Evidence map›Paper›PMID 27161367›Full record

ArticleNeurochemical research2016

Treatment with Isorhamnetin Protects the Brain Against Ischemic Injury in Mice.

Jin-Jing Zhao, Jin-Qing Song, Shu-Yi Pan, Kai Wang

Abstract read
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In one paragraph

Article in Neurochemical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Investigation of Anticonvulsant Potential ofInternational journal of molecular sciences · 2025
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  8. Article
  9. Neurotrophic Natural Products.Progress in the chemistry of organic natural products · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Isorhamnetin Attenuated the Release of Interleukin-6 fromOxidative medicine and cellular longevity · 2022
    Article
  17. Review
  18. Article
  19. Article
  20. 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

4 authors at 3 institutions in 1 country.

Jin-Jing ZhaoDepartment of Neurology, 305th Hospital of the People's Liberation Army, Jia13 Wenjin Road, Beijing, 100017, China.
Jin-Qing SongDepartment of Pediatrics, Peking University First Hospital, Beijing, 100034, China.
Shu-Yi PanDepartment of Hyperbaric Oxygen, Navy General Hospital of People's Liberation Army, Beijing, 100048, China.
Kai WangDepartment of Neurology, 305th Hospital of the People's Liberation Army, Jia13 Wenjin Road, Beijing, 100017, China. wangkwangk92@163.com.
305 Hospital of People Liberation Army · CNPeking University · CNPLA Navy General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic stroke is a major cause of morbidity and mortality, yet lacks effective neuroprotective treatments. The aim of this work was to investigate whether treatment with isorhamnetin protected the brain against ischemic injury in mice. Experimental stroke mice underwent the filament model of middle cerebral artery occlusion with reperfusion. Treatment with isorhamnetin or vehicle was initiated immediately at the onset of reperfusion. It was found that treatment of experimental stroke mice with isorhamnetin reduced infarct volume and caspase-3 activity (a biomarker of apoptosis), and improved neurological function recovery. Treatment of experimental stroke mice with isorhamnetin attenuated cerebral edema, improved blood-brain barrier function, and upregulated gene expression of tight junction proteins including occludin, ZO-1, and claudin-5. Treatment of experimental stroke mice with isorhamnetin activated Nrf2/HO-1, suppressed iNOS/NO, and led to reduced formation of MDA and 3-NT in ipsilateral cortex. In addition, treatment of experimental stroke mice with isorhamnetin suppressed activity of MPO (a biomarker of neutrophil infiltration) and reduced protein levels of IL-1β, IL-6, and TNF-α in ipsilateral cortex. Furthermore, it was found that treatment of experimental stroke mice with isorhamnetin reduced mRNA and protein expression of NMDA receptor subunit NR1 in ipsilateral cortex. In conclusion, treatment with isorhamnetin protected the brain against ischemic injury in mice. Isorhamnetin could thus be envisaged as a countermeasure for ischemic stroke but remains to be tested in humans.

Indexed as

AnimalsBrainBrain IschemiaMaleMiceMice, Inbred ICRNeuroprotective AgentsOxidative StressQuercetinTreatment Outcome3-methylquercetinNeuroprotective AgentsQuercetinEdemaInflammationIschemic strokeIsorhamnetinOxidative stress

Identifiers

PMID27161367
OpenAlexW2346913409

What OpenQuestion holds

Textmetadata
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.