Evidence map›Paper›PMID 24972270›Full record

ArticleMolecules (Basel, Switzerland)2014

Regulatory effects of fisetin on microglial activation.

Jing-Yuan Chuang, Pei-Chun Chang, Yi-Chun Shen, Chingju Lin, Cheng-Fang Tsai, Jia-Hong Chen, Wei-Lan Yeh, Ling-Hsuan Wu, Hsiao-Yun Lin, Yu-Shu Liu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 57 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 5 institutions in 1 country.

Jing-Yuan ChuangDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 40402, Taiwan. jychuang@mail.cmu.edu.tw.
Pei-Chun ChangDepartment of Bioinformatics, Asia University, Taichung 41354, Taiwan. pcchang@asia.edu.tw.
Yi-Chun ShenDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 40402, Taiwan. syciac@gmail.com.
Chingju LinDepartment of Physiology, School of Medicine, China Medical University, Taichung 40402, Taiwan. clin33@mail.cmu.edu.tw.
Cheng-Fang TsaiDepartment of Biotechnology, Asia University, Taichung 41354, Taiwan. tsaicf@asia.edu.tw.
Jia-Hong ChenDepartment of General Surgery, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taichung 42743, Taiwan. guns5150@ms27.hinet.net.
Wei-Lan YehDepartment of Cell and Tissue Engineering, Changhua Christian Hospital, Changhua 500, Taiwan. ibizayeh0816@hotmail.com.
Ling-Hsuan WuGraduate Institute of Basic Medical Science, China Medical University, Taichung 40402, Taiwan. lulu80620@yahoo.com.tw.
Hsiao-Yun LinDepartment of Life Sciences, National Chung Hsing University, Taichung 402, Taiwan. lingirl831@hotmail.com.
Yu-Shu LiuGraduate Institute of Basic Medical Science, China Medical University, Taichung 40402, Taiwan. yushuliu220@gmail.com.
Dah-Yuu LuGraduate Institute of Neural and Cognitive Sciences, China Medical University, Taichung 40402, Taiwan. dahyuu@mail.cmu.edu.tw.
China Medical University · TWAsia University · TWChanghua Christian Hospital · TWNational Chung Hsing University · TWTaipei Tzu Chi Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence suggests that inflammatory processes in the central nervous system that are mediated by microglial activation play a key role in neurodegeneration. Fisetin, a plant flavonol commonly found in fruits and vegetables, is frequently added to nutritional supplements due to its antioxidant properties. In the present study, treatment with fisetin inhibited microglial cell migration and ROS (reactive oxygen species) production. Treatment with fisetin also effectively inhibited LPS plus IFN-γ-induced nitric oxide (NO) production, and inducible nitric oxide synthase (iNOS) expression in microglial cells. Furthermore, fisetin also reduced expressions of iNOS and NO by stimulation of peptidoglycan, the major component of the Gram-positive bacterium cell wall. Fisetin also inhibited the enhancement of LPS/IFN-γ- or peptidoglycan-induced inflammatory mediator IL (interlukin)-1 β expression. Besides the antioxidative and anti-inflammatory effects of fisetin, our study also elucidates the manner in fisetin-induced an endogenous anti-oxidative enzyme HO (heme oxygenase)-1 expression. Moreover, the regulatory molecular mechanism of fisetin-induced HO-1 expression operates through the PI-3 kinase/AKT and p38 signaling pathways in microglia. Notably, fisetin also significantly attenuated inflammation-related microglial activation and coordination deficit in mice in vivo. These findings suggest that fisetin may be a candidate agent for the development of therapies for inflammation-related neurodegenerative diseases.

Indexed as

AnimalsAnti-Inflammatory AgentsCell LineCell MovementDrug Evaluation, PreclinicalFlavonoidsFlavonolsHeme Oxygenase-1LipopolysaccharidesMaleMembrane ProteinsMice, Inbred ICRMicrogliaNeuroprotective AgentsNitric OxideNitric Oxide Synthase Type IIAnti-Inflammatory AgentsfisetinFlavonoidsFlavonolsHeme Oxygenase-1Hmox1 protein, mouseLipopolysaccharidesMembrane ProteinsNeuroprotective AgentsNitric OxideNitric Oxide Synthase Type IINos2 protein, mouseReactive Oxygen Species

Identifiers

PMID24972270
PMCPMC6271444
OpenAlexW2130719413

What OpenQuestion holds

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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 OpenQuestion graph.