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Low intake of digestible carbohydrates ameliorates duodenal absorption of carbohydrates in mice with glucose metabolism disorders induced by artificial sweeteners.

Journal of the science of food and agriculture
August 30, 2019
Qing Shi et al. (6 authors)
Journal ArticleAnimal Study
Study Details

Study Goal

The researchers aimed to evaluate whether a low digestible carbohydrate (LDC) diet could mitigate glucose metabolism disorders induced by prolonged consumption of artificial sweeteners (acesulfame potassium or saccharin) in mice.

Results Summary

Prolonged artificial sweetener consumption led to glucose intolerance, insulin resistance, and altered carbohydrate absorption, but an LDC diet improved these metabolic dysfunctions by modulating sweet taste receptors and glucose transporters.

Population

Mice

Effective Dosage

Not specified

Duration

12 weeks (artificial sweetener administration) + 6 weeks (LDC diet intervention)

Interactions

None mentioned

Extracted Claims (12)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Long-term artificial sweetener consumption
increase
glucose intolerance
-
-
induce
#1
acesulfame potassium (AK) or saccharin (SAC)
increase
metabolic dysfunction
mice
-
led to
#2
Prolonged administration of artificial sweeteners
increase
plasma glucose
mice
-
significantly increased
#3
Prolonged administration of artificial sweeteners
increase
insulin resistance
mice
-
increased
#4
Prolonged administration of artificial sweeteners
increase
sweet taste receptors
mice
-
increased
#5
Prolonged administration of artificial sweeteners
increase
glucose transporters
mice
-
increased
#6
Prolonged administration of artificial sweeteners
increase
absorption of carbohydrates
mice
-
increased
#7
low digestible carbohydrate (LDC) diet
decrease
these altered parameters
mice
-
positively modulated
#8
low digestible carbohydrate (LDC) diet
decrease
detrimental changes associated with artificial sweeteners
mice
-
suggesting overall beneficial effects
#9
Reducing digestible carbohydrates in the diet
decrease
absorption of carbohydrates
-
-
can significantly reduce
#10
Reducing digestible carbohydrates in the diet
decrease
glucose metabolism disorders caused by dietary factors
-
-
improve
#11
reducing the amount of digestible carbohydrates in the feed
decrease
number of intestinal sweet receptors induced by exposure to artificial sweeteners
-
-
can reduce
#12
Abstract

BACKGROUND: Long-term artificial sweetener consumption has been reported to induce glucose intolerance, and the intestinal microbiota seems as an important target. While the impacts of artificial sweeteners on energy balance remain controversial, this work aimed to evaluate the protective effects in mice of a low digestible carbohydrate (LDC) diet on plasma glucose, plasma fasting insulin, sweet taste receptors, glucose transporters, and absorption of carbohydrates, together with consumption of acesulfame potassium (AK) or saccharin (SAC). RESULTS: Artificial sweetener was administered to mice for 12 weeks to induce glucose metabolism disorders; mice were treated with an LDC diet for the final 6 weeks. The experimental groups were treated with an LDC diet that had the same energy as the normal-diet group. Prolonged administration of artificial sweeteners led to metabolic dysfunction, characterized by significantly increased plasma glucose, insulin resistance, sweet taste receptors, glucose transporters, and absorption of carbohydrates. Treatment with an LDC diet positively modulated these altered parameters, suggesting overall beneficial effects of an LDC diet on detrimental changes associated with artificial sweeteners. CONCLUSIONS: Reducing digestible carbohydrates in the diet can significantly reduce the absorption of carbohydrates and improve glucose metabolism disorders caused by dietary factors. These effects may be due to the fact that reducing the amount of digestible carbohydrates in the feed can reduce the number of intestinal sweet receptors induced by exposure to artificial sweeteners. © 2019 Society of Chemical Industry.

Medical Subject Headings (MeSH)
AnimalsBlood GlucoseDiet, Carbohydrate-RestrictedDietary CarbohydratesDigestionDuodenumGastrointestinal MicrobiomeGlucose IntoleranceGlucose Metabolism DisordersInsulinInsulin ResistanceIntestinal AbsorptionMaleMiceMice, Inbred ICRReceptors, G-Protein-CoupledSweetening AgentsTasteWeight Gain
Study Links
Quality Scores
Safety30
Efficacy75/10
Quality65/10
Citation Metrics
Total Citations10
Citations/Year1.7
Relative Citation Ratio0.65
NIH Percentile35.1%
Research Impact Scores
APT Score0.25
Weight Score1.43
Normalized Score0.55
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