Evidence map›Paper›PMID 35267136›Full record

ArticleMetabolic brain disease2022

Potential of nobiletin against Alzheimer's disease through inhibiting neuroinflammation.

Wen Chai, Ji Zhang, Zhengbing Xiang, Honglian Zhang, Zhujun Mei, Hongbing Nie, Renxu Xu, Ping Zhang

Abstract read
PubMed Publisher
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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.5field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 27 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.

Wen ChaiDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China.
Ji ZhangDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China.
Zhengbing XiangDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China.
Honglian ZhangDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China.
Zhujun MeiDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China.
Hongbing NieDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China.
Renxu XuDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China.
Ping ZhangDepartment of Neurology, The First Affiliated Hospital of Nanchang Medical College/Jaingxi Provincial People's Hospital, No.152, Aiguo Road, 330006, Nanchang, Jiangxi, P.R. China. zhangkiki5201@163.com.
First Affiliated Hospital of Jiangxi Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to explore the mechanism of Nobiletin attenuating Alzheimer's disease (AD) by inhibiting neuroinflammation.

methodsThe expression of inflammatory cytokines and HMGB-1 in serum of AD patients were examined. Microglia (MGs) were treated with different doses of Nobiletin before LPS and Nigericin induction. Cell viability and apoptosis were determined by CCK-8 and TUNEL assays, respectively. APP/PS1 mice were gavaged with Nobiletin, and Morris water maze (MWM) was established to record swimming speed, escape latency, the number of platform crossings, and time spent in the platform quadrant. MGs activation in brain tissues was evaluated by immunofluorescence. The expression of pyroptosis-related proteins, inflammatory cytokines, and HMGB-1 was determined in the hippocampus and MGs.

resultsThe levels of inflammatory cytokines and HMGB-1 were high in serum of AD patients. Treatment with different concentrations of Nobiletin prominently enhanced cell viability and reduced apoptosis and the expression of inflammatory cytokine and pyroptosis-related proteins in LPS + Nigericin-induced MGs. Gavage of different doses of Nobiletin into APP/PS1 mice shortened the escape latency in mice, diminished MGs activation in brain tissues, and remarkably elevated the number of platform crossings and the time spent in the platform quadrant without obvious change in swimming speed, suggesting that Nobiletin improved the spatial learning and memory abilities in APP/PS1 mice. The expression of pyroptosis-related proteins, HMGB-1, and inflammatory cytokines was decreased dramatically by Nobiletin in the hippocampus of APP/PS1 mice.

conclusionsNobiletin can inhibit neuroinflammation by inhibiting HMGB-1, pyroptosis-related proteins, and inflammatory cytokines, thus mitigating AD.

Indexed as

Alzheimer DiseaseAnimalsCytokinesDisease Models, AnimalFlavonesHMGB ProteinsHumansLipopolysaccharidesMiceMice, TransgenicNeuroinflammatory DiseasesNigericinCytokinesFlavonesHMGB ProteinsLipopolysaccharidesNigericinnobiletinAlzheimer’s diseaseHMGB-1Inflammatory cytokinesNeuroinflammationNobiletinPyroptosis

Identifiers

PMID35267136
OpenAlexW4221096333

What OpenQuestion holds

Textmetadata
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.