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Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study
BACKGROUND: The consumption of a high carbohydrate diet may be associated with an increased risk of type 2 diabetes and obesity. Previous studies in vitro have revealed that grape seed extract (GSE) inhibited the intestinal α-glucosidases and α-pancreatic amylase that may delay carbohydrate digestio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466453/ https://www.ncbi.nlm.nih.gov/pubmed/23060692 http://dx.doi.org/10.4103/0973-1296.99283 |
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author | Sapwarobol, Suwimol Adisakwattana, Sirichai Changpeng, Sawitree Ratanawachirin, Wilwan Tanruttanawong, Kanokporn Boonyarit, Waridtha |
author_facet | Sapwarobol, Suwimol Adisakwattana, Sirichai Changpeng, Sawitree Ratanawachirin, Wilwan Tanruttanawong, Kanokporn Boonyarit, Waridtha |
author_sort | Sapwarobol, Suwimol |
collection | PubMed |
description | BACKGROUND: The consumption of a high carbohydrate diet may be associated with an increased risk of type 2 diabetes and obesity. Previous studies in vitro have revealed that grape seed extract (GSE) inhibited the intestinal α-glucosidases and α-pancreatic amylase that may delay carbohydrate digestion and absorption, resulting in the suppression of postprandial glycemia. The objective of the study was to assess whether consumption of GSE together with high carbohydrate meal affects postprandial glycemia in healthy participants. MATERIALS AND METHODS: The study used acute, randomized, controlled crossover design in which eight healthy subjects (four female and four male, mean aged 21.25 ± 3.69 years; body mass index =20.28 ± 1.40 kg/m(2)) received high carbohydrate (HC) meal (73.6 %) together with or without 100 and 300 mg GSE. RESULTS: Results showed that postprandial plasma glucose concentrations at 15 min and 30 min after ingestion HC meal together with 100 mg GSE (5.33 ± 0.41 mmol/L and 5.62 ± 0.47 mmol/L, respectively) and 300 mg GSE (5.27 ± 0.29 mmol/L; 5.75 ± 0.44 mmol/L, respectively) were significantly lower than that of HC meal (P<0.05). There was statistically significant difference in the 2 h area under the glucose response curve between HC meal and HC meal plus GSE. CONCLUSIONS: GSE reduces postprandial plasma glucose in healthy participants. The delayed and attenuated hyperglycemia may have a useful strategy to prevent development of diabetes in the healthy population. |
format | Online Article Text |
id | pubmed-3466453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34664532012-10-11 Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study Sapwarobol, Suwimol Adisakwattana, Sirichai Changpeng, Sawitree Ratanawachirin, Wilwan Tanruttanawong, Kanokporn Boonyarit, Waridtha Pharmacogn Mag Original Article BACKGROUND: The consumption of a high carbohydrate diet may be associated with an increased risk of type 2 diabetes and obesity. Previous studies in vitro have revealed that grape seed extract (GSE) inhibited the intestinal α-glucosidases and α-pancreatic amylase that may delay carbohydrate digestion and absorption, resulting in the suppression of postprandial glycemia. The objective of the study was to assess whether consumption of GSE together with high carbohydrate meal affects postprandial glycemia in healthy participants. MATERIALS AND METHODS: The study used acute, randomized, controlled crossover design in which eight healthy subjects (four female and four male, mean aged 21.25 ± 3.69 years; body mass index =20.28 ± 1.40 kg/m(2)) received high carbohydrate (HC) meal (73.6 %) together with or without 100 and 300 mg GSE. RESULTS: Results showed that postprandial plasma glucose concentrations at 15 min and 30 min after ingestion HC meal together with 100 mg GSE (5.33 ± 0.41 mmol/L and 5.62 ± 0.47 mmol/L, respectively) and 300 mg GSE (5.27 ± 0.29 mmol/L; 5.75 ± 0.44 mmol/L, respectively) were significantly lower than that of HC meal (P<0.05). There was statistically significant difference in the 2 h area under the glucose response curve between HC meal and HC meal plus GSE. CONCLUSIONS: GSE reduces postprandial plasma glucose in healthy participants. The delayed and attenuated hyperglycemia may have a useful strategy to prevent development of diabetes in the healthy population. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3466453/ /pubmed/23060692 http://dx.doi.org/10.4103/0973-1296.99283 Text en Copyright: © Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sapwarobol, Suwimol Adisakwattana, Sirichai Changpeng, Sawitree Ratanawachirin, Wilwan Tanruttanawong, Kanokporn Boonyarit, Waridtha Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study |
title | Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study |
title_full | Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study |
title_fullStr | Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study |
title_full_unstemmed | Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study |
title_short | Postprandial blood glucose response to grape seed extract in healthy participants: A pilot study |
title_sort | postprandial blood glucose response to grape seed extract in healthy participants: a pilot study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466453/ https://www.ncbi.nlm.nih.gov/pubmed/23060692 http://dx.doi.org/10.4103/0973-1296.99283 |
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