Evidence map›Paper›PMID 37897134›Full record

ArticleBrain and behavior2023

Seipin overexpression attenuates cerebral ischemia-reperfusion injury via preventing apoptosis and autophagy.

Xiaoxi Zhu, Xiaoqiong An, Ming Chen, Dongfen Guo, Peng Xie, Bi Wang, Zhi Huang, Wenfeng Yu

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

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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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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 1 institution in 1 country.

Xiaoxi ZhuKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.
Xiaoqiong AnKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.
Ming ChenKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.
Dongfen GuoKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.
Peng XieKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.
Bi WangKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.
Zhi HuangKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.
Wenfeng YuKey Laboratory of Molecular Biology, School of Basic Medical Science of Guizhou Medical University, Guiyang City, China.ORCID 0000-0002-0567-5643
Guiyang Medical University · CN

Funding

Guizhou Province Science and Technology Planning Project GuizhouGeneticBasis-ZK[2023]General326National Natural Science Foundation of China 82060232National Natural Science Foundation of China 82160225Science and Technology Department of Guizhou Province (2019) 4008Science and Technology Plan Project of Guizhou Province (2020)1Z060
6 · The paper itself

Abstract

backgroundIschemic cerebrovascular disease (ICVD) is one of three fatal diseases in humans, along with heart disease and malignant tumors. Cerebral ischemia/reperfusion injury (CI/RI) is the primary cause of ICVD. Recently, seipin was reported to be crucial for lipid droplet formation, hepatic steatosis, and axonal atrophy. However, the function and mechanism of seipin in CI/RI has not been explicitly stated.

methodsOxygen-glucose deprivation/reoxygenation (OGD/R) hippocampal neuron cell line (HT-22) and middle cerebral artery occlusion (MCAO) in rats were established. The levels of apoptosis- and autophagy-related proteins and seipin were confirmed by western blot. Cell proliferation was assessed with CCK-8, and ischemic infarction and pathological structure were monitored by TTC and H&E staining, and tissue apoptosis was assessed through TUNEL assay.

resultsThe proliferative activity was decreased, and apoptosis and autophagy pathways could also be induced in the OGD/R HT-22 cells. Seipin overexpression accelerated viability and inhibited apoptosis and autophagy in the OGD/R HT-22 cells. Moreover, the data revealed that seipin overexpression could also attenuate cerebral infarction, apoptosis. Autophagy pathways could be repressed by seipin in the MCAO rats.

conclusionSeipin has a protective role against CI/RI in rats, and its mechanism might be relevant to the suppression of apoptosis and autophagy, suggesting that seipin might be a latent target for CI/RI.

Indexed as

Brain IschemiaReperfusion InjuryAnimalsApoptosisAutophagyCell LineGlucoseGTP-Binding Protein gamma SubunitsHumansInfarction, Middle Cerebral ArteryOxygenOxygen RadioisotopesRatsBscl2 protein, ratGlucoseGTP-Binding Protein gamma SubunitsOxygenOxygen-22Oxygen RadioisotopesapoptosisautophagyCI/RIseipin

Identifiers

PMID37897134
PMCPMC10726895
OpenAlexW4387996529

What OpenQuestion holds

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LicenceCC BY
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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.