Evidence map›Paper›PMID 31999787›Full record

ArticlePloS one2020

Hydrocarboxylic acid receptor 1 in BAT regulates glucose uptake in mice fed a high-fat diet.

Eunjin Kwon, Taesik Yoo, Hye-Young Joung, Young-Hwan Jo

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Eunjin KwonDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, Unites States of America.
Taesik YooDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, Unites States of America.
Hye-Young JoungDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, Unites States of America.
Young-Hwan JoDivision of Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, Unites States of America.ORCID 0000-0001-6939-8000
Albert Einstein College of Medicine · US

Funding

Stable Isotope and Metabolomics CoreP60DK020541 · NIDDK · YESHIVA UNIVERSITY · PI FLEISCHER, NORMAN S. · 1986 to 2014
$29.8M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Energy Homeostasis: GABAergic and Non-GABAergic POMC NeuronsR01DK092246 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI JO, YOUNG-HWAN · 2012 to 2021
$3.7M
NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P60 DK020541NIDDK NIH HHS R01 DK092246
6 · The paper itself

Abstract

Interscapular brown adipose tissue (BAT) has the capability to take up glucose from the circulation. Despite the important role of BAT in the control of glucose homeostasis, the metabolic fate and function of glucose in BAT remain elusive as there is clear dissociation between glucose uptake and BAT thermogenesis. Interestingly, intracellular glycolysis and lactate production appear to be required for glucose uptake by BAT. Here, we specifically examine whether activation of lactate receptors in BAT plays a key role in regulating glucose homeostasis in mice fed a high-fat diet (HFD). When C57BL/6J mice are given HFD for 5 weeks at 28°C, male, but not female, mice gain body weight and develop hyperglycemia. Importantly, high-fat feeding upregulates expression of the lactate receptor hydroxycarboxylic acid receptor 1 (HCAR1) in female C57BL/6J mice, whereas male C57BL/6J mice show reduced HCAR1 expression in BAT. Treatment with the HCAR1 agonist lowers systemic glucose levels in male DIO mice. This reduction is associated with increased glucose uptake in BAT. Therefore, our results suggest that HCAR1 in BAT may contribute to the development of hyperglycemia in male C57BL/6J DIO mice.

Indexed as

Adipose Tissue, BrownAnimalsDiet, High-FatDisease Models, AnimalDown-RegulationFemaleGlucoseHyperglycemiaMaleMiceMice, Inbred C57BLObesityReceptors, G-Protein-CoupledSex CharacteristicsUp-RegulationGlucoseHcar1 protein, mouseReceptors, G-Protein-Coupled

Identifiers

PMID31999787
PMCPMC6992197
OpenAlexW3003457076

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.