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In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts

SCOPE: Known pharmacological activities of guava (Psidium guajava) include modulation of blood glucose levels. However, mechanistic details remain unclear in many cases. METHODS AND RESULTS: This study investigated the effects of different guava leaf and fruit extracts on intestinal glucose transpor...

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Autores principales: Müller, Ulrike, Stübl, Flora, Schwarzinger, Bettina, Sandner, Georg, Iken, Marcus, Himmelsbach, Markus, Schwarzinger, Clemens, Ollinger, Nicole, Stadlbauer, Verena, Höglinger, Otmar, Kühne, Tobias, Lanzerstorfer, Peter, Weghuber, Julian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001447/
https://www.ncbi.nlm.nih.gov/pubmed/29688623
http://dx.doi.org/10.1002/mnfr.201701012
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author Müller, Ulrike
Stübl, Flora
Schwarzinger, Bettina
Sandner, Georg
Iken, Marcus
Himmelsbach, Markus
Schwarzinger, Clemens
Ollinger, Nicole
Stadlbauer, Verena
Höglinger, Otmar
Kühne, Tobias
Lanzerstorfer, Peter
Weghuber, Julian
author_facet Müller, Ulrike
Stübl, Flora
Schwarzinger, Bettina
Sandner, Georg
Iken, Marcus
Himmelsbach, Markus
Schwarzinger, Clemens
Ollinger, Nicole
Stadlbauer, Verena
Höglinger, Otmar
Kühne, Tobias
Lanzerstorfer, Peter
Weghuber, Julian
author_sort Müller, Ulrike
collection PubMed
description SCOPE: Known pharmacological activities of guava (Psidium guajava) include modulation of blood glucose levels. However, mechanistic details remain unclear in many cases. METHODS AND RESULTS: This study investigated the effects of different guava leaf and fruit extracts on intestinal glucose transport in vitro and on postprandial glucose levels in vivo. Substantial dose‐ and time‐dependent glucose transport inhibition (up to 80%) was observed for both guava fruit and leaf extracts, at conceivable physiological concentrations in Caco‐2 cells. Using sodium‐containing (both glucose transporters, sodium‐dependent glucose transporter 1 [SGLT1] and glucose transporter 2 [GLUT2], are active) and sodium‐free (only GLUT2 is active) conditions, we show that inhibition of GLUT2 was greater than that of SGLT1. Inhibitory properties of guava extracts also remained stable after digestive juice treatment, indicating a good chemical stability of the active substances. Furthermore, we could unequivocally show that guava extracts significantly reduced blood glucose levels (≈fourfold reduction) in a time‐dependent manner in vivo (C57BL/6N mice). Extracts were characterized with respect to their main putative bioactive compounds (polyphenols) using HPLC and LC‐MS. CONCLUSION: The data demonstrated that guava leaf and fruit extracts can potentially contribute to the regulation of blood glucose levels.
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spelling pubmed-60014472018-06-21 In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts Müller, Ulrike Stübl, Flora Schwarzinger, Bettina Sandner, Georg Iken, Marcus Himmelsbach, Markus Schwarzinger, Clemens Ollinger, Nicole Stadlbauer, Verena Höglinger, Otmar Kühne, Tobias Lanzerstorfer, Peter Weghuber, Julian Mol Nutr Food Res Research Articles SCOPE: Known pharmacological activities of guava (Psidium guajava) include modulation of blood glucose levels. However, mechanistic details remain unclear in many cases. METHODS AND RESULTS: This study investigated the effects of different guava leaf and fruit extracts on intestinal glucose transport in vitro and on postprandial glucose levels in vivo. Substantial dose‐ and time‐dependent glucose transport inhibition (up to 80%) was observed for both guava fruit and leaf extracts, at conceivable physiological concentrations in Caco‐2 cells. Using sodium‐containing (both glucose transporters, sodium‐dependent glucose transporter 1 [SGLT1] and glucose transporter 2 [GLUT2], are active) and sodium‐free (only GLUT2 is active) conditions, we show that inhibition of GLUT2 was greater than that of SGLT1. Inhibitory properties of guava extracts also remained stable after digestive juice treatment, indicating a good chemical stability of the active substances. Furthermore, we could unequivocally show that guava extracts significantly reduced blood glucose levels (≈fourfold reduction) in a time‐dependent manner in vivo (C57BL/6N mice). Extracts were characterized with respect to their main putative bioactive compounds (polyphenols) using HPLC and LC‐MS. CONCLUSION: The data demonstrated that guava leaf and fruit extracts can potentially contribute to the regulation of blood glucose levels. John Wiley and Sons Inc. 2018-05-17 2018-06 /pmc/articles/PMC6001447/ /pubmed/29688623 http://dx.doi.org/10.1002/mnfr.201701012 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Müller, Ulrike
Stübl, Flora
Schwarzinger, Bettina
Sandner, Georg
Iken, Marcus
Himmelsbach, Markus
Schwarzinger, Clemens
Ollinger, Nicole
Stadlbauer, Verena
Höglinger, Otmar
Kühne, Tobias
Lanzerstorfer, Peter
Weghuber, Julian
In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts
title In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts
title_full In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts
title_fullStr In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts
title_full_unstemmed In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts
title_short In Vitro and In Vivo Inhibition of Intestinal Glucose Transport by Guava (Psidium Guajava) Extracts
title_sort in vitro and in vivo inhibition of intestinal glucose transport by guava (psidium guajava) extracts
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001447/
https://www.ncbi.nlm.nih.gov/pubmed/29688623
http://dx.doi.org/10.1002/mnfr.201701012
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