Evidence map›Paper›PMID 37321837›Full record

ArticleCell proliferation2024

Decreased YB-1 expression denervates brown adipose tissue and contributes to age-related metabolic dysfunction.

Ruoyu Zhou, Yan Huang, Xu Feng, Rui Zhou, Liwen Wang, Genqing Xie, Yuan Xiao, Haiyan Zhou

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Article
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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

8 authors at 2 institutions in 1 country.

Ruoyu ZhouDepartment of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
Yan HuangDepartment of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
Xu FengDepartment of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
Rui ZhouDepartment of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
Liwen WangDepartment of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
Genqing XieDepartment of Endocrinology, The First People's Hospital of Xiangtan city, Xiangtan, China.
Yuan XiaoDepartment of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
Haiyan ZhouDepartment of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.ORCID https://orcid.org/0000-0002-0868-3606
Central South University · CNXiangshan County First People's Hospital · CN

Funding

China Postdoctoral Science Foundation 2022M713514National Natural Science Foundation of China 82000811National Natural Science Foundation of China 82170866Natural Science Foundation of Hunan Province, China 2020JJ4593Natural Science Foundation of Hunan Province, China 2022JJ30990Natural Science Foundation of Hunan Province, China 2023JJ30890
6 · The paper itself

Abstract

Thermogenesis in brown adipose tissue (BAT) declines with aging, however, the underlying mechanism remains unclear. Here, we show that the expression of Y-box binding protein 1 (YB-1), a critical DNA/RNA binding protein, decreased in the BAT of aged mice due to the reduction of microbial metabolite butyrate. Genetic ablation of YB-1 in the BAT accelerated diet-induced obesity and BAT thermogenic dysfunction. In contrast, overexpression of YB-1 in the BAT of aged mice was sufficient to promote BAT thermogenesis, thus alleviating diet-induced obesity and insulin resistance. Interestingly, YB-1 had no direct effect on adipose UCP1 expression. Instead, YB-1 promoted axon guidance of BAT via regulating the expression of Slit2, thus potentiating sympathetic innervation and thermogenesis. Moreover, we have identified that a natural compound Sciadopitysin, which promotes YB-1 protein stability and nuclear translocation, alleviated BAT aging and metabolic disorders. Together, we reveal a novel fat-sympathetic nerve unit in regulating BAT senescence and provide a promising strategy against age-related metabolic disorders.

Indexed as

Adipose Tissue, BrownInsulin ResistanceAnimalsDietMiceMice, Inbred C57BLObesityThermogenesisTranscription FactorsTranscription FactorsYbx1 protein, mouse

Identifiers

PMID37321837
PMCPMC10771110
OpenAlexW4380853646

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.