Evidence map›Paper›PMID 37005970›Full record

ReviewPharmacological reports : PR2023

Potential drugs for the treatment of Alzheimer's disease.

Tania Guadalupe Montero-Cosme, Luz Irene Pascual-Mathey, María Elena Hernández-Aguilar, Deissy Herrera-Covarrubias, Fausto Rojas-Durán, Gonzalo Emiliano Aranda-Abreu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pharmacological reports : PR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Marine-derived Compounds: A Powerful Platform for the Treatment of Alzheimer's Disease.Central nervous system agents in medicinal chemistry · 2024
    Review
  2. Review
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

6 authors at 1 institution in 1 country.

Tania Guadalupe Montero-CosmeFacultad de Química, Universidad Veracruzana, Xalapa, Veracruz, México.
Luz Irene Pascual-MatheyFacultad de Química, Universidad Veracruzana, Xalapa, Veracruz, México.ORCID http://orcid.org/0000-0001-5150-3140
María Elena Hernández-AguilarInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, Veracruz, México.ORCID http://orcid.org/0000-0002-1617-5636
Deissy Herrera-CovarrubiasInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, Veracruz, México.ORCID http://orcid.org/0000-0001-5752-4700
Fausto Rojas-DuránInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, Veracruz, México.ORCID http://orcid.org/0000-0003-4497-0909
Gonzalo Emiliano Aranda-AbreuInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, Veracruz, México. garanda@uv.mx.ORCID http://orcid.org/0000-0001-8519-5473
Universidad Veracruzana · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well known that amyloid precursor protein (APP), the enzyme β-secretase 1 (BACE1), cyclooxygenase 2 (COX-2), nicastrin (NCT), and hyperphosphorylated tau protein (p-tau) are closely related to the development of Alzheimer's disease (AD). In addition, recent evidence shows that neuroinflammation also contributes to the pathogenesis of AD. Although the mechanism is not clearly known, such inflammation could alter the activity of the aforementioned molecules. Therefore, the use of anti-inflammatory agents could slow the progression of the disease. Nimesulide, resveratrol, and citalopram are three anti-inflammatory agents that could contribute to a decrease in neuroinflammation and consequently to a decrease in the overexpression of APP, BACE1, COX-2, NCT, and p-Tau, as they possess anti-inflammatory effects that could regulate the expression of APP, BACE1, COX-2, NCT, and p-Tau of potent pro-inflammatory markers indirectly involved in the expression of APP, BACE1, NCT, COX-2, and p-Tau; therefore, their use could be beneficial as preventive treatment as well as in the early stages of AD.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesCyclooxygenase 2HumansNeuroinflammatory DiseasesAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesCyclooxygenase 2Alzheimer’s diseaseAPPBACE1COX-2InflammationNCTp-Tau

Identifiers

PMID37005970
OpenAlexW4362507183

What Socratic 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 Socratic graph.