The Effect of Artificial Sweeteners on Blood Glucose Response
Trial Snapshot
- Phase
- Not Applicable
- Status
- Withdrawn
- Sponsor
- Northumbria University
- Locations
- 2
- Primary Endpoint
- Blood glucose response
Study Overview
Brief Summary
The purpose of this study is to determine whether the presece of the artificial sweeteners aspartame, saccharin and asceulfame-k affect the blood glucose responses to an orally incested glucose solution.
Detailed Description
Sweet taste receptors, similar to those located on the lingual taste buds have been located along in the lining of the gut. Recent studies have demonstrated that activation of these sweetness taste receptors, either by sugars such as glucose, fructose, lactose, or artificial sweeteners such as saccharin and aspartame can influence the way nutrients, including glucose are absorbed from the gut into the bloodstream. Studies in animal models have shown that activation of the sweet taste receptors can increase the expression of the sodium-dependant glucose transporter 1 (SGLT1) and glucose transporter 2 (GLUT2) which transport glucose from the lumen into the bloodstream. Thus providing a potential mechanism by which glucose uptake can be regulated. Although artificial sweeteners stimulate the sweet taste receptors, they have little nutritive value, so that when they are consumed in the absence of any other nutrients there is little effect on blood glucose response. However, the effects of consuming artificial sweeteners in combination with sugars such as glucose is unclear. The purpose of this study is to investigate whether the addition of artificial sweeteners to an orally consumed glucose solution affects the rate at which the glucose appears in the blood.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Basic Science
- Masking
- Double (Participant, Investigator)
Eligibility Criteria
- Ages
- 18 Years to 45 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Healthy subjects
- •Aged 18-45 years
- •BMI (19-25 kg/m2)
- •Weight stable in past 3 months
Exclusion Criteria
- •Females who are pregnant of breastfeeding
- •Regular intake of emdication, other than females taking oral contraceptives
- •Medical illness
- •Gastrointestinal disorders
- •Food allergies
Outcomes
Primary Outcomes
Blood glucose response
Time Frame: 90 min
Blood glucose will be determined at baseline and for 90 min following the consumption of the test drinks
Secondary Outcomes
- Subjective appetite(90 min)
