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...

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Veröffentlicht in:BioMed research international 2018-01, Vol.2018 (2018), p.1-15
Hauptverfasser: Escoto, Jorge, Valdés-Ramos, Roxana, Ramírez Durán, Ninfa, Reséndiz-Albor, Aldo Arturo, Martínez-Carrillo, Beatríz E., Rosales-Gómez, Cristian Angel, Mondragón-Velásquez, Talia
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container_end_page 15
container_issue 2018
container_start_page 1
container_title BioMed research international
container_volume 2018
creator Escoto, Jorge
Valdés-Ramos, Roxana
Ramírez Durán, Ninfa
Reséndiz-Albor, Aldo Arturo
Martínez-Carrillo, Beatríz E.
Rosales-Gómez, Cristian Angel
Mondragón-Velásquez, Talia
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.
doi_str_mv 10.1155/2018/1345282
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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.</description><identifier>ISSN: 2314-6133</identifier><identifier>ISSN: 2314-6141</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2018/1345282</identifier><identifier>PMID: 29854725</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animals ; Antigens ; Appetite ; B cells ; B-Lymphocytes - drug effects ; B-Lymphocytes - immunology ; Beta cells ; Blood glucose ; Blood Glucose - drug effects ; Blood sugar ; Body weight ; CD19 antigen ; CD3 antigen ; Chemistry ; Consumption data ; Cytokines ; Disease Models, Animal ; Food ; Food consumption ; Food intake ; Hormones ; Humans ; Immune response ; Immunoglobulin A ; Immunology ; Insulin ; Insulin - metabolism ; Insulin Resistance ; Interleukin 4 ; Interleukin 5 ; Intestinal Mucosa - drug effects ; Intestinal Mucosa - immunology ; Intestine ; Laboratory animals ; Lamina propria ; Leptin ; Lymphocytes ; Lymphocytes - drug effects ; Lymphocytes - immunology ; Lymphocytes T ; Lymphoid Tissue - drug effects ; Lymphoid Tissue - immunology ; Medical equipment and supplies industry ; Medical test kit industry ; Metabolism ; Mice ; Morphology ; Mucosa ; Nutrition research ; Obesity ; Pathogens ; Plasma cells ; Rodents ; Small intestine ; Subgroups ; Sucralose ; Sucrose ; Sugar ; Sweeteners ; Sweetening Agents - administration &amp; dosage ; Sweetening Agents - adverse effects ; T cells ; T-Lymphocytes - drug effects ; T-Lymphocytes - immunology ; Toxicology ; Tumor necrosis factor ; Type 2 diabetes ; Weight reduction ; γ-Interferon</subject><ispartof>BioMed research international, 2018-01, Vol.2018 (2018), p.1-15</ispartof><rights>Copyright © 2018 Cristian Angel Rosales-Gómez et al.</rights><rights>COPYRIGHT 2018 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2018 Cristian Angel Rosales-Gómez et al.; 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.</rights><rights>Copyright © 2018 Cristian Angel Rosales-Gómez et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-b260144342f971bd372a11c7571814eff92551288e69a4347b224bd114372cf03</citedby><cites>FETCH-LOGICAL-c499t-b260144342f971bd372a11c7571814eff92551288e69a4347b224bd114372cf03</cites><orcidid>0000-0002-6256-3285 ; 0000-0001-6364-0775 ; 0000-0003-1415-5524 ; 0000-0002-2663-5202 ; 0000-0003-0093-886X ; 0000-0001-7009-5998</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941818/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941818/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29854725$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Li, Yin</contributor><contributor>Yin Li</contributor><creatorcontrib>Escoto, Jorge</creatorcontrib><creatorcontrib>Valdés-Ramos, Roxana</creatorcontrib><creatorcontrib>Ramírez Durán, Ninfa</creatorcontrib><creatorcontrib>Reséndiz-Albor, Aldo Arturo</creatorcontrib><creatorcontrib>Martínez-Carrillo, Beatríz E.