Evidence map›Paper›PMID 24284395›Full record

ArticleInternational journal of molecular sciences2013

Combination BMSC and Niaspan treatment of stroke enhances white matter remodeling and synaptic protein expression in diabetic rats.

Xinchun Ye, Tao Yan, Michael Chopp, Alex Zacharek, Ruizhuo Ning, Poornima Venkat, Cynthia Roberts, Jieli Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Cell-Based and Exosome Therapy in Diabetic Stroke.Stem cells translational medicine · 2018
    Article
  6. Article
  7. White matter injury in ischemic stroke.Progress in neurobiology · 2016
    Review
  8. Therapy Effects of Bone Marrow Stromal Cells on Ischemic Stroke.Oxidative medicine and cellular longevity · 2016
    Review
  9. Review
  10. Article
  11. 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 3 institutions in 2 countries.

Xinchun YeDepartment of Neurology, the Affiliated Hospital of Xuzhou Medical College, Xuzhou 221002, China. jieli@neuro.hfh.edu.
Tao Yan
Michael Chopp
Alex Zacharek
Ruizhuo Ning
Poornima Venkat
Cynthia Roberts
Jieli Chen
Henry Ford Hospital · USTianjin Medical University General Hospital · CNXuzhou Medical College · CN

Funding

Neurorestorative therapy of stroke with agents that increase HDLR01AG031811 · NIA · HENRY FORD HEALTH SYSTEM · PI CHEN, JIELI · 2009 to 2013
$1.4M
Neuroprotective therapy of stroke with HUCNC and simvastatinR41NS064708 · NINDS · SANERON CCEL THERAPEUTICS, INC. · PI CHEN, JIELI · 2010 to 2010
$177k
NIA NIH HHS R01 AG031811NINDS NIH HHS 1R41NS064708NINDS NIH HHS R41 NS064708
6 · The paper itself

Abstract

objectiveWhite matter remodeling plays an important role in neurological recovery after stroke. Bone marrow stromal cells (BMSCs) and Niaspan, an agent which increases high density lipoprotein (HDL), each induces neurorestorative effects and promotes white matter remodeling after stroke in non-diabetic rats. In this study, we test whether combination of BMSCs with Niaspan induces an enhanced white matter remodeling in the ischemic brain of diabetic rats. RESEARCH DESIGN AND

methodsType-1 diabetes (T1DM) rats were subjected to transient middle cerebral artery occlusion (MCAo) and treated with or without BMSCs; Niaspan; and the combination of BMSCs + Niaspan daily for 14 days after MCAo. Immunostaining for white matter remodeling and synaptic protein expression including NG2; CNPase; BS (Bielschowsky silver); LFB (luxol fast blue); Synaptophysin and SMI-31 immunostaining were performed.

resultsBMSC monotherapy did not regulate NG2 and CNPase expression compared to T1DM control rats. Both, combination of BMSCs + Niaspan treatment, and Niaspan monotherapy significantly increase NG2 and CNPase expression compared to T1DM control. While combination BMSC+Niaspan, BMSC monotherapy and Niaspan monotherapy groups all increase BS, LFB, synaptophysin, and SMI-31 expression in the ischemic brain compared to T1DM-MCAo control. In addition, the combination treatment significantly enhances LFB, SMI-31, and Synaptophysin expression compared to BMSC monotherapy.

conclusionsCombination treatment of stroke with BMSCs and Niaspan in T1DM rats increases white matter remodeling and additively increases BMSC monotherapy induced myelination and synaptic plasticity after stroke in T1DM rats.

Indexed as

Mesenchymal Stem CellsProtein BiosynthesisAnimalsBrainDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Lipoproteins, HDLNiacinRatsStrokeSynapsesLipoproteins, HDLNiacin

Identifiers

PMID24284395
PMCPMC3856061
OpenAlexW2164172409

What OpenQuestion holds

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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.