Evidence map›Paper›PMID 29642394›Full record

ArticleInternational journal of molecular sciences2018

Neuroprotective Effects of Platonin, a Therapeutic Immunomodulating Medicine, on Traumatic Brain Injury in Mice after Controlled Cortical Impact.

Ting-Lin Yen, Chao-Chien Chang, Chi-Li Chung, Wen-Chin Ko, Chih-Hao Yang, Cheng-Ying Hsieh

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. 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
2.4field-weighted citation impact, top 12% 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, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. WNT3A Promotes Neuronal Regeneration upon Traumatic Brain Injury.International journal of molecular sciences · 2020
    Article
  13. Molecular Pharmacology and Pathology of Strokes.International journal of molecular sciences · 2018
    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

6 authors at 3 institutions in 1 country.

Ting-Lin YenDepartment of Medical Research, Cathay General Hospital, Taipei 22174, Taiwan. d119096015@tmu.edu.tw.
Chao-Chien ChangDepartment of Pharmacology, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan. change@seed.net.tw.
Chi-Li ChungDivision of Pulmonary Medicine, Department of Internal Medicine, Taipei Medical University Hospital, Taipei 11031, Taiwan.. clchung@tmu.edu.tw.ORCID 0000-0003-0656-976X
Wen-Chin KoDepartment of Cardiology, Cathay General Hospital, Taipei 10630, Taiwan. wckcgh@ms17.hinet.net.
Chih-Hao YangDepartment of Pharmacology, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan. chyang@tmu.edu.tw.
Cheng-Ying HsiehDepartment of Pharmacology, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan. hsiehcy@tmu.edu.tw.
Cathay General Hospital · TWTaipei Medical University · TWTaipei Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traumatic brain injury (TBI) is one of the leading causes of mortality worldwide and leads to persistent cognitive, sensory, motor dysfunction, and emotional disorders. TBI-caused primary injury results in structural damage to brain tissues. Following the primary injury, secondary injuries which are accompanied by neuroinflammation, microglial activation, and additional cell death subsequently occur. Platonin, a cyanine photosensitizing dye, has been used to treat trauma, ulcers, and some types of acute inflammation. In the present study, the neuroprotective effects of platonin against TBI were explored in a controlled cortical impact (CCI) injury model in mice. Treatment with platonin (200 µg/kg) significantly reduced the neurological severity score, general locomotor activity, and anxiety-related behavior, and improved the rotarod performance of CCI-injured mice. In addition, platonin reduced lesion volumes, the expression of cleaved caspase-3, and microglial activation in TBI-insulted brains. Platonin also suppressed messenger (m)RNA levels of caspase-3, caspase-1, cyclooxygenase-2, tumor necrosis factor-α, interleukin-6, and interleukin-1β. On the other hand, free radical production after TBI was obviously attenuated in platonin-treated mice. Treatment with platonin exhibited prominent neuroprotective properties against TBI in a CCI mouse model through its anti-inflammatory, anti-apoptotic, and anti-free radical capabilities. This evidence collectively indicates that platonin may be a potential therapeutic medicine for use with TBIs.

Indexed as

AnimalsAnti-Inflammatory AgentsBrain Injuries, TraumaticCaspasesCerebral CortexCyclooxygenase 2Hand StrengthInterleukinsLocomotionMaleMiceMice, Inbred C57BLMicrogliaNeuroprotective AgentsThiazolesTumor Necrosis Factor-alphaAnti-Inflammatory AgentsCaspasesCyclooxygenase 2InterleukinsNeuroprotective AgentsplatoninThiazolesTumor Necrosis Factor-alphafree radicalmicroglial activationneuroinflammationplatonintraumatic brain injury

Identifiers

PMID29642394
PMCPMC5979356
OpenAlexW2796020003

What OpenQuestion 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 OpenQuestion graph.