Evidence map›Paper›PMID 33402180›Full record

ArticleBMC complementary medicine and therapies2021

Germacrone alleviates neurological deficits following traumatic brain injury by modulating neuroinflammation and oxidative stress.

Sujing Zhuang, Baogui Liu, Shifeng Guo, Yanzhong Xue, Lin Wu, Shiqi Liu, Chunling Zhang, Xiuyan Ni

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  3. Antioxidant Potential and Oxidative Stress Modulation ofPharmaceuticals (Basel, Switzerland) · 2025
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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 2 institutions in 1 country.

Sujing ZhuangDepartment of Neurology, Linyi Central Hospital, Linyi, 276400, Shandong, China.
Baogui LiuDepartment of Anesthesiology, Linyi Central Hospital, Linyi, 276400, Shandong, China.
Shifeng GuoDepartment of Neurology, Linyi Central Hospital, Linyi, 276400, Shandong, China.
Yanzhong XueDepartment of Neurology, Linyi Central Hospital, Linyi, 276400, Shandong, China.
Lin WuDepartment of Intensive Care Unit 2, Affiliated Hospital of Jining Medical University, Jining, 272000, Shandong, China.
Shiqi LiuDepartment of Gastrointestinal Surgery, Affiliated Hospital of Jining Medical University, Jining, 272000, Shandong, China.
Chunling ZhangDepartment of Intensive Care Unit 2, Affiliated Hospital of Jining Medical University, Jining, 272000, Shandong, China.
Xiuyan NiDepartment of Radiotherapy, Linyi Central Hospital, Linyi, 276400, Shandong, China. mgpjfnuxiemu8211@163.com.ORCID http://orcid.org/0000-0002-7320-6937
Linyi People's Hospital · CNAffiliated Hospital of Jining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGermacrone (GM) is a terpenoid compound which is reported to have anti-inflammatory and anti-oxidative effects. However, its role in treating traumatic brain injury (TBI) remains largely unknown.

methodsMale C57BL/6 mice were divided into the following groups: control group, TBI group [controlled cortical impact (CCI) model], CCI + 5 mg/kg GM group, CCI + 10 mg/kg GM group and CCI + 20 mg/kg GM group. GM was administered via intraperitoneal injection. The neurological functions (including motor coordination, spatial learning and memory abilities) and brain edema were measured. Nissl staining was used to detect the neuronal apoptosis. Colorimetric assays and enzyme linked immunosorbent assay (ELISA) kits were used to determine the expression levels of oxidative stress markers including myeloperoxidase (MPO), malondialdehyde (MDA) and superoxide dismutase (SOD), as well as the expressions of inflammatory markers, including tumor necrosis factor α (TNF-α), interleukin-1β (IL-1β) and interleukin-6 (IL-6). Additionally, protein levels of Nrf2 and p-p65 were detected by Western blot assay.

resultsGM significantly ameliorated motor dysfunction, spatial learning and memory deficits of the mice induced by TBI and it also reduced neuronal apoptosis and microglial activation in a dose-dependent manner. Besides, GM treatment reduced neuroinflammation and oxidative stress compared to those in the CCI group in a dose-dependent manner. Furthermore, GM up-regulated the expression of antioxidant protein Nrf2 and inhibited the expression of inflammatory response protein p-p65.

conclusionsGM is a promising drug to improve the functional recovery after TBI via repressing neuroinflammation and oxidative stress.

Indexed as

AnimalsBrainBrain EdemaBrain Injuries, TraumaticCurcumaCytokinesDisease Models, AnimalDrug Evaluation, PreclinicalMaleMemoryMiceMice, Inbred C57BLMicrogliaNervous System DiseasesNF-E2-Related Factor 2NF-kappa BCytokinesgermacroneNfe2l2 protein, mouseNF-E2-Related Factor 2NF-kappa BPlant ExtractsSesquiterpenes, GermacraneGermacroneInflammationNF-κBTraumatic brain injury

Identifiers

PMID33402180
PMCPMC7786997
OpenAlexW3118280692

What OpenQuestion holds

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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.