Evidence map›Paper›PMID 24172582›Full record

ArticleStroke2013

Bryostatin improves survival and reduces ischemic brain injury in aged rats after acute ischemic stroke.

Zhenjun Tan, Ryan C Turner, Rachel L Leon, Xinlan Li, Jarin Hongpaisan, Wen Zheng, Aric F Logsdon, Zachary J Naser, Daniel L Alkon, Charles L Rosen and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Stroke, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.3field-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

38 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
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  4. Marine-derived Compounds: A Powerful Platform for the Treatment of Alzheimer's Disease.Central nervous system agents in medicinal chemistry · 2024
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  9. Putative role of natural products as Protein Kinase C modulator in different disease conditions.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2021
    Review
  10. Article
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  12. Prodrugs of PKC modulators show enhanced HIV latency reversal and an expanded therapeutic window.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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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

11 authors at 1 institution in 1 country.

Zhenjun TanFrom the Department of Neurosurgery, School of Medicine (Z.T., R.C.T., R.L.L., X.L., Z.J.N., C.L.R.), Blanchette Rockefeller Neuroscience Institute (J.H., W.Z., D.L.A.), and Department of Basic Pharmaceutical Science, School of Pharmacy (A.F.L., J.D.H.), West Virginia University Health Sciences Center, Morgantown, WV.
Ryan C Turner
Rachel L Leon
Xinlan Li
Jarin Hongpaisan
Wen Zheng
Aric F Logsdon
Zachary J Naser
Daniel L Alkon
Charles L Rosen
Jason D Huber
Blanchette Rockefeller Neurosciences Institute · US

Funding

Age influences neuropoietic signaling at the neurovascular unit following strokeR01NS061954 · NINDS · WEST VIRGINIA UNIVERSITY · PI HUBER, JASON D · 2008 to 2012
$1.7M
NINDS NIH HHS R01 NS061954
6 · The paper itself

Abstract

background and purposeBryostatin, a potent protein kinase C (PKC) activator, has demonstrated therapeutic efficacy in preclinical models of associative memory, Alzheimer disease, global ischemia, and traumatic brain injury. In this study, we tested the hypothesis that administration of bryostatin provides a therapeutic benefit in reducing brain injury and improving stroke outcome using a clinically relevant model of cerebral ischemia with tissue plasminogen activator reperfusion in aged rats.

methodsAcute cerebral ischemia was produced by reversible occlusion of the right middle cerebral artery (MCAO) in 18- to 20-month-old female Sprague-Dawley rats using an autologous blood clot with tissue plasminogen activator-mediated reperfusion. Bryostatin was administered at 6 hours post-MCAO, then at 3, 6, 9, 12, 15, and 18 days after MCAO. Functional assessment was conducted at 2, 7, 14, and 21 days after MCAO. Lesion volume and hemispheric swelling/atrophy were performed at 2, 7, and 21 days post-MCAO. Histological assessment of PKC isozymes was performed at 24 hours post-MCAO.

resultsBryostatin-treated rats showed improved survival post-MCAO, especially during the first 4 days. Repeated administration of bryostatin post-MCAO resulted in reduced infarct volume, hemispheric swelling/atrophy, and improved neurological function at 21 days post-MCAO. Changes in αPKC expression and εPKC expression in neurons were noted in bryostatin-treated rats at 24 hours post-MCAO.

conclusionsRepeated bryostatin administration post-MCAO protected the brain from severe neurological injury post-MCAO. Bryostatin treatment improved survival rate, reduced lesion volume, salvaged tissue in infarcted hemisphere by reducing necrosis and peri-infarct astrogliosis, and improved functional outcome after MCAO.

Indexed as

AnimalsApoptosisAstrocytesBrainBrain IschemiaBryostatinsDisease Models, AnimalFemaleGliosisNeuronsProtein Kinase CProtein Kinase InhibitorsRatsRats, Sprague-DawleyStrokeSurvival RateBryostatinsProtein Kinase CProtein Kinase Inhibitorsagingblood-brain barrierinfarctionprotein kinase Ctissue plasminogen activator

Identifiers

PMID24172582
PMCPMC4041549
OpenAlexW2147150250

What OpenQuestion holds

Textmetadata
LicenceTDM
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.