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Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado

INTRODUCTION: Sweeteners are additives used in different foods. They can be natural (sucrose and stevia) or artificial (sucralose). Currently, they are routinely consumed in multiple products and their effects on the mucosa of the small intestine and its microbiota are still controversial. OBJECTIVE...

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Autores principales: Escoto, Jorge Alberto, Martínez-Carrillo, Beatriz Elina, Ramírez-Durán, Ninfa, Ramírez-Saad, Hugo, Aguirre-Garrido, José Félix, Valdés-Ramos, Roxana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Nacional de Salud 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519602/
https://www.ncbi.nlm.nih.gov/pubmed/34559497
http://dx.doi.org/10.7705/biomedica.5806
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author Escoto, Jorge Alberto
Martínez-Carrillo, Beatriz Elina
Ramírez-Durán, Ninfa
Ramírez-Saad, Hugo
Aguirre-Garrido, José Félix
Valdés-Ramos, Roxana
author_facet Escoto, Jorge Alberto
Martínez-Carrillo, Beatriz Elina
Ramírez-Durán, Ninfa
Ramírez-Saad, Hugo
Aguirre-Garrido, José Félix
Valdés-Ramos, Roxana
author_sort Escoto, Jorge Alberto
collection PubMed
description INTRODUCTION: Sweeteners are additives used in different foods. They can be natural (sucrose and stevia) or artificial (sucralose). Currently, they are routinely consumed in multiple products and their effects on the mucosa of the small intestine and its microbiota are still controversial. OBJECTIVE: To relate the consumption of sweeteners and their effect on the immune system and the microbiota of the small intestine in CD1 mice. MATERIALS AND METHODS: We used 54 three-week-old CD1 mice divided into three groups in the experiments: 1) A group of three weeks without treatment, 2) a group treated for six weeks, and 3) a group treated for 12 weeks using sucrose, sucralose, and stevia. We obtained CD19+ B lymphocytes, IgA+ antibodies, transforming growth factor-beta (TGF-b), and interleukins 12 and 17 (IL-12 and -17) from Peyer's patches and lamina propria cells while DNA was obtained from intestinal solids to identify bacterial species. RESULTS: After 12 weeks, sucrose and sucralose consumption caused a reduction in bacterial communities with an increase in CD19+, a decrease in IgA+ and TGF-b, and an increase in IL-12 and -17 in the Peyer's patches while in the lamina propria there was an increase in all parameters. In contrast, stevia led to an improvement in bacterial diversity and percentage of CD19+ lymphocytes with minimal increase in IgA+, TGF-b, and IL-12, and a decrease in IL-17. CONCLUSION: Sucrose and sucralose caused negative alterations in bacterial diversity and immune parameters after 12 weeks; in contrast, stevia was beneficial for the intestinal mucosa.
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spelling pubmed-85196022021-10-18 Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado Escoto, Jorge Alberto Martínez-Carrillo, Beatriz Elina Ramírez-Durán, Ninfa Ramírez-Saad, Hugo Aguirre-Garrido, José Félix Valdés-Ramos, Roxana Biomedica Artículo Original INTRODUCTION: Sweeteners are additives used in different foods. They can be natural (sucrose and stevia) or artificial (sucralose). Currently, they are routinely consumed in multiple products and their effects on the mucosa of the small intestine and its microbiota are still controversial. OBJECTIVE: To relate the consumption of sweeteners and their effect on the immune system and the microbiota of the small intestine in CD1 mice. MATERIALS AND METHODS: We used 54 three-week-old CD1 mice divided into three groups in the experiments: 1) A group of three weeks without treatment, 2) a group treated for six weeks, and 3) a group treated for 12 weeks using sucrose, sucralose, and stevia. We obtained CD19+ B lymphocytes, IgA+ antibodies, transforming growth factor-beta (TGF-b), and interleukins 12 and 17 (IL-12 and -17) from Peyer's patches and lamina propria cells while DNA was obtained from intestinal solids to identify bacterial species. RESULTS: After 12 weeks, sucrose and sucralose consumption caused a reduction in bacterial communities with an increase in CD19+, a decrease in IgA+ and TGF-b, and an increase in IL-12 and -17 in the Peyer's patches while in the lamina propria there was an increase in all parameters. In contrast, stevia led to an improvement in bacterial diversity and percentage of CD19+ lymphocytes with minimal increase in IgA+, TGF-b, and IL-12, and a decrease in IL-17. CONCLUSION: Sucrose and sucralose caused negative alterations in bacterial diversity and immune parameters after 12 weeks; in contrast, stevia was beneficial for the intestinal mucosa. Instituto Nacional de Salud 2021-09-22 /pmc/articles/PMC8519602/ /pubmed/34559497 http://dx.doi.org/10.7705/biomedica.5806 Text en https://creativecommons.org/licenses/by/4.0/Este es un artículo publicado en acceso abierto bajo una licencia Creative Commons
spellingShingle Artículo Original
Escoto, Jorge Alberto
Martínez-Carrillo, Beatriz Elina
Ramírez-Durán, Ninfa
Ramírez-Saad, Hugo
Aguirre-Garrido, José Félix
Valdés-Ramos, Roxana
Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado
title Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado
title_full Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado
title_fullStr Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado
title_full_unstemmed Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado
title_short Consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado
title_sort consumo crónico de edulcorantes en ratones y su efecto sobre el sistema inmunitario y la microbiota del intestino delgado
topic Artículo Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519602/
https://www.ncbi.nlm.nih.gov/pubmed/34559497
http://dx.doi.org/10.7705/biomedica.5806
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