Evidence map›Paper›PMID 37246829›Full record

ArticleHistology and histopathology2023

D-mannose reduces adipogenesis by inhibiting the PI3K/AKT signaling pathway.

Haozhi Lin, Xin Li, Jiping Zhao, Lei Wang, Yizhen Liu, Cui Gao

Abstract read
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In one paragraph

Article in Histology and histopathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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  4. Eugenol inhibits preadipocyte differentiation and lipid accumulation via upregulating ATF3.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 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

6 authors at 1 institution in 1 country.

Haozhi LinDepartment of Stomatology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shan Dong Province, PR China.
Xin LiDepartment of Neurology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shan Dong Province, PR China.
Jiping ZhaoDepartment of Radiology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shan Dong Province, PR China.
Lei WangDepartment of Stomatology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shan Dong Province, PR China.
Yizhen LiuDepartment of Stomatology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shan Dong Province, PR China.
Cui GaoDepartment of Neurology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, Shan Dong Province, PR China. 1358550488@qq.com.
Qingdao University · CN

Funding

Youth Research Fund of Affiliated Hospital of Qingdao University QDFYQN20190028
6 · The paper itself

Abstract

purposeTo explore the effects and potential mechanisms of D-mannose on adipogenic differentiation of two kinds of representative mesenchymal stem cells (MSCs).

methodsWe cultured two kinds of representative MSCs, human adipose tissue-derived stromal cells (hADSCs) as well as human bone marrow mesenchymal stem cells (hBMSCs), with adipogenic-induced medium containing D-mannose or D-fructose as the control. Oil red O staining, quantitative real-time polymerase chain reaction (qRT-PCR), and western blot (WB) were used to detect whether D-mannose had effects on adipogenic differentiation of MSCs. RNA sequencing (RNA-seq) transcriptomic analysis was further used to explore the potential mechanisms of D-mannose on adipogenic differentiation of MSCs. After that, qRT-PCR and WB were used to verify the results of RNA-seq. Last, we removed bilateral ovaries of female rats to establish an estrogen deficiency obesity model, and gave D-mannose intragastric administration. One month later, the femurs of rats were sliced for oil red O staining, and the inhibitory effect of D-mannose on lipid formation in vivo was studied.

resultsOil red O staining, qRT-PCR and WB in vitro demonstrated that D-mannose inhibited the adipogenic differentiation of both hADSCs and hBMSCs. Oil red O staining of femur sections proved that D-mannose was able to reduce in vivo adipogenesis. The results of RNA-seq transcriptomic analysis revealed that the adipogenesis-inhibition effects of D-mannose were performed by antagonizing the PI3K/AKT signaling pathway. Besides, qRT-PCR and WB further verified the results of RNA-seq.

conclusionOur study indicated that D-mannose was able to reduce adipogenic differentiation of both hADSCs and hBMSCs by antagonizing the PI3K/AKT signaling pathway. D-mannose is expected to be a safe and effective treatment strategy for obesity.

Indexed as

AdipogenesisProto-Oncogene Proteins c-aktAnimalsAzo CompoundsCell DifferentiationCells, CulturedFemaleHumansMannoseObesityOsteogenesisPhosphatidylinositol 3-KinasesRatsSignal TransductionAzo CompoundsMannoseoil red OPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-akt

Identifiers

PMID37246829
OpenAlexW4378640534

What OpenQuestion holds

Textmetadata
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.