Evidence map›Paper›PMID 27164087›Full record

ArticleInternational journal of molecular sciences2016

Mechanism of Mitochondrial Connexin43's Protection of the Neurovascular Unit under Acute Cerebral Ischemia-Reperfusion Injury.

Shuai Hou, Ping-Ping Shen, Ming-Ming Zhao, Xiu-Ping Liu, Hong-Yan Xie, Fang Deng, Jia-Chun Feng

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Role of astrocytes connexins - pannexins in acute brain injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. GJA1-20k and Mitochondrial Dynamics.Frontiers in physiology · 2022
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

7 authors at 1 institution in 1 country.

Shuai HouDepartment of Neurology and Neuroscience center, the First Hospital of Jilin University, Changchun 130021, China. houshuai0310@163.com.
Ping-Ping ShenDepartment of Neurology and Neuroscience center, the First Hospital of Jilin University, Changchun 130021, China. blush135@163.com.
Ming-Ming ZhaoDepartment of Neurology and Neuroscience center, the First Hospital of Jilin University, Changchun 130021, China. zhaommchn@163.com.
Xiu-Ping LiuDepartment of Neurology and Neuroscience center, the First Hospital of Jilin University, Changchun 130021, China. liuxiuping12345@163.com.
Hong-Yan XieDepartment of Neurology and Neuroscience center, the First Hospital of Jilin University, Changchun 130021, China. xiehy321@163.com.
Fang DengDepartment of Neurology and Neuroscience center, the First Hospital of Jilin University, Changchun 130021, China. dengfang1212@126.com.
Jia-Chun FengDepartment of Neurology and Neuroscience center, the First Hospital of Jilin University, Changchun 130021, China. fengjcfrank@126.com.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We observed mitochondrial connexin43 (mtCx43) expression under cerebral ischemia-reperfusion (I/R) injury, analyzed its regulation, and explored its protective mechanisms. Wistar rats were divided into groups based on injections received before middle cerebral artery occlusion (MCAO). Cerebral infarction volume was detected by 2,3,5-triphenyltetrazolim chloride staining, and cell apoptosis was observed by transferase dUTP nick end labeling. We used transmission electron microscopy to observe mitochondrial morphology and determined superoxide dismutase (SOD) activity and malondialdehyde (MDA) content. MtCx43, p-mtCx43, protein kinase C (PKC), and p-PKC expression were detected by Western blot. Compared with those in the IR group, cerebral infarction volumes in the carbenoxolone (CBX) and diazoxide (DZX) groups were obviously smaller, and the apoptosis indices were down-regulated. Mitochondrial morphology was damaged after I/R, especially in the IR and 5-hydroxydecanoic acid (5-HD) groups. Similarly, decreased SOD activity and increased MDA were observed after MCAO; CBX, DZX, and phorbol-12-myristate-13-acetate (PMA) reduced mitochondrial functional injury. Expression of mtCx43 and p-mtCx43 and the p-Cx43/Cx43 ratio were significantly lower in the IR group than in the sham group. These abnormalities were ameliorated by CBX, DZX, and PMA. MtCx43 may protect the neurovascular unit from acute cerebral IR injury via PKC activation induced by mitoKATP channel agonists.

Indexed as

AnimalsApoptosisCerebral CortexConnexin 43Infarction, Middle Cerebral ArteryMaleMalondialdehydeMitochondriaMitochondrial ProteinsProtein Kinase CRatsRats, WistarSuperoxide DismutaseConnexin 43MalondialdehydeMitochondrial ProteinsProtein Kinase CSuperoxide Dismutasecerebral ischemia-reperfusionmitochondriamitochondrial ATP-sensitive K+ channelmitochondrial connexin43protein kinase C

Identifiers

PMID27164087
PMCPMC4881505
OpenAlexW2345976856

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.