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Effect of functional food ingredients on gut microbiota in a rodent diabetes model

BACKGROUND: The gut microbiota has been shown to be involved in the development and severity of type 2 diabetes. The aim of the present study was to test the effect of 4-week functional food ingredient feeding, alone or in combination, on the gut microbiota composition in diabetic rats. METHODS: Str...

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Autores principales: Surono, Ingrid S., Wardana, Ata Aditya, Waspodo, Priyo, Saksono, Budi, Verhoeven, Jessica, Venema, Koen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501656/
https://www.ncbi.nlm.nih.gov/pubmed/32968426
http://dx.doi.org/10.1186/s12986-020-00496-2
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author Surono, Ingrid S.
Wardana, Ata Aditya
Waspodo, Priyo
Saksono, Budi
Verhoeven, Jessica
Venema, Koen
author_facet Surono, Ingrid S.
Wardana, Ata Aditya
Waspodo, Priyo
Saksono, Budi
Verhoeven, Jessica
Venema, Koen
author_sort Surono, Ingrid S.
collection PubMed
description BACKGROUND: The gut microbiota has been shown to be involved in the development and severity of type 2 diabetes. The aim of the present study was to test the effect of 4-week functional food ingredient feeding, alone or in combination, on the gut microbiota composition in diabetic rats. METHODS: Streptozotocin (STZ)-induced diabetic rats were treated for 4 weeks with (1) native taro starch, (2) modified taro-starch, (3) beet juice, (4) psicose, (5) the probiotic L. plantarum IS-10506, (6) native starch combined with beet juice, (7) native starch to which beet juice was adsorbed, (8) modified starch combined with beet juice or (9) modified starch to which beet juice was adsorbed, to modulate the composition of the gut microbiota. This composition was evaluated by sequencing the PCR amplified V3–V4 region of the 16S rRNA gene. RESULTS: The next-generation sequencing showed beneficial effects particularly of taro-starch feeding. Operational taxonomic units (OTUs) related to health (e.g. correlating with low BMI, OTUs producing butyrate) were increased in relative abundance, while OTUs generally correlated with disease (e.g. Proteobacteria) were decreased by feeding taro-starch. CONCLUSION: The results of study show that a 4-week intervention with functional food ingredients, particularly taro-derived starch, leads to a more healthy gut microbiota in rats that were induced to be diabetic by induction with STZ.
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spelling pubmed-75016562020-09-22 Effect of functional food ingredients on gut microbiota in a rodent diabetes model Surono, Ingrid S. Wardana, Ata Aditya Waspodo, Priyo Saksono, Budi Verhoeven, Jessica Venema, Koen Nutr Metab (Lond) Research BACKGROUND: The gut microbiota has been shown to be involved in the development and severity of type 2 diabetes. The aim of the present study was to test the effect of 4-week functional food ingredient feeding, alone or in combination, on the gut microbiota composition in diabetic rats. METHODS: Streptozotocin (STZ)-induced diabetic rats were treated for 4 weeks with (1) native taro starch, (2) modified taro-starch, (3) beet juice, (4) psicose, (5) the probiotic L. plantarum IS-10506, (6) native starch combined with beet juice, (7) native starch to which beet juice was adsorbed, (8) modified starch combined with beet juice or (9) modified starch to which beet juice was adsorbed, to modulate the composition of the gut microbiota. This composition was evaluated by sequencing the PCR amplified V3–V4 region of the 16S rRNA gene. RESULTS: The next-generation sequencing showed beneficial effects particularly of taro-starch feeding. Operational taxonomic units (OTUs) related to health (e.g. correlating with low BMI, OTUs producing butyrate) were increased in relative abundance, while OTUs generally correlated with disease (e.g. Proteobacteria) were decreased by feeding taro-starch. CONCLUSION: The results of study show that a 4-week intervention with functional food ingredients, particularly taro-derived starch, leads to a more healthy gut microbiota in rats that were induced to be diabetic by induction with STZ. BioMed Central 2020-09-18 /pmc/articles/PMC7501656/ /pubmed/32968426 http://dx.doi.org/10.1186/s12986-020-00496-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Surono, Ingrid S.
Wardana, Ata Aditya
Waspodo, Priyo
Saksono, Budi
Verhoeven, Jessica
Venema, Koen
Effect of functional food ingredients on gut microbiota in a rodent diabetes model
title Effect of functional food ingredients on gut microbiota in a rodent diabetes model
title_full Effect of functional food ingredients on gut microbiota in a rodent diabetes model
title_fullStr Effect of functional food ingredients on gut microbiota in a rodent diabetes model
title_full_unstemmed Effect of functional food ingredients on gut microbiota in a rodent diabetes model
title_short Effect of functional food ingredients on gut microbiota in a rodent diabetes model
title_sort effect of functional food ingredients on gut microbiota in a rodent diabetes model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501656/
https://www.ncbi.nlm.nih.gov/pubmed/32968426
http://dx.doi.org/10.1186/s12986-020-00496-2
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