Evidence map›Paper›PMID 35807356›Full record

ArticleMolecules (Basel, Switzerland)2022

Protective Effects of Jujubosides on 6-OHDA-Induced Neurotoxicity in SH-SY5Y and SK-N-SH Cells.

Chao-Hsuan Chen, Pei-Chen Hsu, Shih-Wei Hsu, Kun-Ting Hong, Kai-Yuan Chen, Jie-Long He, Der-Yang Cho, Yun-Chi Wang, Wen-Shin Chang, Da-Tian Bau and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. 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 19% 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

6 citing papers in PubMed, 10 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

11 authors at 6 institutions in 1 country.

Chao-Hsuan ChenGraduate Institute of Biomedical Sciences, China Medical University, Taichung 404333, Taiwan.ORCID 0000-0002-5200-6653
Pei-Chen HsuDepartment of Pediatrics, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan 33004, Taiwan.
Shih-Wei HsuTaichung Armed Forces General Hospital, Taichung 41152, Taiwan.
Kun-Ting HongDepartment of Neurological Surgery, Tri-Service General Hospital, Taipei 11490, Taiwan.
Kai-Yuan ChenDepartment of Neurosurgery, Neurological Institute, Taichung Veterans General Hospital, Taichung 40705, Taiwan.
Jie-Long HeDepartment of Post-Baccalaureate Veterinary Medicine, Asia University, Taichung 41354, Taiwan.ORCID 0000-0002-4301-0829
Der-Yang ChoDepartment of Neurosurgery, China Medical University Hospital, Taichung 404333, Taiwan.
Yun-Chi WangGraduate Institute of Biomedical Sciences, China Medical University, Taichung 404333, Taiwan.
Wen-Shin ChangGraduate Institute of Biomedical Sciences, China Medical University, Taichung 404333, Taiwan.
Da-Tian BauGraduate Institute of Biomedical Sciences, China Medical University, Taichung 404333, Taiwan.ORCID 0000-0002-5504-8656
Chia-Wen TsaiGraduate Institute of Biomedical Sciences, China Medical University, Taichung 404333, Taiwan.
China Medical University · TWAsia University · TWMinistry of Health and Welfare · TWTaichung Armed Forces General Hospital · TWTaichung Veterans General Hospital · TWTri-Service General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

6-hydroxydopamine (6-OHDA) is used to induce oxidative damage in neuronal cells, which can serve as an experimental model of Parkinson's disease (PD). Jujuboside A and B confer free radical scavenging effects but have never been examined for their neuroprotective effects, especially in PD; therefore, in this study, we aimed to investigate the feasibility of jujubosides as protectors of neurons against 6-OHDA and the underlying mechanisms. 6-OHDA-induced neurotoxicity in the human neuronal cell lines SH-SY5Y and SK-N-SH, was used to evaluate the protective effects of jujubosides. These findings indicated that jujuboside A and B were both capable of rescuing the 6-OHDA-induced loss of cell viability, activation of apoptosis, elevation of reactive oxygen species, and downregulation of the expression levels of superoxide dismutase, catalase, and glutathione peroxidase. In addition, jujuboside A and B can reverse a 6-OHDA-elevated Bax/Bcl-2 ratio, downregulate phosphorylated PI3K and AKT, and activate caspase-3, -7, and -9. These findings showed that jujubosides were capable of protecting both SH-SY5Y and SK-N-SH neuronal cells from 6-OHDA-induced toxicity via the rebalancing of the redox system, together with the resetting of the PI3K/AKT apoptotic signaling cascade. In conclusion, jujuboside may be a potential drug for PD prevention.

Indexed as

NeuroblastomaNeuroprotective AgentsNeurotoxicity SyndromesApoptosisCell Line, TumorHumansOxidopaminePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen SpeciesNeuroprotective AgentsOxidopaminePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen Species6-hydroxydopamineapoptosiscaspasejujubosidesParkinson’s diseasereactive oxygen species

Identifiers

PMID35807356
PMCPMC9268520
OpenAlexW4283593807

What Socratic 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 Socratic graph.