# Determination of sweetener specificity of horse gut-expressed sweet taste receptor T1R2-T1R3 and its significance for energy provision and hydration

**Authors:** Liberty Smith, Andrew W. Moran, Miran Al-Rammahi, Kristian Daly, Soraya P. Shirazi-Beechey

PMC · DOI: 10.3389/fvets.2024.1325135 · 2024-02-12

## TL;DR

This study identifies which sweeteners activate the sweet taste receptor in horses, which could help improve their glucose absorption and hydration.

## Contribution

The paper reveals the sweetener specificity of the horse sweet taste receptor T1R2-T1R3 for the first time.

## Key findings

- Sucralose, stevia, and neohesperidin dihydrochalcone activate the horse T1R2-T1R3 receptor.
- Cyclamate does not activate the horse T1R2-T1R3 receptor.
- Understanding this specificity can help design dietary additives to enhance glucose absorption and hydration in horses.

## Abstract

Studies carried out in several species have demonstrated that detection of low-calorie sweeteners in the lumen of the intestine, by the sweet receptor, T1R2-T1R3, initiates a signaling pathway leading to enhanced expression and activity of intestinal Na+/glucose cotransporter 1, SGLT1. This results in an increased gut capacity to absorb glucose, sodium chloride and water, the basis for oral rehydration therapy. Horses express T1R2, T1R3 and downstream signaling elements in the intestinal tissue. As such, the potential of sweetener-stimulation of T1R2-T1R3 leading to upregulation of SGLT1 allows the provision of more glucose (energy) and hydration for horses. This is especially important when the need for glucose increases during strenuous exercise, pregnancy, and lactation. There are significant differences among species in the ability to detect sweeteners. Amino acid substitutions and pseudogenization of taste receptor genes underlie these variations. Nothing is known about the sweetener specificity of horse T1R2-T1R3. Using heterologous expression methodology, we demonstrate that sweeteners sucralose, stevia and neohesperidin dihydrochalcone (NHDC) activate horse T1R2-T1R3, but cyclamate does not. Determination of sweetener specificity of equine sweet receptor is crucial for developing suitable dietary additives to optimize glucose absorption, hydration and avoiding the intestinal disease brought about by microbial fermentation of unabsorbed carbohydrate reaching the large intestine.

## Linked entities

- **Genes:** TAS1R2 (taste 1 receptor member 2) [NCBI Gene 80834], TAS1R3 (taste 1 receptor member 3) [NCBI Gene 83756], SLC5A1 (solute carrier family 5 member 1) [NCBI Gene 6523]
- **Chemicals:** sucralose (PubChem CID 71485), stevia (PubChem CID 6918840), neohesperidin dihydrochalcone (PubChem CID 30231), cyclamate (PubChem CID 7533)

## Full-text entities

- **Genes:** SGLT1 [NCBI Gene 100033952]
- **Diseases:** intestinal disease (MESH:D007410)
- **Species:** Equus caballus (domestic horse, species) [taxon 9796]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10894948/full.md

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Source: https://tomesphere.com/paper/PMC10894948