Evidence map›Paper›PMID 27452038›Full record

ArticleNeurochemical research2016

Tetramethylpyrazine Nitrone Improves Neurobehavioral Functions and Confers Neuroprotection on Rats with Traumatic Brain Injury.

Gaoxiao Zhang, Fen Zhang, Tao Zhang, Jianbo Gu, Cuimei Li, Yewei Sun, Pei Yu, Zaijun Zhang, Yuqiang Wang

Abstract read
PubMed Publisher
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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Induction of Heme Oxygenase-1 by 15d-Prostaglandin JAntioxidants (Basel, Switzerland) · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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.

Gaoxiao ZhangInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Fen ZhangInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Tao ZhangInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Jianbo GuInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Cuimei LiInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Yewei SunInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Pei YuInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Zaijun ZhangInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China. zaijunzhang@163.com.ORCID http://orcid.org/0000-0002-0690-1673
Yuqiang WangInstitute of New Drug Research, Jinan University College of Pharmacy, Huangpu Road, Guangzhou, 510632, China.
Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress is one of the major secondary injury mechanisms after traumatic brain injury (TBI). 2-[[(1,1-Dimethylethyl)oxidoimino]-methyl]-3,5,6-trimethylpyrazine (TBN), a derivative of the clinically used anti-stroke drug tetramethylpyrazine armed with a powerful free radical-scavenging nitrone moiety, has been demonstrated promising therapeutic efficacy in ischemic stroke and Parkinson's models. The present study aims to investigate the effects of TBN on behavioral function and neuroprotection in rats subjected to TBI. TBN (90 mg/kg) was administered twice daily for 7 days by intravenous injection following TBI. TBN improved neuronal behavior functions after brain injury, including rotarod test and adhesive paper removal test. Compared with the TBI model group, TBN treatment significantly protected NeuN-positive neurons, while decreased glial fibrillary acidic protein (GFAP)-positive cells. The number of 4-hydroxynonenal (4-HNE)-positive and 8-hydroxy-2'-deoxyguanosine (8-OHdG)-positive cells around the damaged area after TBI were significantly decreased in the TBN treatment group. In addition, TBN effectively reversed the altered expression of Bcl-2, Bax and caspase 3, and the down-regulation of nuclear factor erythroid-derived 2-like 2 (Nrf-2) and hemeoxygenase-1 (HO-1) proteins expression stimulated by TBI. In conclusion, TBN improves neurobehavioral functions and protects neurons against TBI. This protective effect may be achieved by anti-neuronal apoptosis, alleviating oxidative stress damage and up-regulating Nrf-2 and HO-1 expression.

Indexed as

AnimalsApoptosisBrain Injuries, TraumaticCaspase 3Down-RegulationFree Radical ScavengersMaleNeuronsNeuroprotectionNeuroprotective AgentsNitrogen OxidesOxidative StressPyrazinesRats, Sprague-DawleyCasp3 protein, ratCaspase 3Free Radical ScavengersNeuroprotective AgentsNitrogen OxidesnitronesPyrazinestetramethylpyrazineApoptosisHO-1NeuroprotectionNrf-2Oxidative stress

Identifiers

PMID27452038
OpenAlexW2478252298

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.