</creatorcontrib><creatorcontrib>Rosales-Gómez, Cristian Angel</creatorcontrib><creatorcontrib>Mondragón-Velásquez, Talia</creatorcontrib><title>Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><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.</description><subject>Animals</subject><subject>Antigens</subject><subject>Appetite</subject><subject>B cells</subject><subject>B-Lymphocytes - drug effects</subject><subject>B-Lymphocytes - immunology</subject><subject>Beta cells</subject><subject>Blood glucose</subject><subject>Blood Glucose - drug effects</subject><subject>Blood sugar</subject><subject>Body weight</subject><subject>CD19 antigen</subject><subject>CD3 antigen</subject><subject>Chemistry</subject><subject>Consumption data</subject><subject>Cytokines</subject><subject>Disease Models, Animal</subject><subject>Food</subject><subject>Food consumption</subject><subject>Food intake</subject><subject>Hormones</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunoglobulin A</subject><subject>Immunology</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Insulin Resistance</subject><subject>Interleukin 4</subject><subject>Interleukin 5</subject><subject>Intestinal Mucosa - drug effects</subject><subject>Intestinal Mucosa - immunology</subject><subject>Intestine</subject><subject>Laboratory animals</subject><subject>Lamina propria</subject><subject>Leptin</subject><subject>Lymphocytes</subject><subject>Lymphocytes - drug effects</subject><subject>Lymphocytes - immunology</subject><subject>Lymphocytes T</subject><subject>Lymphoid Tissue - drug effects</subject><subject>Lymphoid Tissue - immunology</subject><subject>Medical equipment and supplies industry</subject><subject>Medical test kit industry</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Morphology</subject><subject>Mucosa</subject><subject>Nutrition research</subject><subject>Obesity</subject><subject>Pathogens</subject><subject>Plasma cells</subject><subject>Rodents</subject><subject>Small intestine</subject><subject>Subgroups</subject><subject>Sucralose</subject><subject>Sucrose</subject><subject>Sugar</subject><subject>Sweeteners</subject><subject>Sweetening Agents - administration &amp; dosage</subject><subject>Sweetening Agents - adverse effects</subject><subject>T cells</subject><subject>T-Lymphocytes - drug effects</subject><subject>T-Lymphocytes - immunology</subject><subject>Toxicology</subject><subject>Tumor necrosis factor</subject><subject>Type 2 diabetes</subject><subject>Weight reduction</subject><subject>γ-Interferon</subject><issn>2314-6133</issn><issn>2314-6141</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkcFv0zAUxiMEYlPZjTOyxAWJluU5dhJfkKqwdZOKODDOluM-rx6JXeKEKv89zlo64IQvftL7-Xvv85ckryH9AMD5JU2hvISMcVrSZ8k5zYAtcmDw_FRn2VlyEcJDGk8JeSryl8kZFSVnBeXnyb7adt5ZTSrvwtDueusd8YZ83SP26LALRLkNue0DuTIGdU9if9WMWmFr1ZxUY--_W4dhTm581_rHanqxHtvd1uuxxzDprZbrO2IdqT4B-Ww1vkpeGNUEvDjes-Tb9dVddbNYf1ndVsv1QjMh-kVN8xQYyxg1ooB6kxVUAeiCF1ACQ2ME5RxoWWIuVMSKmlJWbwBYJLVJs1ny8aC7G-oWNxpd36lG7jrbqm6UXln5d8fZrbz3PyUXLI4oo8C7o0DnfwwYetnaoLFplEM_BElTJuIKPH70LHn7D_rgh85Fe5HKOKWpoPkTda8alNYZH-fqSVQucwplGoMVkZofKN35EDo0p5UhlVP0copeHqOP-Js_bZ7g30FH4P0B2Fq3UXv7n3IYGTTqiQbKaPT6C6zcvAg</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Escoto, Jorge</creator><creator>Valdés-Ramos, Roxana</creator><creator>Ramírez Durán, Ninfa</creator><creator>Reséndiz-Albor, Aldo Arturo</creator><creator>Martínez-Carrillo, Beatríz E.