Evidence map›Paper›PMID 24985053›Full record

ArticleScientific reports2014

Nafamostat mesilate attenuates neuronal damage in a rat model of transient focal cerebral ischemia through thrombin inhibition.

Tao Chen, Jing Wang, Chenhui Li, Weining Zhang, Luyong Zhang, Lufan An, Tao Pang, Xinzhong Shi, Hong Liao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.3field-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

23 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Acute kidney injury in neurocritical care.Critical care (London, England) · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  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

9 authors at 1 institution in 1 country.

Tao ChenJiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, P.R.China.
Jing WangJiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, P.R.China.
Chenhui LiJiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, P.R.China.
Weining ZhangSchool of Medical Science and Laboratory Medicine, Jiangsu University, Zhenjiang 212013, P.R.China.
Luyong ZhangJiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, P.R.China.
Lufan AnJiangsu D&R Pharmaceutical Co. LTD, Taizhou 225300, P.R.China.
Tao PangJiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, P.R.China.
Xinzhong ShiSchool of Science, China Pharmaceutical University, Nanjing 210009, P.R.China.
Hong LiaoJiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, P.R.China.
China Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence suggests that thrombin, a blood coagulation serine protease, mediates neuronal injury in experimental cerebral ischemia. Here, we test the hypothesis that nafamostat mesilate, a serine protease inhibitor, may ameliorate ischemia-induced neuronal damage through thrombin inhibition after ischemic stroke. Focal ischemia was induced in adult Sprague-Dawley rats by occlusion of the middle cerebral artery for 2 hours followed by 22 hours of reperfusion. The administration of nafamostat mesilate during ischemia and reperfusion reduced the brain infarct volume, edema volume and neurological deficit. Thrombin expression and activity in the ipsilateral striatum were increased after ischemia, whereas the administration of nafamostat mesilate significantly inhibited thrombin expression and activity. Immunostaining showed that the majority of thrombin was expressed in neurons. TUNEL staining showed that nafamostat mesilate reduced the number of dying cells during ischemia. A rat behavioral test showed that nafamostat mesilate treatment significantly improved the learning ability of ischemic rats. These results suggest that nafamostat mesilate may have a potential therapeutic role for neuroprotection against focal cerebral ischemia through thrombin inhibition.

Indexed as

AnimalsAntithrombinsBenzamidinesBrain IschemiaDose-Response Relationship, DrugFibrinolysinGuanidinesMaleNeuronsNeuroprotective AgentsRatsRats, Sprague-DawleyThrombinTreatment OutcomeAntithrombinsBenzamidinesFibrinolysinGuanidinesnafamostatNeuroprotective AgentsThrombin

Identifiers

PMID24985053
PMCPMC4078306
OpenAlexW1977186831

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.