Long-Term Consumption of a Sugar-Sweetened Soft Drink in Combination with a Western-Type Diet Is Associated with Morphological and Molecular Changes of Taste Markers Independent of Body Weight Development in Mice.
Barbara LiederJozef ČonkaAgnes T ReinerVictoria ZabelDominik AmeurMark Manuel SomozaKatarina SebekovaPeter CelecVeronika SomozaPublished in: Nutrients (2022)
We investigated whether the long-term intake of a typical sugar-sweetened soft drink (sugar-sweetened beverage, SSB) alters markers for taste function when combined with a standard diet (chow) or a model chow mimicking a Western diet (WD). Adult male CD1 mice had ad libitum access to tap water or SSB in combination with either the chow or the WD for 24 weeks. Energy intake from fluid and food was monitored three times a week. Cardiometabolic markers (body weight and composition, waist circumference, glucose and lipid profile, and blood pressure) were analyzed at the end of the intervention, as was the number and size of the fungiform papillae as well as mRNA levels of genes associated with the different cell types of taste buds and taste receptors in the circumvallate papillae using a cDNA microarray and qPCR. Although the overall energy intake was higher in the WD groups, there was no difference in body weight or other cardiometabolic markers between the SSB and water groups. The chemosensory surface from the fungiform papillae was reduced by 36 ± 19% ( p < 0.05) in the WD group after SSB compared to water intake. In conclusion, the consumption of the SSB reduced the chemosensory surface of the fungiform papillae of CD1 mice when applied in combination with a WD independent of body weight. The data suggest synergistic effects of a high sugar-high fat diet on taste dysfunction, which could further influence food intake and promote a vicious cycle of overeating and taste dysfunction.
Keyphrases
- body weight
- high fat diet
- high fat diet induced
- blood pressure
- physical activity
- weight loss
- insulin resistance
- weight gain
- randomized controlled trial
- oxidative stress
- adipose tissue
- type diabetes
- single cell
- body mass index
- machine learning
- stem cells
- heart rate
- clinical trial
- wild type
- metabolic syndrome
- atomic force microscopy
- single molecule
- big data
- high resolution
- artificial intelligence
- human health