Evidence map›Paper›PMID 35976554›Full record

ArticleMetabolic brain disease2022

Salidroside inhibited cerebral ischemia/reperfusion-induced oxidative stress and apoptosis via Nrf2/Trx1 signaling pathway.

Fuyuan Li, Qianqian Mao, Jinyu Wang, Xiaoying Zhang, Xinyan Lv, Bo Wu, Tingxu Yan, Ying Jia

Abstract read
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In one paragraph

Article in Metabolic brain disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 35 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.

Fuyuan LiSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
Qianqian MaoSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
Jinyu WangSchool of Functional Food and Wine, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, China.
Xiaoying ZhangSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
Xinyan LvSchool of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
Bo WuSchool of Functional Food and Wine, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, China.
Tingxu YanSchool of Functional Food and Wine, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, China. yantingxu@126.com.
Ying JiaSchool of Functional Food and Wine, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, China. jiayingsyphu@126.com.ORCID 0000-0002-1289-4350
Shenyang Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral ischemia reperfusion injury (CIRI) is still a serious problem threatening human health. Salidroside (SAL) is a natural phenylpropanoid glycoside compound with antioxidant, anti-inflammatory, and anti-ischemic properties. This study investigated the protective mechanism of SAL on middle cerebral artery occlusion (MCAO)- and oxygen-glucose deprivation/reoxygenation (OGD/R) model-induced CIRI via regulating the nuclear factor erythroid 2-related factor 2 (Nrf2)/thioredoxin 1 (Trx1) axis. The results indicated that SAL (50 mg/kg or 100 mg/kg, intraperitoneal injection) not only effectively alleviated infarction rate, improved histopathological changes, relieved apoptosis by strengthening the suppression of cleaved caspase-3 and Bax/Bcl-2 proteins and decreased malondialdehyde (MDA) formation, but also increased superoxide dismutase (SOD) and catalase (CAT) activities and upregulated the expressions of Nrf2 and Trx1 on MCAO-induced CIRI rats. SAL also efficiently inhibited apoptosis and decreased oxidative stress in OGD/R-stimulated PC12 cells. Furthermore, blocking the Nrf2/Trx1 pathway using tretinoin, an Nrf2 inhibitor, significantly reversed the protective effect of SAL on OGD/R-induced oxidative stress. Moreover, SAL reduced the expression of apoptosis signal-regulating kinase-1 (ASK1) and mitogen-activated protein kinase (MAPK) family proteins. These results demonstrated that SAL inhibited oxidative stress through Nrf2/Trx1 signaling pathway, and subsequently reduced CIRI-induced apoptosis by inhibiting ASK1/MAPK.

Indexed as

Brain IschemiaReperfusion InjuryAnimalsAntioxidantsApoptosisGlucosidesHumansInfarction, Middle Cerebral ArteryMitogen-Activated Protein KinasesNF-E2-Related Factor 2Oxidative StressPhenolsRatsReperfusionSignal TransductionThioredoxinsAntioxidantsGlucosidesMitogen-Activated Protein KinasesNF-E2-Related Factor 2PhenolsrhodiolosideThioredoxinsApoptosisCerebral ischemia/reperfusionNrf2/Trx1Oxidative stressSalidroside

Identifiers

PMID35976554
OpenAlexW4292080624

What OpenQuestion holds

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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.