Evidence map›Paper›PMID 32599649›Full record

ArticleActa physiologica (Oxford, England)2020

Sodium-glucose cotransporter 1 as a sugar taste sensor in mouse tongue.

Keiko Yasumatsu, Tadahiro Ohkuri, Ryusuke Yoshida, Shusuke Iwata, Robert F Margolskee, Yuzo Ninomiya

Open access · greenAbstract read
In one paragraph

Article in Acta physiologica (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 65 citations in OpenAlex.

  1. Pharmaceutical agents targeting KThe journal of physiological sciences : JPS · 2026
    Article
  2. Review
  3. Noncanonical Taste Transduction of Sugars Elicits Responses in a Dedicated Subset of Gustatory Afferent Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  14. Mechanisms and Functions of Sweet Reception in Oral and Extraoral Organs.International journal of molecular sciences · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Keiko YasumatsuTokyo Dental Junior College, Chiyoda-ku, Tokyo, Japan.ORCID 0000-0002-1911-8792
Tadahiro OhkuriSection of Oral Neuroscience, Graduate School of Dental Sciences, Kyushu University, Fukuoka, Japan.
Ryusuke YoshidaSection of Oral Neuroscience, Graduate School of Dental Sciences, Kyushu University, Fukuoka, Japan.
Shusuke IwataDivision of Sensory Physiology and Medical Application Sensing, Research and Development Centre for Five-Sense Devices, Kyushu University, Fukuoka, Japan.
Robert F MargolskeeMonell Chemical Senses Centre, Philadelphia, PA, USA.
Yuzo NinomiyaDivision of Sensory Physiology and Medical Application Sensing, Research and Development Centre for Five-Sense Devices, Kyushu University, Fukuoka, Japan.
Kyushu University · JPMonell Chemical Senses Center · US

Funding

Pathways and genes of sweet taste cellsR01DC014105 · NIDCD · MONELL CHEMICAL SENSES CENTER · PI MARGOLSKEE, ROBERT F. · 2015 to 2019
$1.6M
NIDCD NIH HHS R01 DC014105
6 · The paper itself

Abstract

aimWe investigated potential neuron types that code sugar information and how sodium-glucose cotransporters (SGLTs) and T1Rs are involved.

methodsWhole-nerve recordings in the chorda tympani (CT) and the glossopharyngeal (GL) nerves and single-fibre recordings in the CT were performed in T1R3-KO and wild-type (WT) mice. Behavioural response measurements were conducted in T1R3-KO mice using phlorizin (Phl), a competitive inhibitor of SGLTs.

resultsResults indicated that significant enhancement occurred in responses to sucrose and glucose (Glc) by adding 10 mmol/L NaCl but not in responses to KCl, monopotassium glutamate, citric acid, quinine sulphate, SC45647(SC) or polycose in both CT and GL nerves. These enhancements were abolished by lingual application of Phl. In single-fibre recording, fibres showing maximal response to sucrose could be classified according to responses to SC and Glc with or without 10 mmol/L NaCl in the CT of WT mice, namely, Phl-insensitive type, Phl-sensitive Glc-type and Mixed (Glc and SC responding)-type fibres. In T1R3-KO mice, Phl-insensitive-type fibres disappeared. Results from behavioural experiments showed that the number of licks and amount of intake for Glc with or without 10 mmol/L NaCl were significantly suppressed by Phl.

conclusionWe found evidence for the contribution of SGLTs in sugar sensing in taste cells of mouse tongue. Moreover, we found T1R-dependent (Phl-insensitive) type, Glc-type and Mixed (SGLTs and T1Rs)-type fibres. SGLT1 may be involved in the latter two types and may play important roles in the glucose-specific cephalic phase of digestion and palatable food intake.

Indexed as

SugarsTasteAnimalsMiceMice, Inbred C57BLMice, KnockoutReceptors, G-Protein-CoupledSodium-Glucose Transporter 1TongueReceptors, G-Protein-CoupledSodium-Glucose Transporter 1SugarsglucoseSGLTssugarsweet tasteT1Rstaste

Identifiers

PMID32599649
PMCPMC8284877
OpenAlexW3038284610

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.