Abstract | OBJECTIVE: The effects of type 2 resistant starch from high- amylose maize (HAM-RS2) in rodents fed with low-fat diets were demonstrated in previous studies. Fish oil is also reported to reduce body fat. In the current study, the effects of high fat and fish oil on HAM-RS2 feeding in rats were investigated. DESIGN AND METHODS: Rats were fed 0 or 27% (weight) HAM-RS2 with low (15% energy) or high fat (42% energy) diets that included 0 or 10% (energy) tuna oil to test the effect of HAM-RS2 in diet-induced obesity and effects of tuna oil. Data were analyzed as 2 × 2 × 2 factorial. RESULTS: Rats fed HAM-RS2 had decreased cecal contents pH, increased cecal and cecal contents weight, increased cecal contents acetate, propionate, and butyrate, increased GLP-1 and PYY, and decreased abdominal fat. However, high fat partially attenuated effects of HAM-RS2, but increased GLP-1 active. Dietary tuna oil had limited effects at concentration used. CONCLUSIONS: Results demonstrated that a high fat diet partially attenuates the response to HAM-RS2. The mechanism may center on reduced levels of cecal contents propionate and butyrate and reduced serum PYY. This study demonstrated that with consumption of high fat, HAM-RS2 produces fermentation but results in partial attenuation of effects.
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Authors | Jason A Charrier, Roy J Martin, Kathleen L McCutcheon, Anne M Raggio, Felicia Goldsmith, M'famara Goita, Reshani N Senevirathne, Ian L Brown, Christine Pelkman, June Zhou, John Finley, Holiday A Durham, Michael J Keenan |
Journal | Obesity (Silver Spring, Md.)
(Obesity (Silver Spring))
Vol. 21
Issue 11
Pg. 2350-5
(Nov 2013)
ISSN: 1930-739X [Electronic] United States |
PMID | 23512798
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 The Obesity Society. |
Chemical References |
- Dietary Fats
- Starch
- Amylose
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Topics |
- Abdominal Fat
(anatomy & histology)
- Amylose
(metabolism)
- Animals
- Body Weight
(drug effects)
- Diet, High-Fat
- Dietary Fats
(pharmacology)
- Eating
(physiology)
- Energy Intake
(physiology)
- Fermentation
(drug effects)
- Male
- Rats
- Rats, Sprague-Dawley
- Starch
(metabolism)
- Zea mays
(metabolism)
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