Evidence map›Paper›PMID 24150604›Full record

ArticleDiabetes2014

Irisin stimulates browning of white adipocytes through mitogen-activated protein kinase p38 MAP kinase and ERK MAP kinase signaling.

Yuan Zhang, Rui Li, Yan Meng, Shiwu Li, William Donelan, Yan Zhao, Lei Qi, Mingxiang Zhang, Xingli Wang, Taixing Cui and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 351 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
351citing papers in PubMed, 2 pooled it
27.7field-weighted citation impact, top 1% 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

351 citing papers in PubMed, 2 syntheses or guidelines pooled it, 719 citations in OpenAlex.

  1. Protective role of irisin on bone in osteoporosis: a systematic review of rodent studies.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
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  17. Advances in research on thermogenic substances.Journal of physiological anthropology · 2026
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291 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Yuan ZhangCenter for Stem Cell and Regenerative Medicine, The Second Hospital of Shandong University, Jinan, People's Republic of China.
Rui Li
Yan Meng
Shiwu Li
William Donelan
Yan Zhao
Lei Qi
Mingxiang Zhang
Xingli Wang
Taixing Cui
Li-Jun Yang
Dongqi Tang
Qilu Hospital of Shandong University · CNSecond Hospital of Shandong University · CNUniversity of Florida · US

Funding

Reveresal of Diabetes by Pdx1-VP16 and Pax4-Induced Islet RegenerationK01DK080884 · NIDDK · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI TANG, DONGQI DQ · 2008 to 2012
$602k
NIDDK NIH HHS K01 DK080884
6 · The paper itself

Abstract

The number and activity of brown adipocytes are linked to the ability of mammals to resist body fat accumulation. In some conditions, certain white adipose tissue (WAT) depots are readily convertible to a ''brown-like'' state, which is associated with weight loss. Irisin, a newly identified hormone, is secreted by skeletal muscles into circulation and promotes WAT "browning" with unknown mechanisms. In the current study, we demonstrated in mice that recombinant irisin decreased the body weight and improved glucose homeostasis. We further showed that irisin upregulated uncoupling protein-1 (UCP-1; a regulator of thermogenic capability of brown fat) expression. This effect was possibly mediated by irisin-induced phosphorylation of the p38 mitogen-activated protein kinase (p38 MAPK) and extracellular signal-related kinase (ERK) signaling pathways. Inhibition of the p38 MAPK by SB203580 and ERK by U0126 abolished the upregulatory effect of irisin on UCP-1. In addition, irisin also promoted the expression of betatrophin, another newly identified hormone that promotes pancreatic β-cell proliferation and improves glucose tolerance. In summary, our data suggest that irisin can potentially prevent obesity and associated type 2 diabetes by stimulating expression of WAT browning-specific genes via the p38 MAPK and ERK pathways.

Indexed as

3T3-L1 CellsAdipocytesAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsButadienesCaenorhabditis elegans ProteinsDietary FatsExtracellular Signal-Regulated MAP KinasesFibronectinsImidazolesMaleMAP Kinase Signaling SystemMembrane Transport ProteinsMiceMice, Inbred C57BLButadienesCaenorhabditis elegans ProteinsDietary FatsExtracellular Signal-Regulated MAP KinasesFibronectinsFNDC5 protein, humanImidazolesMembrane Transport ProteinsMitochondrial Uncoupling ProteinsNitrilesp38 Mitogen-Activated Protein KinasesPyridinesRecombinant ProteinsSB 203580U 0126UCP-4 protein, C elegans

Identifiers

PMID24150604
PMCPMC13117908
OpenAlexW2121921343

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.