Evidence map›Paper›PMID 40661259›Full record

ArticleTranslational neuroscience2025

Mechanism study on the attenuation of cerebral ischemia-reperfusion injury by LBP extract through regulation of SIRT1/PGC-1α axis.

Qingfeng Niu, Jiahui Peng, Yujia Zhou, Xiaowen Li, Ouya Liu, Cheng Xin, Ping Liu, Changchun Hei, Xiao Yang

Abstract read
In one paragraph

Article in Translational neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Bioactive spectrum of goji berries (Food chemistry: X · 2026
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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

9 authors.

Qingfeng NiuDepartment of Neurology, General Hospital of Ningxia Medical University, Yinchuan, China.ORCID https://orcid.org/0009-0006-2854-7376
Jiahui PengDepartment of Neurology, General Hospital of Ningxia Medical University, Yinchuan, China.
Yujia ZhouPeking University First Hospital-Ningxia Women Children Hospital, Yinchuan, China.
Xiaowen LiSchool of Basic Medicine, Ningxia Medical University, Yinchuan, China.
Ouya LiuDepartment of Endocrinology, General Hospital of Ningxia Medical University, Yinchuan, China.
Cheng XinDepartment of Endocrinology, General Hospital of Ningxia Medical University, Yinchuan, China.
Ping LiuDepartment of Endocrinology, General Hospital of Ningxia Medical University, Yinchuan, China.
Changchun HeiSchool of Basic Medicine, Ningxia Medical University, Yinchuan, China.
Xiao YangDepartment of Neurology, General Hospital of Ningxia Medical University, Yinchuan, China.ORCID https://orcid.org/0000-0003-3065-7225

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aims to determine if Methods: A cellular hypoxia/reoxygenation model (OGD/R) using HT22 cells was established to simulate cerebral ischemia-reperfusion injury. Cells were allocated into four groups: normal (Control), hypoxia (OGD/R), LBP extract-treated (OGD/R + LBP at 25, 50, 100 μg/mL), and SIRT1-inhibited (OGD/R + S100). Western blot and qPCR were performed to detect the expression of pathway-related factors, oxidative stress, mitochondrial function, and apoptosis-related factors. Results: Compared to the Control group, the OGD/R group exhibited significantly reduced cell survival, increased LDH release, apoptosis rate, and reactive oxygen species (ROS) levels. After intervention with LBP extract, cell survival increased, LDH release, ROS levels, and apoptosis rates reduced. The above injuries were associated with the inhibition of the SIRT1/PGC-1α pathway. LBP extract can attenuate the hypoxia-reperfusion-induced inhibition of the SIRT1/PGC-1α pathway and reverse the resulting high levels of oxidative stress and apoptosis, ultimately ameliorating cellular injury. Conclusion: LBP extract's protective effects against ischemia-reperfusion injury in HT22 cells appear linked to the modulation of the SIRT1/PGC-1α pathway and a reduction in oxidative stress.

Indexed as

hypoxia-reperfusionLBPoxidative stressPGC-1αROSSIRT1

Identifiers

PMID40661259
PMCPMC12258424

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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.