Evidence map›Paper›PMID 26113792›Full record

ArticleExperimental neurobiology2015

Growth Differentiation Factor 15 Expression in Astrocytes After Excitotoxic Lesion in the Mouse Hippocampus.

Min-Hee Yi, Enji Zhang, Hyunjung Baek, Sena Kim, Nara Shin, Joon Won Kang, Sunyeul Lee, Sang-Ha Oh, Dong Woon Kim

Open access · bronzeAbstract read
In one paragraph

Article in Experimental neurobiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. GDF15, an update of the physiological and pathological roles it plays: a review.Pflugers Archiv : European journal of physiology · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

9 authors at 2 institutions in 1 country.

Min-Hee YiDepartment of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea.
Enji ZhangDepartment of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea.
Hyunjung BaekDepartment of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea. ; Department of Pediatrics, Chungnam National University Hospital, Daejeon 301-721, Korea.
Sena KimDepartment of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea. ; Department of Plastic Surgery, Chungnam National University Hospital, Daejeon 301-721, Korea.
Nara ShinDepartment of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea. ; Department of Anesthesia and Pain Medicine, Chungnam National University Hospital, Daejeon 301-721, Korea.
Joon Won KangDepartment of Pediatrics, Chungnam National University Hospital, Daejeon 301-721, Korea.
Sunyeul LeeDepartment of Anesthesia and Pain Medicine, Chungnam National University Hospital, Daejeon 301-721, Korea.
Sang-Ha OhDepartment of Plastic Surgery, Chungnam National University Hospital, Daejeon 301-721, Korea.
Dong Woon KimDepartment of Anatomy, Brain Research Institute, Chungnam National University School of Medicine, Daejeon 301-747, Korea.
Chungnam National University · KRChungnam National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growth differentiation factor 15 (GDF15) is, a member of the transforming growth factor β (TGF-β) superfamily of proteins. Although GDF15 is well established as a potent neurotrophic factor for neurons, little is known about its role in glial cells under neuropathological conditions. We monitored GDF15 expression in astrocyte activation after a kainic acid (KA)-induced neurodegeneration in the ICR mice hippocampus. In control, GDF15 immunoreactivity (IR) was evident in the neuronal layer of the hippocampus; however, GDF15 expression had increased in activated astrocytes throughout the hippocampal region at day 3 after the treatment with KA. LPS treatment in astrocytes dramatically increased GDF15 expression in primary astrocytes. In addition, LPS treatment resulted in the decrease of the IκB-α degradation and increase of the phosphorylation level of RelA/p65. These results indicate that GDF15 has a potential link to NF-κB activation, making GDF15 a valuable target for modulating inflammatory conditions.

Indexed as

AstrocyteExcitotoxicityGDF15NF kappaB signaling

Identifiers

PMID26113792
PMCPMC4479809
OpenAlexW2157904425

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.