Evidence map›Paper›PMID 32058974›Full record

ArticleiScience2020

Post-treatment with Posiphen Reduces Endoplasmic Reticulum Stress and Neurodegeneration in Stroke Brain.

Seong-Jin Yu, Kuo-Jen Wu, Eunkyung Bae, Yu-Syuan Wang, Chia-Wen Chiang, Li-Wei Kuo, Brandon K Harvey, Nigel H Greig, Yun Wang

Open access · goldAbstract read
In one paragraph

Article in iScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  6. ACS pharmacology & translational science · 2022
    Article
  7. Review
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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

9 authors at 3 institutions in 2 countries.

Seong-Jin YuCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Kuo-Jen WuCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Eunkyung BaeCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Yu-Syuan WangCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Chia-Wen ChiangInstitute of Biomedical Engineering and Nanomedicine, National Health Research Institutes, Zhunan, Miaoli, Taiwan.
Li-Wei KuoInstitute of Biomedical Engineering and Nanomedicine, National Health Research Institutes, Zhunan, Miaoli, Taiwan.
Brandon K HarveyNational Institute on Drug Abuse, NIH, Baltimore, MD, USA.
Nigel H GreigTranslational Gerontology Branch, Intramural Research Program, National Institute of Aging, NIH, Baltimore, MD, USA.
Yun WangCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan. Electronic address: ywang@nhri.edu.tw.
National Health Research Institutes · TWNational Institute on Aging · USNational Institute on Drug Abuse · US

Funding

Design And Development Of Experimental Therapeutics ((Systemic & Neurodegenerative Disorders and Alzheimer's Disease)ZIAAG000311 · NIA · NATIONAL INSTITUTE ON AGING · PI GREIG, NIGEL H. · 2009 to 2025
$16.0M
Cellular mechanisms of neuronal dysfunction in addiction and neurodegenerationZIADA000618 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI HARVEY, BRANDON · 2017 to 2025
$12.9M
6 · The paper itself

Abstract

Acetylcholinesterase (AChE) inhibitors have protective and anti-inflammatory actions against brain injury, mediated by nicotinic α7 cholinergic receptor activation. The use of AChE inhibitors in patients is limited by systemic cholinergic side effects. Posiphen, a stereoisomer of the AChE inhibitor Phenserine, lacks AChE inhibitor activity. The purpose of this study is to determine the protective effect of Posiphen in cellular and animal models of stroke. Both Posiphen and Phenserine reduced glutamate-mediated neuronal loss in co-cultures of primary cortical cells and microglia. Phenserine-, but not Posiphen-, mediated neuroprotection was diminished by the nicotinic α7 receptor antagonist methyllycaconitine. Posiphen antagonized NMDA-mediated Ca

Indexed as

Cell BiologyClinical NeuroscienceDrugsMolecular Biology

Identifiers

PMID32058974
PMCPMC7013187
OpenAlexW3002350370

What Socratic 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 Socratic graph.