</creator><creator>Rosales-Gómez, Cristian Angel</creator><creator>Mondragón-Velásquez, Talia</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley &amp; 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Valdés-Ramos, Roxana ; Ramírez Durán, Ninfa ; Reséndiz-Albor, Aldo Arturo ; Martínez-Carrillo, Beatríz E. ; Rosales-Gómez, Cristian Angel ; Mondragón-Velásquez, Talia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-b260144342f971bd372a11c7571814eff92551288e69a4347b224bd114372cf03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Antigens</topic><topic>Appetite</topic><topic>B cells</topic><topic>B-Lymphocytes - drug effects</topic><topic>B-Lymphocytes - immunology</topic><topic>Beta cells</topic><topic>Blood glucose</topic><topic>Blood Glucose - drug effects</topic><topic>Blood sugar</topic><topic>Body weight</topic><topic>CD19 antigen</topic><topic>CD3 antigen</topic><topic>Chemistry</topic><topic>Consumption data</topic><topic>Cytokines</topic><topic>Disease Models, Animal</topic><topic>Food</topic><topic>Food consumption</topic><topic>Food intake</topic><topic>Hormones</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunoglobulin A</topic><topic>Immunology</topic><topic>Insulin</topic><topic>Insulin - metabolism</topic><topic>Insulin Resistance</topic><topic>Interleukin 4</topic><topic>Interleukin 5</topic><topic>Intestinal Mucosa - drug effects</topic><topic>Intestinal Mucosa - immunology</topic><topic>Intestine</topic><topic>Laboratory animals</topic><topic>Lamina propria</topic><topic>Leptin</topic><topic>Lymphocytes</topic><topic>Lymphocytes - drug effects</topic><topic>Lymphocytes - immunology</topic><topic>Lymphocytes T</topic><topic>Lymphoid Tissue - drug effects</topic><topic>Lymphoid Tissue - immunology</topic><topic>Medical equipment and supplies industry</topic><topic>Medical test kit industry</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Morphology</topic><topic>Mucosa</topic><topic>Nutrition research</topic><topic>Obesity</topic><topic>Pathogens</topic><topic>Plasma cells</topic><topic>Rodents</topic><topic>Small intestine</topic><topic>Subgroups</topic><topic>Sucralose</topic><topic>Sucrose</topic><topic>Sugar</topic><topic>Sweeteners</topic><topic>Sweetening Agents - administration &amp; 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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.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>29854725</pmid><doi>10.1155/2018/1345282</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-6256-3285</orcidid><orcidid>https://orcid.org/0000-0001-6364-0775</orcidid><orcidid>https://orcid.org/0000-0003-1415-5524</orcidid><orcidid>https://orcid.org/0000-0002-2663-5202</orcidid><orcidid>https://orcid.org/0000-0003-0093-886X</orcidid><orcidid>https://orcid.org/0000-0001-7009-5998</orcidid><oa>free_for_read</oa></addata></record>
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2314-6141
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5941818
source Wiley-Blackwell Open Access Collection; MEDLINE; PubMed Central; Alma/SFX Local Collection; PubMed Central Open Access
subjects Animals
Antigens
Appetite
B cells
B-Lymphocytes - drug effects
B-Lymphocytes - immunology
Beta cells
Blood glucose
Blood Glucose - drug effects
Blood sugar
Body weight
CD19 antigen
CD3 antigen
Chemistry
Consumption data
Cytokines
Disease Models, Animal
Food
Food consumption
Food intake
Hormones
Humans
Immune response
Immunoglobulin A
Immunology
Insulin
Insulin - metabolism
Insulin Resistance
Interleukin 4
Interleukin 5
Intestinal Mucosa - drug effects
Intestinal Mucosa - immunology
Intestine
Laboratory animals
Lamina propria
Leptin
Lymphocytes
Lymphocytes - drug effects
Lymphocytes - immunology
Lymphocytes T
Lymphoid Tissue - drug effects
Lymphoid Tissue - immunology
Medical equipment and supplies industry
Medical test kit industry
Metabolism
Mice
Morphology
Mucosa
Nutrition research
Obesity
Pathogens
Plasma cells
Rodents
Small intestine
Subgroups
Sucralose
Sucrose
Sugar
Sweeteners
Sweetening Agents - administration & dosage
Sweetening Agents - adverse effects
T cells
T-Lymphocytes - drug effects
T-Lymphocytes - immunology
Toxicology
Tumor necrosis factor
Type 2 diabetes
Weight reduction
γ-Interferon
title Chronic Consumption of Sweeteners and Its Effect on Glycaemia, Cytokines, Hormones, and Lymphocytes of GALT in CD1 Mice
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