Evidence mapPaperPMID 35464439Full record

ArticleFrontiers in immunology2022

D-Mannose Regulates Hepatocyte Lipid Metabolism

Mengyao Hu, Yu Chen, Fan Deng, Bo Chang, Jialiang Luo, Lijun Dong, Xiao Lu, Yi Zhang, Zhengliang Chen, Jia Zhou

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.2field-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

28 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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 1 institution in 1 country.

Mengyao HuDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yu ChenDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Fan DengDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Bo ChangDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Jialiang LuoDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Lijun DongDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Xiao LuDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yi ZhangDepartment of Medical Laboratory, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, China.
Zhengliang ChenDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Jia ZhouDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Southern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the protective properties and mechanisms of D-mannose against hepatic steatosis in experimental alcoholic liver disease (ALD). Drinking-water supplementation of D-mannose significantly attenuated hepatic steatosis in a standard mouse ALD model established by chronic-binge ethanol feeding, especially hepatocyte lipid deposition. This function of D-mannose on lipid accumulation in hepatocytes was also confirmed using ethanol-treated primary mouse hepatocytes (PMHs) with a D-mannose supplement. Meanwhile, D-mannose regulated lipid metabolism by rescuing ethanol-mediated reduction of fatty acid oxidation genes (PPARα, ACOX1, CPT1) and elevation of lipogenic genes (SREBP1c, ACC1, FASN). PI3K/Akt/mTOR signaling pathway was involved in this effect of D-mannose on lipid metabolism since PI3K/Akt/mTOR pathway inhibitors or agonists could abolish this effect in PMHs. Overall, our findings suggest that D-mannose exhibits its anti-steatosis effect in ALD by regulating hepatocyte lipid metabolism

Indexed as

Fatty LiverLiver Diseases, AlcoholicAnimalsCadaverDisease Models, AnimalEthanolHepatocytesLipid MetabolismLipidsMannoseMicePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesEthanolLipidsMannosePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinasesalcoholic liver diseaseD-mannosehepatic steatosishepatocytelipid metabolismPI3K/Akt/mTOR

Identifiers

PMID35464439
PMCPMC9021718
OpenAlexW4226137650

What Socratic 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 Socratic graph.