High-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice

Abstract Background Non-caloric artificial sweeteners (NCAS) are widely used as a substitute for dietary sugars to control body weight or glycemia. Paradoxically, some interventional studies in humans and rodents have shown unfavorable changes in glucose homeostasis in response to NCAS consumption....

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Main Authors: Joan Serrano, Kathleen R. Smith, Audra L. Crouch, Vandana Sharma, Fanchao Yi, Veronika Vargova, Traci E. LaMoia, Lydia M. Dupont, Vanida Serna, Fenfen Tang, Laisa Gomes-Dias, Joshua J. Blakeslee, Emmanuel Hatzakis, Scott N. Peterson, Matthew Anderson, Richard E. Pratley, George A. Kyriazis
Format: Article
Language:English
Published: BMC 2021-01-01
Series:Microbiome
Subjects:
Online Access:https://doi.org/10.1186/s40168-020-00976-w
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author Joan Serrano
Kathleen R. Smith
Audra L. Crouch
Vandana Sharma
Fanchao Yi
Veronika Vargova
Traci E. LaMoia
Lydia M. Dupont
Vanida Serna
Fenfen Tang
Laisa Gomes-Dias
Joshua J. Blakeslee
Emmanuel Hatzakis
Scott N. Peterson
Matthew Anderson
Richard E. Pratley
George A. Kyriazis
spellingShingle Joan Serrano
Kathleen R. Smith
Audra L. Crouch
Vandana Sharma
Fanchao Yi
Veronika Vargova
Traci E. LaMoia
Lydia M. Dupont
Vanida Serna
Fenfen Tang
Laisa Gomes-Dias
Joshua J. Blakeslee
Emmanuel Hatzakis
Scott N. Peterson
Matthew Anderson
Richard E. Pratley
George A. Kyriazis
High-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice
Microbiome
Artificial sweeteners
Saccharin
Sweet taste receptors
Gut microbiota
Glucose intolerance
Short-chain fatty acids
author_facet Joan Serrano
Kathleen R. Smith
Audra L. Crouch
Vandana Sharma
Fanchao Yi
Veronika Vargova
Traci E. LaMoia
Lydia M. Dupont
Vanida Serna
Fenfen Tang
Laisa Gomes-Dias
Joshua J. Blakeslee
Emmanuel Hatzakis
Scott N. Peterson
Matthew Anderson
Richard E. Pratley
George A. Kyriazis
author_sort Joan Serrano
title High-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice
title_short High-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice
title_full High-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice
title_fullStr High-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice
title_full_unstemmed High-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice
title_sort high-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and mice
publisher BMC
series Microbiome
issn 2049-2618
publishDate 2021-01-01
description Abstract Background Non-caloric artificial sweeteners (NCAS) are widely used as a substitute for dietary sugars to control body weight or glycemia. Paradoxically, some interventional studies in humans and rodents have shown unfavorable changes in glucose homeostasis in response to NCAS consumption. The causative mechanisms are largely unknown, but adverse changes in gut microbiota have been proposed to mediate these effects. These findings have raised concerns about NCAS safety and called into question their broad use, but further physiological and dietary considerations must be first addressed before these results are generalized. We also reasoned that, since NCAS are bona fide ligands for sweet taste receptors (STRs) expressed in the intestine, some metabolic effects associated with NCAS use could be attributed to a common mechanism involving the host. Results We conducted a double-blind, placebo-controlled, parallel arm study exploring the effects of pure saccharin compound on gut microbiota and glucose tolerance in healthy men and women. Participants were randomized to placebo, saccharin, lactisole (STR inhibitor), or saccharin with lactisole administered in capsules twice daily to achieve the maximum acceptable daily intake for 2 weeks. In parallel, we performed a 10-week study administering pure saccharin at a high dose in the drinking water of chow-fed mice with genetic ablation of STRs (T1R2-KO) and wild-type (WT) littermate controls. In humans and mice, none of the interventions affected glucose or hormonal responses to an oral glucose tolerance test (OGTT) or glucose absorption in mice. Similarly, pure saccharin supplementation did not alter microbial diversity or composition at any taxonomic level in humans and mice alike. No treatment effects were also noted in readouts of microbial activity such as fecal metabolites or short-chain fatty acids (SCFA). However, compared to WT, T1R2-KO mice were protected from age-dependent increases in fecal SCFA and the development of glucose intolerance. Conclusions Short-term saccharin consumption at maximum acceptable levels is not sufficient to alter gut microbiota or induce glucose intolerance in apparently healthy humans and mice. Trial registration Trial registration number NCT03032640 , registered on January 26, 2017. Video abstract
