Evidence map›Paper›PMID 26178478›Full record

ArticleInflammation2015

Anti-inflammation Effects of Oxysophoridine on Cerebral Ischemia-Reperfusion Injury in Mice.

Yong-Sheng Wang, Yu-Xiang Li, Peng Zhao, Hong-Bo Wang, Ru Zhou, Yin-Ju Hao, Jie Wang, Shu-Jing Wang, Juan Du, Lin Ma and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  12. Oncology letters · 2017
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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

12 authors at 3 institutions in 1 country.

Yong-Sheng WangDepartment of Pharmacology, Ningxia Medical University, Yinchuan, 750004, China.
Yu-Xiang LiCollege of Nursing, Ningxia Medical University, Yinchuan, 750004, China.
Peng ZhaoDepartment of Pharmacology, Ningxia Medical University, Yinchuan, 750004, China.
Hong-Bo WangDepartment of Pharmacology, Ningxia Medical University, Yinchuan, 750004, China.
Ru ZhouDepartment of Pharmacology, Ningxia Medical University, Yinchuan, 750004, China.
Yin-Ju HaoNingxia Medical University, Yinchuan, 750004, China.
Jie WangMedical Sci-Tech Research Center, Ningxia Medical University, Yinchuan, 750004, China.
Shu-Jing WangMedical Sci-Tech Research Center, Ningxia Medical University, Yinchuan, 750004, China.
Juan DuDepartment of Pharmacology, Ningxia Medical University, Yinchuan, 750004, China.
Lin MaNingxia Key Lab of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan, 750004, China.
Tao SunNingxia Key Lab of Craniocerebral Diseases of Ningxia Hui Autonomous Region, Yinchuan, 750004, China.
Jian-Qiang YuDepartment of Pharmacology, Ningxia Medical University, Yinchuan, 750004, China. yujq910315@163.com.
Ningxia Medical University · CNNingxia Seismological Bureau · CNNingxia Center for Diseases Prevention and Control · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxysophoridine (OSR) is a bioactive alkaloid extracted from the Sophora alopecuroides Linn. Our aim is to explore the potential anti-inflammation mechanism of OSR in cerebral ischemic injury. Mice were intraperitoneally pretreated with OSR (62.5, 125, and 250 mg/kg) or nimodipine (Nim) (6 mg/kg) for 7 days followed by cerebral ischemia. The inflammatory-related cytokines in cerebral ischemic hemisphere tissue were determined by immunohistochemistry staining, Western blot and enzyme-like immunosorbent assay (ELISA). OSR-treated groups observably suppressed the nuclear factor kappa B (NF-κB), intercellular adhesion molecule-1 (ICAM-1), inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2). OSR-treated group (250 mg/kg) markedly reduced the inflammatory-related protein prostaglandin E2 (PGE2), tumor necrosis factor alpha (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6), and interleukin-8 (IL-8). Meanwhile, it dramatically increased the interleukin-10 (IL-10). Our study revealed that OSR protected neurons from ischemia-induced injury in mice by downregulating the proinflammatory cytokines and blocking the NF-κB pathway.

Indexed as

AlkaloidsAnimalsAnti-Inflammatory AgentsBrainBrain IschemiaCyclooxygenase 2CytokinesDinoprostoneDisease Models, AnimalDose-Response Relationship, DrugInflammation MediatorsIntercellular Adhesion Molecule-1MaleMice, Inbred ICRNeuroprotective AgentsNitric OxideAlkaloidsAnti-Inflammatory AgentsCyclooxygenase 2CytokinesDinoprostoneIcam1 protein, mouseInflammation MediatorsIntercellular Adhesion Molecule-1Neuroprotective AgentsNitric OxideNitric Oxide Synthase Type IINos2 protein, mouseoxysophoridinePtgs2 protein, mouseRela protein, mouseTranscription Factor RelAanti-inflammationcerebral ischemiaNF-κBoxysophoridine

Identifiers

PMID26178478
OpenAlexW873768316

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.