Evidence map›Paper›PMID 35951202›Full record

ArticleNeurochemical research2022

MiR-182 Inhibition Protects Against Experimental Stroke in vivo and Mitigates Astrocyte Injury and Inflammation in vitro via Modulation of Cortactin Activity.

Qasim M Alhadidi, Lijun Xu, Xiaoyun Sun, Yusuf S Althobaiti, Atiah Almalki, Hashem O Alsaab, Creed M Stary

Open access · greenAbstract read
In one paragraph

Article in Neurochemical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.2field-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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Perspective and Therapeutic Potential of the Noncoding RNA-Connexin Axis.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Role of miR-182 in cardiovascular and cerebrovascular diseases.Frontiers in cell and developmental biology · 2023
    Review
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 4 institutions in 3 countries.

Qasim M AlhadidiDepartment of Anesthesiology, Perioperative and Pain Medicine, School of Medicine, Stanford University, 300 Pasteur Drive, Stanford, CA, 94305-5117, USA.
Lijun XuDepartment of Anesthesiology, Perioperative and Pain Medicine, School of Medicine, Stanford University, 300 Pasteur Drive, Stanford, CA, 94305-5117, USA.
Xiaoyun SunDepartment of Anesthesiology, Perioperative and Pain Medicine, School of Medicine, Stanford University, 300 Pasteur Drive, Stanford, CA, 94305-5117, USA.
Yusuf S AlthobaitiDepartment of Pharmacology and Toxicology, College of Pharmacy, Taif University, Taif, Saudi Arabia.
Atiah AlmalkiAddiction and Neuroscience Research Unit, College of Pharmacy, Taif University, Taif, Saudi Arabia.
Hashem O AlsaabAddiction and Neuroscience Research Unit, College of Pharmacy, Taif University, Taif, Saudi Arabia.
Creed M StaryDepartment of Anesthesiology, Perioperative and Pain Medicine, School of Medicine, Stanford University, 300 Pasteur Drive, Stanford, CA, 94305-5117, USA. cstary@stanford.edu.ORCID http://orcid.org/0000-0001-9876-6634
Taif University · SAStanford University · USAl Yarmouk University College · IQStanford Medicine · US

Funding

Non-coding RNA regulation of sex differences in strokeR01NS107445 · NINDS · STANFORD UNIVERSITY · PI STARY, CREED MICHAEL · 2019 to 2023
$1.8M
American Heart Association 14FTF19970029NIH HHS NS119462NINDS NIH HHS R01 NS107445
6 · The paper itself

Abstract

Ischemic stroke remains a devastating cerebrovascular disease that accounts for a high proportion of mortality and disability worldwide. MicroRNAs (miRNAs) are a class of small non-coding RNAs that are responsible for regulation of post-transcriptional gene expression, and growing evidence supports a role for miRNAs in stroke injury and recovery. The current study examined the role of miR-182 in experimental stroke using both in vitro and in vivo models of ischemic injury. Brain levels of miR-182 significantly increased after transient middle cerebral artery occlusion (MCAO) in mice and in primary astrocyte cultures subjected to combined oxygen-glucose deprivation/reperfusion (OGD/R) injury. In vivo, stroke volume and neurological score were significantly improved by pre-treatment with miR-182 antagomir. Astrocyte cultures stressed with OGD/R resulted in mitochondrial fragmentation and downregulation of cortactin, an actin-binding protein. Inhibition of miR-182 significantly preserved cortactin expression, reduced mitochondrial fragmentation and improved astrocyte survival after OGD/R. In parallel, lipopolysaccharide (LPS)-induced nitric-oxide release in astrocyte cultures was significantly reduced by miR-182 inhibition, translating to reduced injury in primary neuronal cultures subjected to conditioned medium from LPS-treated astrocytes. These findings identify miR-182 and/or cortactin as potential clinical targets to preserve mitochondrial structure and mitigate neuroinflammation and cell death after ischemic stroke.

Indexed as

Brain IschemiaMicroRNAsReperfusion InjuryStrokeAnimalsApoptosisAstrocytesCortactinGlucoseInflammationIschemic StrokeLipopolysaccharidesMiceOxygenCortactinGlucoseLipopolysaccharidesMicroRNAsMirn182 microRNA, mouseOxygenCerebral ischemiaCytoskeletonGliamicroRNAMitochondriaOxidative stress

Identifiers

PMID35951202
PMCPMC10069410
OpenAlexW4290805576

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.