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L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses
BACKGROUND: Diets inducing high fluctuations in plasma glucose levels are linked to type 2 diabetes. L-arabinose and D-xylose have been hypothesized to inhibit intestinal sucrase activity, delay sucrose digestion, and reduce glycaemic and insulinaemic responses. However, few human studies have asses...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Open Academia
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344406/ https://www.ncbi.nlm.nih.gov/pubmed/34393698 http://dx.doi.org/10.29219/fnr.v65.6254 |
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author | Pol, Korrie Mars, Monica |
author_facet | Pol, Korrie Mars, Monica |
author_sort | Pol, Korrie |
collection | PubMed |
description | BACKGROUND: Diets inducing high fluctuations in plasma glucose levels are linked to type 2 diabetes. L-arabinose and D-xylose have been hypothesized to inhibit intestinal sucrase activity, delay sucrose digestion, and reduce glycaemic and insulinaemic responses. However, few human studies have assessed this using realistic foods. OBJECTIVE: We investigated the effects of the addition of L-arabinose and D-xylose on glucose homeostasis using a fruit-based drink and the effect of L-arabinose using a muffin. DESIGN: Fifteen males participated in two double-blind, randomized cross-over experiments. In experiment A, three drinks were tested: (1) L-arabinose, (2) D-xylose and (3) control drink. In experiment B, two muffins were tested: (1) L-arabinose and (2) control muffin. All products consisted of ~50 g available carbohydrates, and L-arabinose or D-xylose was added as 10% of sucrose. Pre- and post-ingestive plasma glucose and insulin levels were measured at fixed time points up to 180 min after consumption. RESULTS: Glucose and insulin peaks were lower after the L-arabinose and D-xylose drink than the control drink (P < 0.01). After consumption of the muffin, glucose responses were not significantly different; however, the insulin peak and incremental area under the curve (iAUC) tended to be lower for the L-arabinose muffin. CONCLUSION: L-arabinose and D-xylose are functional ingredients that can potentially lower the post-ingestive glycaemic and insulinaemic responses when added to realistic foods. However, the efficacy of applying L-arabinose appears to depend on the food matrix. Addition of these compounds needs further testing in other foods and in other populations, such as pre-diabetics. |
format | Online Article Text |
id | pubmed-8344406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Open Academia |
record_format | MEDLINE/PubMed |
spelling | pubmed-83444062021-08-13 L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses Pol, Korrie Mars, Monica Food Nutr Res Original Article BACKGROUND: Diets inducing high fluctuations in plasma glucose levels are linked to type 2 diabetes. L-arabinose and D-xylose have been hypothesized to inhibit intestinal sucrase activity, delay sucrose digestion, and reduce glycaemic and insulinaemic responses. However, few human studies have assessed this using realistic foods. OBJECTIVE: We investigated the effects of the addition of L-arabinose and D-xylose on glucose homeostasis using a fruit-based drink and the effect of L-arabinose using a muffin. DESIGN: Fifteen males participated in two double-blind, randomized cross-over experiments. In experiment A, three drinks were tested: (1) L-arabinose, (2) D-xylose and (3) control drink. In experiment B, two muffins were tested: (1) L-arabinose and (2) control muffin. All products consisted of ~50 g available carbohydrates, and L-arabinose or D-xylose was added as 10% of sucrose. Pre- and post-ingestive plasma glucose and insulin levels were measured at fixed time points up to 180 min after consumption. RESULTS: Glucose and insulin peaks were lower after the L-arabinose and D-xylose drink than the control drink (P < 0.01). After consumption of the muffin, glucose responses were not significantly different; however, the insulin peak and incremental area under the curve (iAUC) tended to be lower for the L-arabinose muffin. CONCLUSION: L-arabinose and D-xylose are functional ingredients that can potentially lower the post-ingestive glycaemic and insulinaemic responses when added to realistic foods. However, the efficacy of applying L-arabinose appears to depend on the food matrix. Addition of these compounds needs further testing in other foods and in other populations, such as pre-diabetics. Open Academia 2021-07-23 /pmc/articles/PMC8344406/ /pubmed/34393698 http://dx.doi.org/10.29219/fnr.v65.6254 Text en © 2021 Korrie Pol and Monica Mars https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license. |
spellingShingle | Original Article Pol, Korrie Mars, Monica L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses |
title | L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses |
title_full | L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses |
title_fullStr | L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses |
title_full_unstemmed | L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses |
title_short | L-arabinose and D-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses |
title_sort | l-arabinose and d-xylose: sweet pentoses that may reduce postprandial glucose and insulin responses |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344406/ https://www.ncbi.nlm.nih.gov/pubmed/34393698 http://dx.doi.org/10.29219/fnr.v65.6254 |
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