Evidence map›Paper›PMID 38644407›Full record

ArticleMolecular biology reports2024

Dapagliflozin promotes browning of white adipose tissue through the FGFR1-LKB1-AMPK signaling pathway.

Yue Lv, Chengrui Zhao, Qiuyan Jiang, Yilin Rong, Mingfeng Ma, Lili Liang, Weiping Li, Jiuxuan Zhang, Ning Xu, Huiwen Wu

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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  6. The Effects of SGLT2 Inhibitors on Blood Pressure and Other Cardiometabolic Risk Factors.International journal of molecular sciences · 2024 · on this map
    Review
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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

10 authors at 3 institutions in 1 country.

Yue Lv *Science and Technology Center of Fenyang College, Shanxi Medical University, No. 16 Xueyuan Road, Fenyang, Shanxi, 032200, People's Republic of China.
Chengrui Zhao *Science and Technology Center of Fenyang College, Shanxi Medical University, No. 16 Xueyuan Road, Fenyang, Shanxi, 032200, People's Republic of China.
Qiuyan JiangScience and Technology Center of Fenyang College, Shanxi Medical University, No. 16 Xueyuan Road, Fenyang, Shanxi, 032200, People's Republic of China.
Yilin RongScience and Technology Center of Fenyang College, Shanxi Medical University, No. 16 Xueyuan Road, Fenyang, Shanxi, 032200, People's Republic of China.
Mingfeng MaCultivation Key Laboratory of Metabolic Cardiovascular Diseases Research, Fenyang, 032200, People's Republic of China.
Lili LiangCultivation Key Laboratory of Metabolic Cardiovascular Diseases Research, Fenyang, 032200, People's Republic of China.
Weiping LiBasic Sciences Department of Fenyang College, Shanxi Medical University, Fenyang, 032200, People's Republic of China.
Jiuxuan ZhangScience and Technology Center of Fenyang College, Shanxi Medical University, No. 16 Xueyuan Road, Fenyang, Shanxi, 032200, People's Republic of China.
Ning XuDepartment of Oncology, Shanxi Province Fenyang Hospital, Fenyang, 032200, People's Republic of China.
Huiwen WuScience and Technology Center of Fenyang College, Shanxi Medical University, No. 16 Xueyuan Road, Fenyang, Shanxi, 032200, People's Republic of China. huiwenwu@sxmu.edu.cn.
Shanxi Medical University · CNShanxi Fenyang Hospital · CNHuawei Technologies (China) · CN

Funding

Cultivation Key laboratory of Metabolic Cardiovascular Diseases Research grant number TSGJ001This study was supported by the Key Research and Development Project for Introducing High-level Scientific and Technological Talents in Lvliang City grant number 2022RC29
6 · The paper itself

Abstract

backgroundObesity is associated with a wide variety of metabolic disorders that impose significant burdens on patients and society. The "browning" phenomenon in white adipose tissue (WAT) has emerged as a promising therapeutic strategy to combat metabolic disturbances. However, though the anti-diabetic drug dapagliflozin (DAPA) is thought to promote "browning," the specific mechanism of this was previously unclear.

methodsIn this study, C57BL/6 J male mice were used to establish an obesity model by high-fat diet feeding, and 3T3-L1 cells were used to induce mature adipocytes and to explore the role and mechanism of DAPA in "browning" through a combination of in vitro and in vivo experiments.

resultsThe results show that DAPA promotes WAT "browning" and improves metabolic disorders. Furthermore, we discovered that DAPA activated "browning" through the fibroblast growth factor receptors 1-liver kinase B1-adenosine monophosphate-activated protein kinase signaling pathway.

conclusionThese findings provide a rational basis for the use of DAPA in treating obesity by promoting the browning of white adipose tissue.

Indexed as

Adipose Tissue, WhiteBenzhydryl CompoundsGlucosidesProtein Serine-Threonine KinasesReceptor, Fibroblast Growth Factor, Type 1Signal Transduction3T3-L1 CellsAdipocytesAdipose Tissue, BrownAMP-Activated Protein KinasesAnimalsDiet, High-FatMaleMiceMice, Inbred C57BLObesityAMP-Activated Protein KinasesBenzhydryl CompoundsdapagliflozinFgfr1 protein, mouseGlucosidesProtein Serine-Threonine KinasesReceptor, Fibroblast Growth Factor, Type 1Stk11 protein, mouseAMPKDapagliflozinFGFR1LKB1ObesityWhite adipose tissue browning

Identifiers

PMID38644407
PMCPMC11033239
OpenAlexW4394985555

What OpenQuestion holds

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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.