
Rodents
Starch - analogs & derivatives
Starch - pharmacology
Starch - therapeutic use
Surgery
Weight Gain - drug effects
Zea mays - chemistry
Title Resistant starch from high amylose maize (HAM‐RS2) reduces body fat and increases gut bacteria in ovariectomized (OVX) rats
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Foby.20109
https://www.ncbi.nlm.nih.gov/pubmed/23784900
https://www.proquest.com/docview/1674729977
https://www.proquest.com/docview/1370635695
https://pubmed.ncbi.nlm.nih.gov/PMC4826615
Volume 21
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