Evidence map›Paper›PMID 27089323›Full record

ArticleInternational journal of molecular sciences2016

Regulation of Adipogenesis by Quinine through the ERK/S6 Pathway.

Xiaomin Ning, Jingjing He, Xin'e Shi, Gongshe Yang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  5. Review
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  10. Article
  11. Taste 2 Receptor Is Involved in Differentiation of 3T3-L1 Preadipocytes.International journal of molecular sciences · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. An update on extra-oral bitter taste receptors.Journal of translational medicine · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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.

Xiaomin NingLaboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest Agriculture and Forestry University, Yangling 712100, China. xmning@hotmail.com.
Jingjing HeLaboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest Agriculture and Forestry University, Yangling 712100, China. wsjj1987@hotmail.com.
Xin'e ShiLaboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest Agriculture and Forestry University, Yangling 712100, China. xineshi@163.com.
Gongshe YangLaboratory of Animal Fat Deposition and Muscle Development, College of Animal Science and Technology, Northwest Agriculture and Forestry University, Yangling 712100, China. gsyang999@hotmail.com.
Northwest A&F University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quinine is a bitter tasting compound that is involved in the regulation of body weight as demonstrated in in vivo animal models and in vitro models of the adipogenic system. Arguments exist over the positive or negative roles of quinine in both in vivo animal models and in vitro cell models, which motivates us to further investigate the functions of quinine in the in vitro adipogenic system. To clarify the regulatory functions of quinine in adipogenesis, mouse primary preadipocytes were induced for differentiation with quinine supplementation. The results showed that quinine enhanced adipogenesis in a dose dependent manner without affecting lipolysis. The pro-adipogenic effect of quinine was specific, as other bitter tasting agonists had no effect on adipogenesis. Moreover, the pro-adipogenic effect of quinine was mediated by activation of ERK/S6 (extracellular-signal-regulated kinase/Ribosomal protein S6) signaling. Knockdown of bitter taste receptor T2R106 (taste receptor, type 2, member 106) impaired the pro-adipogenic effect of quinine and suppressed the activation of ERK/S6 signaling. Taken together, quinine stimulates adipogenesis through ERK/S6 signaling, which at least partly functions via T2R106.

Indexed as

3T3-L1 CellsAdipocytesAdipogenesisAnimalsCell DifferentiationDose-Response Relationship, DrugExtracellular Signal-Regulated MAP KinasesGene Expression RegulationMAP Kinase Signaling SystemMiceQuinineReceptors, G-Protein-CoupledRibosomal Protein S6Extracellular Signal-Regulated MAP KinasesQuinineReceptors, G-Protein-CoupledRibosomal Protein S6ribosomal protein S6, mouseTas2R108 protein, mouseadipogenesisERK/S6 signalingquinineT2R106

Identifiers

PMID27089323
PMCPMC4848960
OpenAlexW2338718377

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.