Evidence map›Paper›PMID 34389795›Full record

ArticleScientific reports2021

Mitochondrial dysfunction associated with autophagy and mitophagy in cerebrospinal fluid cells of patients with delayed cerebral ischemia following subarachnoid hemorrhage.

Dong Hyuk Youn, Youngmi Kim, Bong Jun Kim, Myeong Seon Jeong, Jooeun Lee, Jong Kook Rhim, Heung Cheol Kim, Jin Pyeong Jeon

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  18. Toll-Like Receptor 2 Modulates Pulmonary Inflammation and TNF-α Release Mediated byFrontiers in cellular and infection microbiology · 2022
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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 3 institutions in 1 country.

Dong Hyuk Youn *Institute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Youngmi Kim *Institute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Bong Jun KimInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Myeong Seon JeongChuncheon Center, Korea Basic Science Institute, Chuncheon, Korea.
Jooeun LeeChuncheon Center, Korea Basic Science Institute, Chuncheon, Korea.
Jong Kook RhimDepartment of Neurosurgery, Jeju National University College of Medicine, Jeju, Korea.
Heung Cheol KimDepartment of Radioilogy, Hallym University College of Medicine, Chuncheon, Korea.
Jin Pyeong JeonDepartment of Neurosurgery, Hallym University College of Medicine, 77 Sakju-ro, Chuncheon, 24253, Republic of Korea. jjs6553@daum.net.
Hallym University · KRKorea Basic Science Institute · KRJeju National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decreased mitochondrial membrane potential in cerebrospinal fluid (CSF) was observed in patients with subarachnoid hemorrhage (SAH) accompanied by delayed cerebral ischemia (DCI). However, whether abnormal mechanisms of mitochondria are associated with the development of DCI has not been reported yet. Under cerebral ischemia, mitochondria can transfer into the extracellular space. Mitochondrial dysfunction can aggravate neurologic complications. The objective of this study was to evaluate whether mitochondrial dysfunction might be associated with autophagy and mitophagy in CSF cells to provide possible insight into DCI pathogenesis. CSF samples were collected from 56 SAH patients (DCI, n = 21; and non-DCI, n = 35). We analyzed CSF cells using autophagy and mitophagy markers (DAPK1, BNIP3L, BAX, PINK1, ULK1, and NDP52) via qRT-PCR and western blotting of proteins (BECN1, LC3, and p62). Confocal microscopy and immunogold staining were performed to demonstrate the differentially expression of markers within dysfunctional mitochondria. Significant induction of autophagic flux with accumulation of autophagic vacuoles, increased expression of BECN1, LC3-II, and p62 degradation were observed during DCI. Compared to non-DCI patients, DCI patients showed significantly increased mRNA expression levels (2

Indexed as

AutophagyMitophagyBrain IschemiaCerebrospinal FluidFemaleHumansMaleMembrane Potential, MitochondrialMicroscopy, Electron, TransmissionMiddle AgedMitochondriaSubarachnoid Hemorrhage

Identifiers

PMID34389795
PMCPMC8363614
OpenAlexW3188016912

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.