topic Artificial sweeteners
Saccharin
Sweet taste receptors
Gut microbiota
Glucose intolerance
Short-chain fatty acids
url https://doi.org/10.1186/s40168-020-00976-w
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spelling doaj-fd0e743042a248bcaf59acc1822c7f2d2021-01-17T12:55:08ZengBMCMicrobiome2049-26182021-01-019111810.1186/s40168-020-00976-wHigh-dose saccharin supplementation does not induce gut microbiota changes or glucose intolerance in healthy humans and miceJoan Serrano0Kathleen R. Smith1Audra L. Crouch2Vandana Sharma3Fanchao Yi4Veronika Vargova5Traci E. LaMoia6Lydia M. Dupont7Vanida Serna8Fenfen Tang9Laisa Gomes-Dias10Joshua J. Blakeslee11Emmanuel Hatzakis12Scott N. Peterson13Matthew Anderson14Richard E. Pratley15George A. Kyriazis16Department of Biological Chemistry & Pharmacology, College of Medicine, The Ohio State UniversityDepartment of Biological Chemistry & Pharmacology, College of Medicine, The Ohio State UniversityDepartment of Microbiology, College of Arts & Sciences, The Ohio State UniversitySanford Burnham Prebys Medical Discovery InstituteTranslational Research Institute for Metabolism and Diabetes, Advent-HealthTranslational Research Institute for Metabolism and Diabetes, Advent-HealthDepartment of Biological Chemistry & Pharmacology, College of Medicine, The Ohio State UniversityDepartment of Biological Chemistry & Pharmacology, College of Medicine, The Ohio State UniversityDepartment of Biological Chemistry & Pharmacology, College of Medicine, The Ohio State UniversityDepartment of Food Science and Technology, College of Food, Agricultural & Environmental Sciences, The Ohio State UniversityDepartment of Horticulture and Crop Science, College of Food, Agricultural & Environmental Sciences, The Ohio State UniversityDepartment of Horticulture and Crop Science, College of Food, Agricultural & Environmental Sciences, The Ohio State UniversityDepartment of Food Science and Technology, College of Food, Agricultural & Environmental Sciences, The Ohio State UniversitySanford Burnham Prebys Medical Discovery InstituteDepartment of Microbiology, College of Arts & Sciences, The Ohio State UniversityTranslational Research Institute for Metabolism and Diabetes, Advent-HealthDepartment of Biological Chemistry & Pharmacology, College of Medicine, The Ohio State UniversityAbstract Background Non-caloric artificial sweeteners (NCAS) are widely used as a substitute for dietary sugars to control body weight or glycemia. Paradoxically, some interventional studies in humans and rodents have shown unfavorable changes in glucose homeostasis in response to NCAS consumption. The causative mechanisms are largely unknown, but adverse changes in gut microbiota have been proposed to mediate these effects. These findings have raised concerns about NCAS safety and called into question their broad use, but further physiological and dietary considerations must be first addressed before these results are generalized. We also reasoned that, since NCAS are bona fide ligands for sweet taste receptors (STRs) expressed in the intestine, some metabolic effects associated with NCAS use could be attributed to a common mechanism involving the host. Results We conducted a double-blind, placebo-controlled, parallel arm study exploring the effects of pure saccharin compound on gut microbiota and glucose tolerance in healthy men and women. Participants were randomized to placebo, saccharin, lactisole (STR inhibitor), or saccharin with lactisole administered in capsules twice daily to achieve the maximum acceptable daily intake for 2 weeks. In parallel, we performed a 10-week study administering pure saccharin at a high dose in the drinking water of chow-fed mice with genetic ablation of STRs (T1R2-KO) and wild-type (WT) littermate controls. In humans and mice, none of the interventions affected glucose or hormonal responses to an oral glucose tolerance test (OGTT) or glucose absorption in mice. Similarly, pure saccharin supplementation did not alter microbial diversity or composition at any taxonomic level in humans and mice alike. No treatment effects were also noted in readouts of microbial activity such as fecal metabolites or short-chain fatty acids (SCFA). However, compared to WT, T1R2-KO mice were protected from age-dependent increases in fecal SCFA and the development of glucose intolerance. Conclusions Short-term saccharin consumption at maximum acceptable levels is not sufficient to alter gut microbiota or induce glucose intolerance in apparently healthy humans and mice. Trial registration Trial registration number NCT03032640 , registered on January 26, 2017. Video abstracthttps://doi.org/10.1186/s40168-020-00976-wArtificial sweetenersSaccharinSweet taste receptorsGut microbiotaGlucose intoleranceShort-chain fatty acids