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Frontiers in veterinary science2024; 11; 1325135; doi: 10.3389/fvets.2024.1325135

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

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.
Publication Date: 2024-02-12 PubMed ID: 38410741PubMed Central: PMC10894948DOI: 10.3389/fvets.2024.1325135Google Scholar: Lookup
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  • Journal Article

Summary

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The researchers found that in horses, certain sweeteners stimulate a particular receptor in the gut which in turn enhances glucose absorption and hydration. This is especially significant for energy provision during demanding periods such as strenuous exercise, pregnancy, and lactation. The sweeteners sucralose, stevia, and NHDC are observed to activate this receptor, whereas cyclamate does not.

Objective of the Research

  • The objective of the research was to determine the extent to which different sweeteners affect the T1R2-T1R3 taste receptors in horse intestines, which have been observed to signal for increase in absorption of glucose, sodium chloride, and water when stimulated.
  • The study’s focus on horses arises from their expression of T1R2, T1R3, and related signaling elements in their intestinal tissue, which, when triggered, could enhance the animal’s energy provision and hydration, particularly crucial during strenuous activities, pregnancy, and lactation.

Amino Acid Substitutions and Pseudogenization

  • The capability of various species to detect sweeteners widely differs due to amino acid substitutions and pseudogenization of taste receptor genes.
  • Such genetic variances underline the importance of understanding each species’ specific reactions to different sweeteners, as applied in this study to horses.

Findings and Results

  • Through an experimental process called heterologous expression, the research identified that the sweeteners sucralose, stevia, and neohesperidin dihydrochalcone (NHDC) are capable of activating horse T1R2-T1R3 receptors. In contrast, the sweetener cyclamate was unable to do this.
  • Identifying these successful agent stimulants is a critical step in developing suitable dietary additives to enhance glucose absorption and hydration in horses and minimizing risks of intestinal disease caused by microbial fermentation of unabsorbed carbohydrates in the large intestine.

Cite This Article

APA
Smith L, Moran AW, Al-Rammahi M, Daly K, Shirazi-Beechey SP. (2024). Determination of sweetener specificity of horse gut-expressed sweet taste receptor T1R2-T1R3 and its significance for energy provision and hydration. Front Vet Sci, 11, 1325135. https://doi.org/10.3389/fvets.2024.1325135

Publication

ISSN: 2297-1769
NlmUniqueID: 101666658
Country: Switzerland
Language: English
Volume: 11
Pages: 1325135

Researcher Affiliations

Smith, Liberty
  • Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Moran, Andrew W
  • Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Al-Rammahi, Miran
  • Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
  • Department of Physiology, Biochemistry and Pharmacology, College of Veterinary Medicine, University of Al-Qadisiyah, Al-Diwaniyah, Iraq.
Daly, Kristian
  • Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Shirazi-Beechey, Soraya P
  • Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.

Conflict of Interest Statement

The authors declare that the research was performed without any commercial or financial interests and as such there is no conflict of interest.

Citations

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