Evidence map›Paper›PMID 30669620›Full record

ArticleMolecules (Basel, Switzerland)2019

Effects of Betaine on LPS-Stimulated Activation of Microglial M1/M2 Phenotypes by Suppressing TLR4/NF-κB Pathways in N9 Cells.

Hui Shi, Xiao-Long Wang, Hong-Feng Quan, Lin Yan, Xiu-Ying Pei, Rui Wang, Xiao-Dong Peng

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
6.3field-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

48 citing papers in PubMed, 95 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Foods (Basel, Switzerland) · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. MnTheranostics · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Journal of traditional and complementary medicine · 2022
    Article
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

7 authors at 1 institution in 1 country.

Hui ShiDepartment of Pharmacology, Ningxia Medical University, Yinchuan 750004, China. 15771377892@163.com.
Xiao-Long WangDepartment of Pharmacology, Ningxia Medical University, Yinchuan 750004, China. nomoredrama@126.com.
Hong-Feng QuanDepartment of Pharmacology, Ningxia Medical University, Yinchuan 750004, China. quanhongfeng@163.com.
Lin YanFunctional Experiment Center, School of Basic Medicine, Ningxia Medical University, Yinchuan 750004, China. Yanlin1@Tom.com.
Xiu-Ying PeiLaboratory in Fertility Preservation and Maintenance of Ministry of Education, Ningxia Medical University, Yinchuan 750004, China. peixy@nxmu.edu.cn.
Rui WangDepartment of Pharmacology, Ningxia Medical University, Yinchuan 750004, China. pengxd@nxmu.edu.cn.
Xiao-Dong PengDepartment of Pharmacology, Ningxia Medical University, Yinchuan 750004, China. 11119034@zju.edu.cn.
Ningxia Medical University · CN

Funding

the National Science Foundation of China 81760768
6 · The paper itself

Abstract

Microglia mediate multiple facets of neuroinflammation. They can be phenotypically divided into a classical phenotype (pro-inflammatory, M1) or an alternative phenotype (anti-inflammatory, M2) with different physiological characteristics and biological functions in the inflammatory process. Betaine has been shown to exert anti-inflammatory effects. In this study, we aimed to verify the anti-inflammatory effects of betaine and elucidate its possible molecular mechanisms of action in vitro. Lipopolysaccharide (LPS)-activated microglial cells were used as an inflammatory model to study the anti-inflammatory efficacy of betaine and explore its mechanism of regulating microglial polarisation by investigating the morphological changes and associated inflammatory changes. Cytokine and inflammatory mediator expression was also measured by ELISA, flow cytometry, immunofluorescence, and western blot analysis. Toll-like receptor (TLR)-myeloid differentiation factor 88 (Myd88)-nuclear factor-kappa B (NF-κB) p65, p-NF-κB p65, IκB, p-IκB, IκB kinase (IKK), and p-IKK expression was determined by western blot analysis. Betaine significantly mitigated the production of pro-inflammatory cytokines and increased the release of anti-inflammatory cytokines. It promoted the conversion of the microglia from M1 to M2 phenotype by decreasing the expression of inducible nitric oxide synthase and CD16/32 and by increasing that of CD206 and arginase-1. Betaine treatment inhibited the TLR4/NF-κB pathways by attenuating the expression of TLR4-Myd88 and blocking the phosphorylation of IκB and IKK. In conclusion, betaine could significantly alleviate LPS-induced inflammation by regulating the polarisation of microglial phenotype; thus, it might be an effective therapeutic agent for neurological disorders.

Indexed as

AnimalsBetaineBiomarkersCell LineCell SurvivalCytokinesImmunophenotypingInflammation MediatorsLipopolysaccharidesMicrogliaNF-kappa BNitric OxidePhenotypeSignal TransductionToll-Like Receptor 4BetaineBiomarkersCytokinesInflammation MediatorsLipopolysaccharidesNF-kappa BNitric OxideToll-Like Receptor 4betaineM1/M2 polarisationmicrogliaN9 microglial cellsneuroinflammation

Identifiers

PMID30669620
PMCPMC6359206
OpenAlexW2910361278

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.