Evidence map›Paper›PMID 34658794›Full record

ArticleFrontiers in cellular neuroscience2021

Neuroprotective Effects of Exogenous Irisin in Kainic Acid-Induced Status Epilepticus.

Yao Cheng, Yaru Cui, Yujie Zhai, Wenyu Xin, Yan Yu, Jia Liang, Shucui Li, Hongliu Sun

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Research progress on oxidative stress regulating different types of neuronal death caused by epileptic seizures.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Review
  12. Irisin, an Effective Treatment for Cardiovascular Diseases?Journal of cardiovascular development and disease · 2022
    Review
  13. Article
  14. Review
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.

Yao ChengSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Yaru CuiSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Yujie ZhaiSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Wenyu XinSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Yan YuSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Jia LiangSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Shucui LiSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Hongliu SunSchool of Pharmaceutical Sciences, Binzhou Medical University, Yantai, China.
Binzhou Medical University · CNBinzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elevated reactive oxygen species (ROS) level is considered a crucial causative factor for neuronal damage in epilepsy. Irisin has been reported to ameliorate mitochondrial dysfunction and to reduce ROS levels; therefore, in this study, the effect of exogenous irisin on neuronal injury was evaluated in rats with kainic acid (KA)-induced status epilepticus (SE). Our results showed that exogenous irisin treatment significantly increased the expression of brain-derived neurotrophic factor (BDNF) and uncoupling protein 2 (UCP2), and reduced the levels of neuronal injury and mitochondrial oxidative stress. Additionally, an inhibitor of UCP2 (genipin) was administered to investigate the underlying mechanism of irisin-induced neuroprotection; in rats treated with genipin, the neuroprotective effects of irisin on KA-induced SE were found to be partially reversed. Our findings confirmed the neuroprotective effects of exogenous irisin and provide evidence that these effects may be mediated via the BDNF/UCP2 pathway, thus providing valuable insights that may aid the development of exogenous irisin treatment as a potential therapeutic strategy against neuronal injury in epilepsy.

Indexed as

irisinmitochondrial oxidative stressmitophagyneuronal injurystatus epilepticus

Identifiers

PMID34658794
PMCPMC8517324
OpenAlexW3204381616

What OpenQuestion holds

Textmetadata
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.