Evidence map›Paper›PMID 28085110›Full record

ArticleMolecules (Basel, Switzerland)2017

Ginsenoside Rg3 Improves Recovery from Spinal Cord Injury in Rats via Suppression of Neuronal Apoptosis, Pro-Inflammatory Mediators, and Microglial Activation.

Dong-Kyu Kim, Ki-Jung Kweon, Pyungsoo Kim, Hee-Jung Kim, Sung-Soo Kim, Nak-Won Sohn, Sungho Maeng, Jung-Won Shin

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Dong-Kyu KimDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. omdkdk@empal.com.
Ki-Jung KweonDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. kgj1031@hanmail.net.
Pyungsoo KimDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. bixas@hanmail.net.
Hee-Jung KimDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. noonkkot@hanmail.net.
Sung-Soo KimDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. kokoajam@gmail.com.
Nak-Won SohnDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. sohnnw@khu.ac.kr.
Sungho MaengDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. jethrot@khu.ac.kr.
Jung-Won ShinDepartment of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 17404, Korea. shinarago@khu.ac.kr.
Kyung Hee University East-West Neo Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal cord injury (SCI) is one of the most devastating medical conditions; however, currently, there are no effective pharmacological interventions for SCI. Ginsenoside Rg3 (GRg3) is one of the protopanaxadiols that show anti-inflammatory, anti-oxidant, and neuroprotective effects. The present study investigated the neuroprotective effect of GRg3 following SCI in rats. SCI was induced using a static compression model at vertebral thoracic level 10 for 5 min. GRg3 was administrated orally at a dose of 10 or 30 mg/kg/day for 14 days after the SCI. GRg3 (30 mg/kg) treatment markedly improved behavioral motor functions, restored lesion size, preserved motor neurons in the spinal tissue, reduced Bax expression and number of TUNEL-positive cells, and suppressed mRNA expression of pro-inflammatory cytokines including tumor necrosis factor-α, interleukin (IL)-1β, and IL-6. GRg3 also attenuated the over-production of cyclooxygenase-2 and inducible nitric oxide synthase after SCI. Moreover, GRg3 markedly suppressed microglial activation in the spinal tissue. In conclusion, GRg3 treatment led to a remarkable recovery of motor function and a reduction in spinal tissue damage by suppressing neuronal apoptosis and inflammatory responses after SCI. These results suggest that GRg3 may be a potential therapeutic agent for the treatment of SCI.

Indexed as

AnimalsAnti-Inflammatory AgentsApoptosisGene Expression RegulationGinsenosidesHumansInflammation MediatorsMicrogliaNeuronsNeuroprotective AgentsOxidative StressRatsRats, Sprague-DawleySapogeninsSpinal CordSpinal Cord InjuriesAnti-Inflammatory Agentsginsenoside Rg3GinsenosidesInflammation MediatorsNeuroprotective AgentsprotopanaxatriolSapogeninsapoptosisginsenoside Rg3microglial activationmotor functionpro-inflammatory cytokinesspinal cord injury

Identifiers

PMID28085110
PMCPMC6155773
OpenAlexW2579028310

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.