Evidence map›Paper›PMID 36134852›Full record

ArticleActa cirurgica brasileira2022

The neuroprotective effects of Lutongkeli in traumatic brain injury rats by anti-apoptosis mechanism.

Qiu-Xia Xiao, Lu-Lu Xue, Zhang-Yu Su, Jin Huang, Ji-Lin Chen, Liu-Lin Xiong, Ting-Hua Wang

Open access · goldAbstract read
In one paragraph

Article in Acta cirurgica brasileira, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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 3 institutions in 1 country.

Qiu-Xia XiaoMD. Kunming Medical University - Institute of Neuroscience - Animal Zoology Department - Kunming, China.ORCID http://orcid.org/0000-0002-7552-4947
Lu-Lu XuePhD. Sichuan University - State Key Laboratory of Biotherapy - Chengdu, China.ORCID http://orcid.org/0000-0001-5253-7158
Zhang-Yu SuBS. Southwest Medical University - Department of Anesthesiology - Luzhou, China.ORCID http://orcid.org/0000-0002-7459-9402
Jin HuangPhD. Kunming Medical University - Affiliated Hospital - Department of Neurosurgery - Kunming, China.ORCID http://orcid.org/0000-0003-2285-2274
Ji-Lin ChenBS. Kunming Medical University - Institute of Neuroscience - Animal Zoology Department - Kunming, China.ORCID http://orcid.org/0000-0002-8031-9278
Liu-Lin XiongPhD, Professor. Kunming Medical University - Institute of Neuroscience - Animal Zoology Department - Kunming, China.ORCID http://orcid.org/0000-0002-1623-5969
Ting-Hua WangPhD, Professor. Kunming Medical University - Institute of Neuroscience - Animal Zoology Department - Kunming, China.ORCID http://orcid.org/0000-0003-2012-8936
Kunming Medical University · CNSichuan University · CNSouthwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo explore the neuroprotective effects of Lutongkeli (LTKL) in traumatic brain injury (TBI) and detect the related mechanism.

methodsTBI model was established with LTKL administration (2 and 4 g/kg/d, p.o.). Motor function of rats was examined by Rotarod test. Nissl staining was used to show neuron morphology. Furthermore, the disease-medicine common targets were obtained with the network pharmacology and analyzed with Kyoto Encyclopedia of Genes and Genomes. Lastly, the predicted targets were validated by real-time polymerase chain reaction.

resultsAfter LTKL administration, neural behavior was significantly improved, and the number of spared neurons in brain was largely increased. Moreover, 68 bioactive compounds were identified, corresponding to 148 LTKL targets; 2,855 genes were closely associated with TBI, of which 87 overlapped with the LTKL targets and were considered to be therapeutically relevant. Functional enrichment analysis suggested LTKL exerted its pharmacological effects in TBI by modulating multiple pathways including apoptosis, inflammation, etc. Lastly, we found LTKL administration could increase the mRNA level of Bcl-2 and decrease the expression of Bax and caspase-3.

conclusionsThis study reported the neuroprotective effect of LTKL against TBI is accompanied with anti-apoptosis mechanism, which provides a scientific explanation for the clinical application of LTKL in the treatment of TBI.

Indexed as

Brain Injuries, TraumaticNeuroprotective AgentsAnimalsbcl-2-Associated X ProteinCaspase 3Disease Models, AnimalProto-Oncogene Proteins c-bcl-2RatsRats, Sprague-DawleyRNA, Messengerbcl-2-Associated X ProteinCaspase 3Neuroprotective AgentsProto-Oncogene Proteins c-bcl-2RNA, Messenger

Identifiers

PMID36134852
PMCPMC9488509
OpenAlexW4296375268

What OpenQuestion holds

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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.