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- Title
Rice bran triterpenoids improve postprandial hyperglycemia in healthy male adults: a randomized, double-blind, placebo-controlled study.
- Authors
Koichi Misawa; Hiroko Jokura; Akira Shimotoyodome
- Abstract
Background: Compared to white rice, brown rice induces a lower glycemic response in healthy and diabetic humans. This effect is partly attributed to the higher amounts of water- or oil-soluble bran components and dietary fiber in brown rice. We hypothesized that dietary supplementation with oil-soluble rice bran triterpenoids (RBTs; triterpene alcohol and sterol prepared from rice bran) might reduce the incidence of postprandial hyperglycemia in healthy humans. Objective: We examined the acute effects of a single RBT-supplemented meal on the postprandial blood glucose responses of healthy male adults in a double-blind, randomized, placebo-controlled, crossover trial. Design: Nineteen subjects consumed a test meal containing either placebo- or RBT-supplemented olive oil. Blood biomarkers were evaluated in a fasting state and up to 240 min postprandially. Results: Compared to the placebo-supplemented meal, the RBT-supplemented meal significantly suppressed the increase in postprandial blood glucose level. A subclass analysis revealed that RBT-supplemented oil significantly reduced blood glucose increases in subjects with higher postprandial blood glucose elevations. Postprandial increases in blood insulin, glucose-dependent insulinotropic peptide (GIP), and glucagon-like peptide-1 (GLP-1) levels did not differ between the groups. Conclusion: These results suggest that RBT consumption improves postprandial hyperglycemia in healthy humans, especially those with higher postprandial glucose increases.
- Subjects
HYPERGLYCEMIA prevention; BLOOD sugar; CROSSOVER trials; DIETARY supplements; GASTROINTESTINAL hormones; INGESTION; INSULIN; MEN'S health; OLIVE oil; RICE oil; TERPENES; RANDOMIZED controlled trials; DISEASE incidence; BLIND experiment
- Publication
Food & Nutrition Research, 2018, Vol 62, p1
- ISSN
1654-6628
- Publication type
Article
- DOI
10.29219/fnr.v62.1412