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Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile
BACKGROUND: Rye products have previously been shown to induce comparatively low post-prandial insulin responses; irrespectively of their glycaemic indices (GI). However, the mechanism behind this lowered insulin demand remains unknown. An improved insulin economy might contribute to the benefits see...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761418/ https://www.ncbi.nlm.nih.gov/pubmed/19781071 http://dx.doi.org/10.1186/1475-2891-8-42 |
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author | Rosén, Liza AH Silva, Lorena O Blanco Andersson, Ulrika K Holm, Cecilia Östman, Elin M Björck, Inger ME |
author_facet | Rosén, Liza AH Silva, Lorena O Blanco Andersson, Ulrika K Holm, Cecilia Östman, Elin M Björck, Inger ME |
author_sort | Rosén, Liza AH |
collection | PubMed |
description | BACKGROUND: Rye products have previously been shown to induce comparatively low post-prandial insulin responses; irrespectively of their glycaemic indices (GI). However, the mechanism behind this lowered insulin demand remains unknown. An improved insulin economy might contribute to the benefits seen in epidemiological studies with whole grain diets on metabolic risk factors and weight regulation. The objective of this study was to explore the mechanism for a reduced post-prandial insulin demand with rye products. METHODS: 12 healthy subjects were given flour based rye products made from endosperm, whole grain or bran, produced with different methods (baking, simulated sour-dough baking and boiling) as breakfasts in random order in a cross-over design. White wheat bread (WWB) was used as a reference. Blood glucose, serum insulin, plasma ghrelin and subjective satiety were measured during 180 minutes. To evaluate the course of post-meal glycaemia, a measure of the glycaemic profile (GP) was introduced defined as the duration for the incremental post-prandial blood glucose response divided with the blood glucose incremental peak (min/mM). RESULTS: The study shows that whole grain rye breads and endosperm rye products induced significantly (p < 0.05) lower insulinaemic indices (II's) than WWB. Rye bran bread (RBB) produced significantly higher II compared with all the other rye products. Furthermore, the acute insulin response showed better correlations with the GP than with the GI of the products. The endosperm rye bread and the whole grain rye bread with lactic acid induced a significantly higher GP than RBB, WWB, white wheat- and whole grain rye porridge, respectively. A low insulin incremental peak was associated with less severe late post-prandial hypoglycaemia (r = 0.38, p < 0.001), and hypoglycaemia was negatively correlated to subjective satiety at 180 min (r = -0.28, p < 0.05). A low insulin incremental peak was also associated with a milder recovery of plasma ghrelin in the late post-prandial phase (180 min, r = 0.34, p < 0.01). CONCLUSION: Our study shows that endosperm and wholegrain rye products induce low acute insulinaemic responses and improved glycaemic profiles. The results also suggest that the rye products possess beneficial appetite regulating properties. Further studies are needed to identify the unknown property or bioactive component(s) responsible for these beneficial metabolic features of rye. |
format | Text |
id | pubmed-2761418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27614182009-10-14 Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile Rosén, Liza AH Silva, Lorena O Blanco Andersson, Ulrika K Holm, Cecilia Östman, Elin M Björck, Inger ME Nutr J Research BACKGROUND: Rye products have previously been shown to induce comparatively low post-prandial insulin responses; irrespectively of their glycaemic indices (GI). However, the mechanism behind this lowered insulin demand remains unknown. An improved insulin economy might contribute to the benefits seen in epidemiological studies with whole grain diets on metabolic risk factors and weight regulation. The objective of this study was to explore the mechanism for a reduced post-prandial insulin demand with rye products. METHODS: 12 healthy subjects were given flour based rye products made from endosperm, whole grain or bran, produced with different methods (baking, simulated sour-dough baking and boiling) as breakfasts in random order in a cross-over design. White wheat bread (WWB) was used as a reference. Blood glucose, serum insulin, plasma ghrelin and subjective satiety were measured during 180 minutes. To evaluate the course of post-meal glycaemia, a measure of the glycaemic profile (GP) was introduced defined as the duration for the incremental post-prandial blood glucose response divided with the blood glucose incremental peak (min/mM). RESULTS: The study shows that whole grain rye breads and endosperm rye products induced significantly (p < 0.05) lower insulinaemic indices (II's) than WWB. Rye bran bread (RBB) produced significantly higher II compared with all the other rye products. Furthermore, the acute insulin response showed better correlations with the GP than with the GI of the products. The endosperm rye bread and the whole grain rye bread with lactic acid induced a significantly higher GP than RBB, WWB, white wheat- and whole grain rye porridge, respectively. A low insulin incremental peak was associated with less severe late post-prandial hypoglycaemia (r = 0.38, p < 0.001), and hypoglycaemia was negatively correlated to subjective satiety at 180 min (r = -0.28, p < 0.05). A low insulin incremental peak was also associated with a milder recovery of plasma ghrelin in the late post-prandial phase (180 min, r = 0.34, p < 0.01). CONCLUSION: Our study shows that endosperm and wholegrain rye products induce low acute insulinaemic responses and improved glycaemic profiles. The results also suggest that the rye products possess beneficial appetite regulating properties. Further studies are needed to identify the unknown property or bioactive component(s) responsible for these beneficial metabolic features of rye. BioMed Central 2009-09-25 /pmc/articles/PMC2761418/ /pubmed/19781071 http://dx.doi.org/10.1186/1475-2891-8-42 Text en Copyright © 2009 Rosén et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Rosén, Liza AH Silva, Lorena O Blanco Andersson, Ulrika K Holm, Cecilia Östman, Elin M Björck, Inger ME Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile |
title | Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile |
title_full | Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile |
title_fullStr | Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile |
title_full_unstemmed | Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile |
title_short | Endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile |
title_sort | endosperm and whole grain rye breads are characterized by low post-prandial insulin response and a beneficial blood glucose profile |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761418/ https://www.ncbi.nlm.nih.gov/pubmed/19781071 http://dx.doi.org/10.1186/1475-2891-8-42 |
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