Evidence map›Paper›PMID 33976180›Full record

ArticleNature communications2021

Peripheral-specific Y1 receptor antagonism increases thermogenesis and protects against diet-induced obesity.

Chenxu Yan, Tianshu Zeng, Kailun Lee, Max Nobis, Kim Loh, Luoning Gou, Zefeng Xia, Zhongmin Gao, Mohammed Bensellam, Will Hughes and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. 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
5.5field-weighted citation impact, top 3% 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, 57 citations in OpenAlex.

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  7. MTCH2 Suppresses Thermogenesis by Regulating Autophagy in Adipose Tissue.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

22 authors at 4 institutions in 4 countries.

Chenxu Yan *Neuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Tianshu Zeng *Wuhan Union Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Kailun Lee *Neuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.ORCID 0000-0002-0388-2235
Max NobisInvasion and Metastasis Lab, Cancer Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Kim LohNeuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Luoning GouWuhan Union Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Zefeng XiaWuhan Union Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Zhongmin GaoDiabetes and Metabolism Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Mohammed BensellamDiabetes and Metabolism Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.ORCID 0000-0002-1641-1694
Will HughesDiabetes and Metabolism Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Jackie LauNeuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Lei ZhangNeuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.ORCID 0000-0002-3927-8881
Chi Kin IpNeuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.ORCID 0000-0002-0464-4706
Ronaldo EnriquezNeuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Hanyu GaoDiabetes and Metabolism Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Qiao-Ping WangSchool of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Guangzhou, China.
Qi WuDiabetes and Metabolism Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Jody J HaighResearch Institute in Oncology and Hematology, Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, MB, Canada.
D Ross LaybuttDiabetes and Metabolism Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Paul TimpsonInvasion and Metastasis Lab, Cancer Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.
Herbert HerzogNeuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia. h.herzog@garvan.org.au.ORCID 0000-0002-1713-1029
Yan-Chuan ShiNeuroscience Division, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia. y.shi@garvan.org.au.ORCID 0000-0002-8368-6735
Garvan Institute of Medical Research · AUWuhan Union Hospital · CNResearch Institute in Oncology and Hematology · CASun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is caused by an imbalance between food intake and energy expenditure (EE). Here we identify a conserved pathway that links signalling through peripheral Y1 receptors (Y1R) to the control of EE. Selective antagonism of peripheral Y1R, via the non-brain penetrable antagonist BIBO3304, leads to a significant reduction in body weight gain due to enhanced EE thereby reducing fat mass. Specifically thermogenesis in brown adipose tissue (BAT) due to elevated UCP1 is enhanced accompanied by extensive browning of white adipose tissue both in mice and humans. Importantly, selective ablation of Y1R from adipocytes protects against diet-induced obesity. Furthermore, peripheral specific Y1R antagonism also improves glucose homeostasis mainly driven by dynamic changes in Akt activity in BAT. Together, these data suggest that selective peripheral only Y1R antagonism via BIBO3304, or a functional analogue, could be developed as a safer and more effective treatment option to mitigate diet-induced obesity.

Indexed as

AdipocytesAdipose Tissue, BrownAdultAnimalsArginineBiopsyCells, CulturedDiet, High-FatDisease Models, AnimalEnergy MetabolismFemaleHumansMaleMiceMiddle AgedObesityArginineBIBO 3304neuropeptide Y-Y1 receptorNpy1r protein, mouseReceptors, Neuropeptide Y

Identifiers

PMID33976180
PMCPMC8113522
OpenAlexW3163061793

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.