Evidence map›Paper›PMID 40231522›Full record

ReviewCurrent neuropharmacology2025

Potential Benefits of Quercetin through P2X7 Modulation against Neuroinflammation in Alzheimer's Disease.

Matheus Chimelo Bianchini, Francini Franscescon, Adinei Abadio Soares, Vinicius Ansolin, Kailane Paula Pretto, Marcelo Lemos Vieira da Cunha, Debora Tavares de Resende E Silva

Abstract readReview
In one paragraph

Review in Current neuropharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Plants, Pills, and the Brain: Exploring Phytochemicals and Neurological Medicines.International journal of plant, animal and environmental sciences · 2025
    Article
  4. Article
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

7 authors.

Matheus Chimelo BianchiniGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.
Francini FranscesconGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.
Adinei Abadio SoaresMedicine Department, Federal University of Fronteira Sul, Chapecó, Santa Catarina, Brazil.
Vinicius AnsolinNursing Department, Federal University of Fronteira Sul, Chapecó, Santa Catarina, Brazil.
Kailane Paula PrettoNursing Department, Federal University of Fronteira Sul, Chapecó, Santa Catarina, Brazil.
Marcelo Lemos Vieira da CunhaDepartment of Neurosurgeon, Federal University of Fronteira Sul, Chapecó, Santa Catarina, Brazil.
Debora Tavares de Resende E SilvaGraduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease is the leading cause of dementia worldwide. It belongs to the group of neurodegenerative ailments caused by the accumulation of extracellular β-amyloid plaques (Aβ) and intracellular neurofibrillary tau tangles, which damage brain tissue. One of the mechanisms proposed involves protein neurotoxicity and neuroinflammation through the purinergic system pathway. Several endogenous nucleotides, such as Adenosine 5'-triphosphate (ATP), are involved in cell signaling. High ATP levels can cause P2X7 receptor hyper-stimulation, resulting in an exacerbated inflammatory process and in apoptosis of cells. From this perspective, searching for new therapies becomes important to assist in the patient's treatment and quality of life. As a flavonoid with several properties, including anti-inflammatory activity, Quercetin may be an alternative to alleviate the damage and symptoms caused by Alzheimer's disease. Therefore, this review aims to examine the potential of Quercetin through P2X7 modulation against neuroinflammation in Alzheimer's disease, as it affects the P2X7 receptor by direct and indirect interactions, resulting in decreased inflammation levels. Therefore, we believe that Quercetin may have significant power in modulating the P2X7 receptor, demonstrating that the purinergic system has the potential to modulate neuroinflammation and can add to the treatment, reduce disease progression, and result in better prognoses. Furthermore, technological alternatives such as Quercetin micronization might improve its delivery to target tissues.

Indexed as

Alzheimer DiseaseNeuroinflammatory DiseasesQuercetinReceptors, Purinergic P2X7AnimalsHumansQuercetinReceptors, Purinergic P2X7flavonoidsneuroinflammation.purinergic systemQuercetinTau hyperphosphorylationβ-Amyloid

Identifiers

PMID40231522
PMCPMC12606667

What OpenQuestion holds

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LicenceCC BY
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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.