Expression of sweet receptor components in equine small intestine: relevance to intestinal glucose transport
Abstract
The heteromeric sweet taste receptor T1R2-T1R3 is expressed on the luminal membrane of certain populations of enteroendocrine cells. Sensing of sugars and other sweet compounds by this receptor activates a pathway in enteroendocrine cells, resulting in secretion of a number of gut hormones, including glucagon-like peptide 2 (GLP-2). This subsequently leads to upregulation in the expression of intestinal Na+/glucose cotransporter, SGLT1, and increased intestinal glucose absorption. On the basis of the current information available on the horse genome sequence, it has been proposed that the gene for T1R2 ( Tas1R2) is absent in the horse. We show here, however, that horses express both the mRNA and protein for T1R2. Equine T1R2 is most closely homologous to that in the pig and the cow. T1R2 protein, along with T1R3, α-gustducin, and GLP-2 proteins are coexpressed in equine intestinal endocrine cells. Intravenous administration of GLP-2, in rats and pigs, leads to an increase in the expression of SGLT1 in absorptive enterocytes and enhancement in blood glucose concentrations. GLP-2 receptor is expressed in enteric neurons, excluding the direct effect of GLP-2 on enterocytes. However, electric stimulation of enteric neurons generates a neural response leading to SGLT1 upregulation, suggesting that sugar in the intestine activates a reflex increase in the functional expression of SGLT1. Horses possess the ability to upregulate SGLT1 expression in response to increased dietary carbohydrates, and to enhance the capacity of the gut to absorb glucose. The gut sweet receptor provides an accessible target for manipulating the equine gut to absorb glucose (and water), allowing greater energy uptake and hydration for hard-working horses.
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GLP-2 release is STR-dependent in rodents and inhibited by gurmarin.
“This is also true for GLP-2 release, which is STR-dependent in rodents (28,29) and inhibited by the murine STR inhibitor, gurmarin (30).”
From Gut mechanisms linking intestinal sweet sensing to glycemic control (2018) · cites this paper as [30]
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- Authors
- Daly, K., Al-Rammahi, M., Arora, D. K., Moran, A. W., Proudman, C. J., Ninomiya, Y., & Shirazi-Beechey, S. P.
- Affiliations
- University of Liverpool (GB)
- Kyushu University (JP)
- Epithelial Function and Development Group, Department of Functional and Comparative Genomics, Institute of Integrative Biology, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, United Kingdom;
- Venue
- American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
- Publisher
- American Physiological Society
- Published
- 2012-07-15
- Volume
- 303
- Issue
- 2
- Pages
- R199-R208
- ISSN
- 0363-6119 (ISSN-L)
- 1522-1490
- OpenAlex
- W2096728081
- Cited by
- 70
- References
- 51
- Citations by year
- 2025: 5 · 2024: 4 · 2023: 3 · 2022: 4 · 2021: 3 · 2020: 5 · 2019: 5 · 2018: 6 · 2017: 4 · 2016: 6 · 2015: 7 · 2014: 7 · 2013: 7 · 2012: 4
- FWCI
- 7.44
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Regulatory, Integrative and Comparative Physiology (publishedVersion)
- PubMed (publishedVersion)
- Surrey Research Insight Open Access (The University of Surrey) (submittedVersion)
- Funders
- University of Pennsylvania
- Horserace Betting Levy Board
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Biochemical Analysis and Sensing Techniques
- Health Sciences › Veterinary › Equine › Veterinary Equine Medical Research
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- sweet taste receptor, T1R2, T1R3, equine small intestine, intestinal glucose absorption, SGLT1, glucagon-like peptide-2, enteroendocrine cells, alpha-gustducin, enteric neurons, gastrointestinal hormones, horses, dietary carbohydrates, hydration
- MeSH terms
- Amino Acid Sequence, Animals, Biological Transport, Cats, Dietary Carbohydrates, Energy Metabolism, Epithelial Cells, Female, Glucose, Horses, Intestine, Small, Male, Molecular Sequence Data, Swine, Tongue, Transducin, Enteroendocrine Cells, Receptors, G-Protein-Coupled, Sodium-Glucose Transporter 1, Glucagon-Like Peptide 2
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