Evidence map›Paper›PMID 26751695›Full record

ArticlePloS one2016

Protection against Experimental Stroke by Ganglioside GM1 Is Associated with the Inhibition of Autophagy.

Li Li, Jinghua Tian, Mitchell King-Wei Long, Yong Chen, Jianfei Lu, Changman Zhou, Tianlong Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
7.2field-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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Ganglioside GM1 and the Central Nervous System.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Gangliosides and Neuroblastomas.International journal of molecular sciences · 2020
    Review
  20. 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 5 institutions in 2 countries.

Li LiDepartment of Anesthesiology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Jinghua TianDepartment of Anatomy, Heze Medical College, Shandong, China.
Mitchell King-Wei LongOsteopathic Medicine, Des Moines University, Des Moines, Iowa, United States of America.
Yong ChenDepartment of Neurology, People's hospital of Deyang City, Sichuan, China.
Jianfei LuDepartment of Anatomy & Histology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Changman ZhouDepartment of Anatomy & Histology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Tianlong WangDepartment of Anesthesiology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Capital Medical University · CNPeking University · CNDes Moines University Osteopathic Medical Center · USDeyang Stomatological Hospital · CNHeze Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledGanglioside GM1, which is particularly abundant in the central nervous system (CNS), is closely associated with the protection against several CNS disorders. However, controversial findings have been reported on the role of GM1 following ischemic stroke. In the present study, using a rat middle cerebral artery occlusion (MCAO) model, we investigated whether GM1 can protect against ischemic brain injury and whether it targets the autophagy pathway. GM1 was delivered to Sprague-Dawley male rats at 3 doses (25 mg/kg, 50 mg/kg, 100 mg/kg) by intraperitoneal injection soon after reperfusion and then once daily for 2 days. The same volume of saline was given as a control. Tat-Beclin-1, a specific autophagy inducer, was administered by intraperitoneal injection at 24 and 48 hours post-MCAO. Infarction volume, mortality and neurological function were assessed at 72 hours after ischemic insult. Immunofluorescence and Western blotting were performed to determine the expression of autophagy-related proteins P62, LC3 and Beclin-1 in the penumbra area. No significant changes in mortality and physiological variables (heart rate, blood glucose levels and arterial blood gases) were observed between the different groups. However, MCAO resulted in enhanced conversion of LC3-I into LC3-II, P62 degradation, high levels of Beclin-1, a large area infarction (26.3±3.6%) and serious neurobehavioral deficits. GM1 (50 mg/kg) treatment significantly reduced the autophagy activation, neurobehavioral dysfunctions, and infarction volume (from 26.3% to 19.5%) without causing significant adverse side effects. However, this biological function could be abolished by Tat-Beclin-1. IN

conclusionGM1 demonstrated safe and robust neuroprotective effects that are associated with the inhibition of autophagy following experimental stroke.

Indexed as

AnimalsApoptosis Regulatory ProteinsAutophagyBeclin-1BrainBrain IschemiaDisease Models, AnimalDrug Administration ScheduleGene Expression RegulationGene Products, tatG(M1) GangliosideHeat-Shock ProteinsInfarction, Middle Cerebral ArteryInjections, IntraperitonealMaleMicrotubule-Associated ProteinsAnxa3 protein, ratApoptosis Regulatory ProteinsBeclin-1Becn1 protein, ratGene Products, tatG(M1) GangliosideHeat-Shock ProteinsMicrotubule-Associated ProteinsNeuroprotective AgentsRecombinant Fusion ProteinsSequestosome-1 ProteinSqstm1 protein, rat

Identifiers

PMID26751695
PMCPMC4709082
OpenAlexW2236292981

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.