Evidence map›Paper›PMID 28228044›Full record

ArticlePharmaceutical biology2017

Withaferin A protects against spinal cord injury by inhibiting apoptosis and inflammation in mice.

Xianlei Yan, Guangxiang Huang, Quan Liu, Jiemin Zheng, Hongmou Chen, Qidan Huang, Jiakang Chen, Heqing Huang

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.9field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. A Novel Ashwagandha (Biomolecules · 2025
    Article
  3. Review
  4. Neurotrophic Natural Products.Progress in the chemistry of organic natural products · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. ΔMolecules (Basel, Switzerland) · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. 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

8 authors at 2 institutions in 1 country.

Xianlei Yana Department of Neurosurgery , the Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Guangxiang Huangb Department of Neurosurgery , The First Affiliated Hospital of Guangxi Medical University , Nanning , China.
Quan Liua Department of Neurosurgery , the Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Jiemin Zhenga Department of Neurosurgery , the Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Hongmou Chena Department of Neurosurgery , the Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Qidan Huanga Department of Neurosurgery , the Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Jiakang Chena Department of Neurosurgery , the Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Heqing Huanga Department of Neurosurgery , the Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Fourth Affiliated Hospital of Guangxi Medical University · CNGuangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextWithaferin A (WFA) exhibits diverse pharmaceutical applications on human diseases, including rheumatoid arthritis, cancers and microbial infection.

objectiveWe evaluated the neuroprotective role of WFA using a mouse model of spinal cord injury (SCI). MATERIALS AND

methodsBALB/c mice were administrated 10 mg/kg of WFA. Gene expression was measured by real-time PCR, western blot and immunohistochemistry. Cell morphology and apoptosis were determined by H&E staining and TUNEL assay. Motor function was evaluated by the BBB functional scale for continuous 7 weeks.

resultsWFA significantly improved neurobehavioural function and alleviated histological alteration of spinal cord tissues in traumatized mice. Brain-derived neurotrophic factor (BDNF) and glial cell line-derived neurotrophic factor (GDNF) significantly increased in WFA-treated mice. Meanwhile, the expression of Nogo-A and RhoA remarkably decreased in the presence of WFA. Furthermore, the apoptotic cell death was attenuated in mice treated with WFA (31.48 ± 2.50% vs. 50.08 ± 2.08%) accompanied by decreased bax and increased bcl-2. In addition, WFA decreased the expression of pro-inflammatory mediators such as IL-1β (11.20 ± 1.96 ng/mL vs. 17.59 ± 1.42 ng/mL) and TNF-α (57.38 ± 3.57 pg/mL vs. 95.06 ± 9.13 pg/mL). The anti-inflammatory cytokines including TGF-β1 (14.32 ± 1.04 pg/mL vs. 9.37 ± 1.17 pg/mL) and IL-10 (116.80 ± 6.91 pg/mL vs. 72.33 ± 9.35 pg/mL) were elevated after WFA administration. DISCUSSION AND

conclusionThis study demonstrated that WFA has a neuroprotective role by inhibition of apoptosis and inflammation after SCI in mice.

Indexed as

AnimalsAnti-Inflammatory AgentsApoptosisApoptosis Regulatory ProteinsBehavior, AnimalBrain-Derived Neurotrophic FactorDisease Models, AnimalGlial Cell Line-Derived Neurotrophic FactorInflammationInflammation MediatorsMice, Inbred BALB CMotor ActivityNeuroprotective AgentsNogo ProteinsrhoA GTP-Binding Proteinrho GTP-Binding ProteinsAnti-Inflammatory AgentsApoptosis Regulatory ProteinsBrain-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic FactorInflammation MediatorsNeuroprotective AgentsNogo ProteinsrhoA GTP-Binding ProteinRhoA protein, mouserho GTP-Binding ProteinsRtn4 protein, mousewithaferin AWithanolidesanti-inflammatory cytokineCentral nervous systemnatural productpro-inflammatory cytokine

Identifiers

PMID28228044
PMCPMC6130570
OpenAlexW2591160303

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.