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Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice
BACKGROUND: The consumption of sweeteners has increased in recent years, being used to control body weight and blood glucose. However, they can cause increased appetite, modification of immune function, and secretion of hormones in the GALT. OBJECTIVE: To assess the effect of chronic sweetener consu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941818/ https://www.ncbi.nlm.nih.gov/pubmed/29854725 http://dx.doi.org/10.1155/2018/1345282 |
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author | Rosales-Gómez, Cristian Angel Martínez-Carrillo, Beatriz Elina Reséndiz-Albor, Aldo Arturo Ramírez-Durán, Ninfa Valdés-Ramos, Roxana Mondragón-Velásquez, Talia Escoto-Herrera, Jorge Alberto |
author_facet | Rosales-Gómez, Cristian Angel Martínez-Carrillo, Beatriz Elina Reséndiz-Albor, Aldo Arturo Ramírez-Durán, Ninfa Valdés-Ramos, Roxana Mondragón-Velásquez, Talia Escoto-Herrera, Jorge Alberto |
author_sort | Rosales-Gómez, Cristian Angel |
collection | PubMed |
description | BACKGROUND: The consumption of sweeteners has increased in recent years, being used to control body weight and blood glucose. However, they can cause increased appetite, modification of immune function, and secretion of hormones in the GALT. OBJECTIVE: To assess the effect of chronic sweetener consumption on glycaemia, cytokines, hormones, and GALT lymphocytes in CD1 mice. MATERIAL AND METHODS: 72 CD1 mice divided into 3 groups were used: (a) baseline, (b) middle, and (c) final. Groups (b) and (c) were divided into 4 subgroups: (i) Control, (ii) Sucrose, (iii) Sucralose, and (iv) Stevia. The following were determined: body weight, hormones (GIP, insulin, and leptin), lymphocytes CD3(+)T cells and CD19(+)B cells, IgA(+) plasma cells, and cytokines (IL-4, IL-5, IFN-γ, and TNF-α). RESULTS: Sucralose reduces secretion of GIP and glycaemia but does not modify insulin concentration, increases body weight, and reduces food intake. Stevia increases the secretion of GIP, insulin, leptin, body weight, and glycaemia but keeps food consumption normal. Sucralose and Stevia showed a higher percentage of CD3(+)T cells, CD19(+)B cells, and IgA(+) plasma cells in Peyer's patches, but only Stevia in lamina propria. CONCLUSION: Sweeteners modulate the hormonal response of cytokines and the proliferation of lymphocytes in the intestinal mucosa. |
format | Online Article Text |
id | pubmed-5941818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-59418182018-05-31 Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice Rosales-Gómez, Cristian Angel Martínez-Carrillo, Beatriz Elina Reséndiz-Albor, Aldo Arturo Ramírez-Durán, Ninfa Valdés-Ramos, Roxana Mondragón-Velásquez, Talia Escoto-Herrera, Jorge Alberto Biomed Res Int Research Article BACKGROUND: The consumption of sweeteners has increased in recent years, being used to control body weight and blood glucose. However, they can cause increased appetite, modification of immune function, and secretion of hormones in the GALT. OBJECTIVE: To assess the effect of chronic sweetener consumption on glycaemia, cytokines, hormones, and GALT lymphocytes in CD1 mice. MATERIAL AND METHODS: 72 CD1 mice divided into 3 groups were used: (a) baseline, (b) middle, and (c) final. Groups (b) and (c) were divided into 4 subgroups: (i) Control, (ii) Sucrose, (iii) Sucralose, and (iv) Stevia. The following were determined: body weight, hormones (GIP, insulin, and leptin), lymphocytes CD3(+)T cells and CD19(+)B cells, IgA(+) plasma cells, and cytokines (IL-4, IL-5, IFN-γ, and TNF-α). RESULTS: Sucralose reduces secretion of GIP and glycaemia but does not modify insulin concentration, increases body weight, and reduces food intake. Stevia increases the secretion of GIP, insulin, leptin, body weight, and glycaemia but keeps food consumption normal. Sucralose and Stevia showed a higher percentage of CD3(+)T cells, CD19(+)B cells, and IgA(+) plasma cells in Peyer's patches, but only Stevia in lamina propria. CONCLUSION: Sweeteners modulate the hormonal response of cytokines and the proliferation of lymphocytes in the intestinal mucosa. Hindawi 2018-04-24 /pmc/articles/PMC5941818/ /pubmed/29854725 http://dx.doi.org/10.1155/2018/1345282 Text en Copyright © 2018 Cristian Angel Rosales-Gómez et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rosales-Gómez, Cristian Angel Martínez-Carrillo, Beatriz Elina Reséndiz-Albor, Aldo Arturo Ramírez-Durán, Ninfa Valdés-Ramos, Roxana Mondragón-Velásquez, Talia Escoto-Herrera, Jorge Alberto Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice |
title | Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice |
title_full | Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice |
title_fullStr | Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice |
title_full_unstemmed | Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice |
title_short | Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice |
title_sort | chronic consumption of sweeteners and its effect on glycaemia, cytokines, hormones, and lymphocytes of galt in cd1 mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941818/ https://www.ncbi.nlm.nih.gov/pubmed/29854725 http://dx.doi.org/10.1155/2018/1345282 |
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