High-amylose resistant starch increases hormones and improves structure and function of the gastrointestinal tract: a
Michael J Keenan1, Roy J Martin, Anne M Raggio
1Louisiana State University Agricultural Center, Baton Rouge, LA, USA. mkeenan@agctr.lsu.edu
Journal of Nutrigenetics and Nutrigenomics
|April 21, 2012
Summary
High-amylose maize resistant starch (HAM-RS2) promotes gut health by altering gene expression in rats. Feeding HAM-RS2 supports cell growth and increases gut hormones like GLP-1 and PYY.
Area of Science:
- Nutritional Science
- Molecular Biology
- Gastroenterology
Background:
- Type 2 resistant starch from high-amylose maize (HAM-RS2) enhances gut fermentation and increases expression of proglucagon (GLP-1) and peptide YY (PYY) genes.
- Previous research indicates HAM-RS2 consumption is linked to improved health outcomes.
Purpose of the Study:
- To investigate the comprehensive gene expression changes (upregulation and downregulation) induced by feeding HAM-RS2.
- To identify additional genes affected by HAM-RS2 beyond those related to GLP-1 and PYY.
Main Methods:
- Adult male Sprague Dawley rats were assigned to three dietary groups for 4 weeks: cornstarch control (CC), energy density control (EC), and 30% HAM-RS2 (RS).
- Gene expression profiling was conducted using rat microarrays (approximately 27,000 genes) and validated with quantitative PCR (qPCR) on cecal cell RNA.
- The comparison between RS and EC diets controlled for energy density to isolate the effects of fermentation.
Main Results:
- Microarray analysis revealed that 86% of genes were validated in the RS versus EC comparison.
- Gene expression changes indicated promotion of cell growth, proliferation, differentiation, and apoptosis in the cecum.
- Significant increases in gut hormones GLP-1 and PYY were observed.
Conclusions:
- The observed gene expression patterns suggest that HAM-RS2 consumption leads to improvements in the structure and function of the gastrointestinal tract.
- The production of gut hormones like GLP-1 and PYY may contribute to beneficial health effects extending beyond the GI tract.
Related Concept Videos
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are typically...
Acarbose and miglitol are typically...
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention
Improving a drug's stability in the gastrointestinal (GI) tract is paramount for enhancing its bioavailability and therapeutic effectiveness. Various strategies are employed to protect the drug from the harsh gastric milieu and to ensure its release and absorption at the desired site within the GI tract.Polymer coatings are one such method used to shield drugs from the stomach's acidic environment. By preventing premature drug release, these coatings improve the bioavailability of unstable...
Glucagon-like Receptor Agonists
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
Hormonal Regulation
Hormones regulate a significant portion of digestion through activation of the neuroendocrine system. The neuroendocrine system of digestion contains many different hormones all with multiple functions that are both, directly and indirectly, involved in digestion.
Carbohydrate Digestion
Carbohydrate digestion and metabolism break down simple and complex carbohydrates from food into saccharides (i.e., sugars) for the body to use as energy. Carbohydrate digestion starts in the mouth during mastication, or chewing. The masticated carbohydrates remain intact in the stomach. Digestion resumes in the duodenum of the small intestine, where pancreatic alpha-amylase and brush border enzymes of the microvilli convert complex carbohydrates to monosaccharides. Finally, the monosaccharides...
Hormones Secreted by the Stomach
Enteroendocrine cells, accounting for only 1% of stomach epithelial cells, play a significant role in digestion and are classified by their digestive hormone secretions.
Each of these hormones secreted by different enteroendocrine cells plays a unique role in digestion. Here are a few examples:
Each of these hormones secreted by different enteroendocrine cells plays a unique role in digestion. Here are a few examples:


