Evidence map›Paper›PMID 28195036›Full record

ArticleCell transplantation2017

GSK-3β Inhibition Induced Neuroprotection, Regeneration, and Functional Recovery After Intracerebral Hemorrhagic Stroke.

Yingying Zhao, Zheng Zachory Wei, James Ya Zhang, Yongbo Zhang, Soonmi Won, Jinmei Sun, Shan Ping Yu, Jimei Li, Ling Wei

Open access · goldAbstract read
In one paragraph

Article in Cell transplantation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Systematic Understanding of Mechanism of Yi-Qi-Huo-Xue Decoction Against Intracerebral Hemorrhagic Stroke Using a Network Pharmacology Approach.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  18. Article
  19. 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

9 authors at 3 institutions in 2 countries.

Yingying Zhao
Zheng Zachory Wei
James Ya Zhang
Yongbo Zhang
Soonmi Won
Jinmei Sun
Shan Ping Yu
Jimei Li
Ling Wei
Emory University · USCapital Medical University · CNBeijing Friendship Hospital · CN

Funding

Application of optogenetics in iPS cell transplantation therapy for ischemic stroR01NS085568 · NINDS · EMORY UNIVERSITY · PI GROSS, ROBERT E, WEI, LING · 2014 to 2018
$1.7M
Stem cell transplantation therapy via intranasal delivery after strokeR01NS091585 · NINDS · EMORY UNIVERSITY · PI WEI, LING · 2016 to 2020
$1.7M
Transplantation of Pre-conditioned Bone Marrow Mesenchymal Stem Cells after IscheR01NS062097 · NINDS · EMORY UNIVERSITY · PI WEI, LING · 2010 to 2014
$1.7M
Protection of the Brain by Chemical HypothermiaI01RX000666 · VA · VETERANS HEALTH ADMINISTRATION · PI YU, SHAN P. · 2015 to 2016
–
NINDS NIH HHS R01 NS062097NINDS NIH HHS R01 NS085568NINDS NIH HHS R01 NS091585RRD VA I01 RX000666
6 · The paper itself

Abstract

Hemorrhagic stroke is a devastating disease that lacks effective therapies. In the present investigation, we tested 6-bromoindirubin-3'-oxime (BIO) as a selective glycogen synthase kinase-3β (GSK-3β) inhibitor in a mouse model of intracerebral hemorrhage (ICH). ICH was induced by injection of collagenase IV into the striatum of 8- to 10-week-old C57BL/6 mice. BIO (8 μg/kg, IP) was administered following either an acute delivery (0-2 h delay) or a prolonged regimen (every 48 h starting at 3 days post-ICH). At 2 days post-ICH, the acute BIO treatment significantly reduced the hematoma volume. In the perihematoma regions, BIO administration blocked GSK-3β phosphorylation/activation, increased Bcl-2 and β-catenin levels, and significantly increased viability of neurons and other cell types. The prolonged BIO regimen maintained a higher level of β-catenin, upregulated VEGF and BDNF, and promoted neurogenesis and angiogenesis in peri-injury zones at 14 days after ICH. The BIO treatment also promoted proliferation of neural stem cells (NSCs) and migration of nascent DCX+ neuroblasts from the subventricular zone (SVZ) to the lesioned cortex. BIO improved functional outcomes on both the neurological severity score and rotarod tests. The findings of this study corroborate the neuroprotective and regenerative effects of BIO and suggest that the Wnt/GSK-3β/β-catenin pathway may be explored for the treatment of acute or chronic ICH.

Indexed as

AnimalsBrainCell DeathCells, CulturedCerebral HemorrhageDoublecortin ProteinFemaleGlucoseGlycogen Synthase Kinase 3IndolesIn Situ Nick-End LabelingL-Lactate DehydrogenaseMiceMice, Inbred C57BLNeurogenesisNeurons6-bromoindirubin-3'-oximeDcx protein, mouseDoublecortin ProteinGlucoseGlycogen Synthase Kinase 3IndolesL-Lactate DehydrogenaseOximesOxygen

Identifiers

PMID28195036
PMCPMC5657706
OpenAlexW2588264696

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.