Evidence map›Paper›PMID 37333874›Full record

ArticleTranslational neuroscience2023

Geniposide protected against cerebral ischemic injury through the anti-inflammatory effect via the NF-κB signaling pathway.

Qian Sun, Xiangjian Zhang, Jingyi Fan, Lan Zhang, Hui Ji, Jing Xue, Cong Zhang, Rong Chen, Jing Zhao, Junmin Chen and 2 more

Open access · goldAbstract read
In one paragraph

Article in Translational neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
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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 2 institutions in 1 country.

Qian SunDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Xiangjian ZhangDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Jingyi FanDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Lan ZhangDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Hui JiDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Jing XueDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Cong ZhangDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Rong ChenDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Jing ZhaoDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Junmin ChenDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Xiaoxia LiuDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Degang SongDepartment of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050000, China.
Hebei Medical University · CNSecond Hospital of Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Context: Accumulated evidence indicates that geniposide exhibits neuroprotective effects in ischemic stroke. However, the potential targets of geniposide remain unclear. Objective: We explore the potential targets of geniposide in ischemic stroke. Materials and methods: Adult male C57BL/6 mice were subjected to the middle cerebral artery occlusion (MCAO) model. Mice were randomly divided into five groups: Sham, MCAO, and geniposide-treated (i.p. twice daily for 3 days before MCAO) at doses of 25, 75, or 150 mg/kg. We first examined the neuroprotective effects of geniposide. Then, we further explored via biological information analysis and verified the underlying mechanism Results: In the current study, geniposide had no toxicity at concentrations of up to 150 mg/kg. Compared with the MCAO group, the 150 mg/kg group of geniposide significantly ( Conclusions: Geniposide exhibited a neuroprotective effect via attenuating inflammatory response, as indicated by biological information analysis,

Indexed as

A20MCAOneuroinflammationNF-KbTRAF6

Identifiers

PMID37333874
PMCPMC10276575
OpenAlexW4380089023

What OpenQuestion holds

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Registered trials

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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.