Evidence map›Paper›PMID 39302597›Full record

ArticleNeurochemical research2024

Ferulic Acid-Loaded Nanostructure Maintains Brain Levels of ACh, Glutamate, and GABA and Ameliorates Anxiety and Memory Impairments Induced by the D-Galactose Aging Process in Rats.

Domenika R Rossato, Jéssica L O Rosa, Murilo B Fontoura, Leana E M de Souza, Tielle M de Almeida, Kathiane B Kudrna, Scheila R Schaffazick, Cristiane B da Silva, Letícia Birk, Sarah Eller and 2 more

Abstract read
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In one paragraph

Article in Neurochemical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Enhancement of Cognitive Benefits and Anti-Anxiety Effects ofAntioxidants (Basel, Switzerland) · 2025
    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

12 authors.

Domenika R RossatoGraduation Program of Pharmacology, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brazil.
Jéssica L O RosaGraduation Program of Pharmacology, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brazil.
Murilo B FontouraGraduation Program of Pharmacology, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brazil.
Leana E M de SouzaDepartamento de Fisiologia e Farmacologia, UFSM, Santa Maria, RS, Brazil.
Tielle M de AlmeidaGraduation Program of Pharmaceutical Sciences, UFSM, Santa Maria, RS, Brazil.
Kathiane B KudrnaDepartamento de Farmácia, UFSM, Santa Maria, RS, Brazil.
Scheila R SchaffazickGraduation Program of Pharmaceutical Sciences, UFSM, Santa Maria, RS, Brazil.
Cristiane B da SilvaGraduation Program of Pharmaceutical Sciences, UFSM, Santa Maria, RS, Brazil.
Letícia BirkGraduation Program in Health Sciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Sarah EllerGraduation Program in Health Sciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Tiago F de OliveiraGraduation Program in Health Sciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.
Marilise E BurgerGraduation Program of Pharmacology, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brazil. marilise.burger@ufsm.br.

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2014/50928-2
6 · The paper itself

Abstract

Population aging is a global reality driven by increased life expectancy. This demographic phenomenon is intrinsically linked to the epidemic of cognitive disorders such as dementia and Alzheimer's disease, posing challenges for elderly and their families. In this context, the search for new therapeutic strategies to prevent or minimize cognitive impairments becomes urgent, as these deficits are primarily associated with oxidative damage and increased neuroinflammation. Ferulic acid (FA), a natural and potent antioxidant compound, is proposed to be nanoencapsulated to target the central nervous system effectively with lower doses and an extended duration of action. Here, we evaluated the effects of the nanoencapsulated FA on d-galactose (d-Gal)- induced memory impairments. Male Wistar adult rats were treated with ferulic acid-loaded nanocapsules (FA-Nc) or non-encapsulated ferulic acid (D-FA) for 8 weeks concurrently with d-Gal (150 mg/kg s.c.) injection. As expected, our findings showed that d-Gal injection impaired memory processes and increased anxiety behavior, whereas FA-Nc treatment ameliorated these behavioral impairments associated with the aging process induced by d-Gal. At the molecular level, nanoencapsulated ferulic acid (FA-Nc) ameliorated the decrease in ACh and glutamate induced by d-galactose (d-Gal), and also increased GABA levels in the dorsal hippocampus, indicating its therapeutic superiority. Additional studies are needed to elucidate the mechanisms underlying our current promising outcomes. Nanoscience applied to pharmacology can reduce drug dosage, thereby minimizing adverse effects while enhancing therapeutic response, particularly in neurodegenerative diseases associated with aging. Therefore, the strategy of brain-targeted drug delivery through nanoencapsulation can be effective in mitigating aging-related factors that may lead to cognitive deficits.

Indexed as

AgingAnxietyCoumaric AcidsGalactosegamma-Aminobutyric AcidGlutamic AcidMemory DisordersRats, WistarAnimalsBrainMaleNanocapsulesNanostructuresRatsCoumaric Acidsferulic acidGalactosegamma-Aminobutyric AcidGlutamic AcidNanocapsulesAging-processAntioxidant propertyMemory lossNanoencapsulated ferulic acid

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.