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The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose

Replacing sucrose with non-caloric sweeteners is an approach to avoid overweight and diabetes development. Non-caloric sweeteners are classified into either artificial as sucralose or natural as stevia. Both of them have been approved by FDA, but the effects of their chronic consumption are controve...

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Autores principales: Farid, Alyaa, Hesham, Marim, El-Dewak, Mohamed, Amin, Ayman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584803/
https://www.ncbi.nlm.nih.gov/pubmed/33132722
http://dx.doi.org/10.1016/j.jsps.2020.08.019
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author Farid, Alyaa
Hesham, Marim
El-Dewak, Mohamed
Amin, Ayman
author_facet Farid, Alyaa
Hesham, Marim
El-Dewak, Mohamed
Amin, Ayman
author_sort Farid, Alyaa
collection PubMed
description Replacing sucrose with non-caloric sweeteners is an approach to avoid overweight and diabetes development. Non-caloric sweeteners are classified into either artificial as sucralose or natural as stevia. Both of them have been approved by FDA, but the effects of their chronic consumption are controversial. The present study aimed to evaluate the effects of these two sweeteners, in male and female albino mice, on different blood biochemical parameters, enzymes activities and immunological parameters after 8 and 16 weeks of sweeteners administration. 40.5 mg/ml of sucrose, 5.2 mg/ml of sucralose and 4.2 mg/ml of stevia were dissolved individually in distilled water. Mice were administrated by sweetener's solution for 5 h daily. Male and female mice showed a preference for water consumption with sucralose or stevia. Both of the two sweeteners significantly reduced the hemoglobin level, HCT%, RBCs and WBCs count. After 18 weeks, significant elevations in liver and kidney function enzymes were observed in male and female mice administrated with both non-caloric sweeteners. Histopathological examination in sucralose and stevia administrated groups confirmed the biochemical results; where it revealed a severe damage in liver and kidney sections. While, sucrose administration elevated, only, the levels of ALT, AST and cholesterol in male mice. A vigorous elevation in levels of different immunoglobulin (IgG, IgE and IgA) and pro-inflammatory cytokines (IL-6 and -8), that was accompanied by a significant reduction in level of anti-inflammatory cytokine IL-10, was observed in male and female mice groups administrated with sucralose or stevia. On the other hand, sucrose administration led to an elevation in IgA and reduction in IL-10 levels.
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spelling pubmed-75848032020-10-30 The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose Farid, Alyaa Hesham, Marim El-Dewak, Mohamed Amin, Ayman Saudi Pharm J Original Article Replacing sucrose with non-caloric sweeteners is an approach to avoid overweight and diabetes development. Non-caloric sweeteners are classified into either artificial as sucralose or natural as stevia. Both of them have been approved by FDA, but the effects of their chronic consumption are controversial. The present study aimed to evaluate the effects of these two sweeteners, in male and female albino mice, on different blood biochemical parameters, enzymes activities and immunological parameters after 8 and 16 weeks of sweeteners administration. 40.5 mg/ml of sucrose, 5.2 mg/ml of sucralose and 4.2 mg/ml of stevia were dissolved individually in distilled water. Mice were administrated by sweetener's solution for 5 h daily. Male and female mice showed a preference for water consumption with sucralose or stevia. Both of the two sweeteners significantly reduced the hemoglobin level, HCT%, RBCs and WBCs count. After 18 weeks, significant elevations in liver and kidney function enzymes were observed in male and female mice administrated with both non-caloric sweeteners. Histopathological examination in sucralose and stevia administrated groups confirmed the biochemical results; where it revealed a severe damage in liver and kidney sections. While, sucrose administration elevated, only, the levels of ALT, AST and cholesterol in male mice. A vigorous elevation in levels of different immunoglobulin (IgG, IgE and IgA) and pro-inflammatory cytokines (IL-6 and -8), that was accompanied by a significant reduction in level of anti-inflammatory cytokine IL-10, was observed in male and female mice groups administrated with sucralose or stevia. On the other hand, sucrose administration led to an elevation in IgA and reduction in IL-10 levels. Elsevier 2020-10 2020-09-02 /pmc/articles/PMC7584803/ /pubmed/33132722 http://dx.doi.org/10.1016/j.jsps.2020.08.019 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Farid, Alyaa
Hesham, Marim
El-Dewak, Mohamed
Amin, Ayman
The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose
title The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose
title_full The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose
title_fullStr The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose
title_full_unstemmed The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose
title_short The hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose
title_sort hidden hazardous effects of stevia and sucralose consumption in male and female albino mice in comparison to sucrose
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584803/
https://www.ncbi.nlm.nih.gov/pubmed/33132722
http://dx.doi.org/10.1016/j.jsps.2020.08.019
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