Evidence map›Paper›PMID 41284069›Full record

ArticlePsychopharmacology2026

Sex-dependent therapeutic effects of nano-curcumin on alzheimer's disease: enhanced cognitive and physiological restoration in female mice.

Karline da Costa Rodrigues, Meliza da Conceição Oliveira, Isadora Cielo de Souza, Andreza Wachholz Igansi, Ana Vitória Barbosa Lopes, Camila de Oliveira Pacheco, Sandra Elisa Hass, Ricardo Frederico Schumacher, Cristiane Luchese

Abstract read
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In one paragraph

Article in Psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Karline da Costa RodriguesPrograma de Pós-graduação em Bioquímica e Bioprospecção, Grupo de Pesquisa em Neurobiotecnologia (GPN), Centro de Ciências Químicas, Farmacêuticas e de Alimentos, Universidade Federal de Pelotas (UFPel), Pelotas, RS, CEP 96010-900, Brasil.ORCID http://orcid.org/0000-0003-2495-2252
Meliza da Conceição OliveiraPrograma de Pós-graduação em Bioquímica e Bioprospecção, Grupo de Pesquisa em Neurobiotecnologia (GPN), Centro de Ciências Químicas, Farmacêuticas e de Alimentos, Universidade Federal de Pelotas (UFPel), Pelotas, RS, CEP 96010-900, Brasil.ORCID http://orcid.org/0000-0002-0320-141X
Isadora Cielo de SouzaPrograma de Pós-graduação em Bioquímica e Bioprospecção, Grupo de Pesquisa em Neurobiotecnologia (GPN), Centro de Ciências Químicas, Farmacêuticas e de Alimentos, Universidade Federal de Pelotas (UFPel), Pelotas, RS, CEP 96010-900, Brasil.ORCID http://orcid.org/0009-0004-4883-6648
Andreza Wachholz IgansiPrograma de Pós-graduação em Bioquímica e Bioprospecção, Grupo de Pesquisa em Neurobiotecnologia (GPN), Centro de Ciências Químicas, Farmacêuticas e de Alimentos, Universidade Federal de Pelotas (UFPel), Pelotas, RS, CEP 96010-900, Brasil.ORCID http://orcid.org/0009-0004-1676-845X
Ana Vitória Barbosa LopesPrograma de Pós-graduação em Bioquímica e Bioprospecção, Grupo de Pesquisa em Neurobiotecnologia (GPN), Centro de Ciências Químicas, Farmacêuticas e de Alimentos, Universidade Federal de Pelotas (UFPel), Pelotas, RS, CEP 96010-900, Brasil.ORCID http://orcid.org/0009-0009-2606-1702
Camila de Oliveira PachecoPrograma de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Pampa, Campus Uruguaiana BR 472, Km 7, Uruguaiana, RS, 97500-970, Brasil.ORCID http://orcid.org/0000-0002-0689-4952
Sandra Elisa HassPrograma de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Pampa, Campus Uruguaiana BR 472, Km 7, Uruguaiana, RS, 97500-970, Brasil.ORCID http://orcid.org/0000-0002-5687-6736
Ricardo Frederico SchumacherDepartamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105- 900, Brazil.ORCID http://orcid.org/0000-0003-4723-1925
Cristiane LuchesePrograma de Pós-graduação em Bioquímica e Bioprospecção, Grupo de Pesquisa em Neurobiotecnologia (GPN), Centro de Ciências Químicas, Farmacêuticas e de Alimentos, Universidade Federal de Pelotas (UFPel), Pelotas, RS, CEP 96010-900, Brasil. cristiane_luchese@yahoo.com.br.ORCID http://orcid.org/0000-0001-6001-0532

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 160674/2020-4Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul PqG 24/2551-0001249-4
6 · The paper itself

Abstract

Curcumin (Cur) is a bioactive compound with neuroprotective and anti-inflammatory effects, though its clinical application is limited by poor bioavailability. This study assessed the impact of nanocapsulated curcumin (NcCur), formulated Eudragit (EUD) polymer, in a sporadic Alzheimer's disease (AD) mouse model induced by intracerebroventricular streptozotocin (STZ), with attention to sex-specific differences. Mice received STZ (3 nmol/3 µL) or 0.9% saline on days 1 and 3, followed by intragastric treatment with Cur or NcCur (10 mg/kg, on alternate days) from day 22 until euthanasia - a dose previously shown to be effective in behavioral and biochemical modulation in rodent models of neurodegeneration. Behavioral assessments included open field, elevated plus maze (EPM), tail suspension (TST), object recognition, Y-maze, and step-down avoidance tasks (SDAT), performed before and after treatment. After euthanasia, thymus, spleen and adrenal glands were weighed; biochemical assays evaluated oxidative stress, monoaminergic and cholinergic enzymes, and Na⁺K⁺-ATPase activity. NcCur improved short- and long-term memory in both sexes, with greater effects in females (42% and 35%) than males (28% and 25%). In the EPM, NcCur increased open arm time more prominently in females (40%) than males (25%), while TST immobility time was reduced similarly in both. Spatial and aversive memory improved in both sexes, but females showed greater performance in the SDAT. Biochemical analyses showed reductions in reactive species in males (45%) and females (55%) with NcCur; Na⁺K⁺-ATPase activity increased in females (60%) and males (50%). AChE activity was restored in both sexes. NcCur reduced MAO-A/B activities more in females (65%/55%) than in males (45%/35%). Thymus and spleen weights were normalized in both sexes, with stronger effects in females. NcCur also mitigated alterations in thymus and spleen relative weights, suggesting immunomodulatory effects. Some biochemical and behavioral responses were more prominent in females, both sexes benefited from treatments. These findings suggest that NcCur enhances Cur therapeutic potential through multimodal actions linked involving modulation of oxidative stress, cholinergic and monoaminergic systems, and immune-related parameters. NcCur emerges as a promising candidate for AD-like intervention in both sexes.

Indexed as

Alzheimer DiseaseCognitionCurcuminAnimalsBehavior, AnimalDisease Models, AnimalFemaleMaleMaze LearningMemoryMiceNeuroprotective AgentsOxidative StressSex CharacteristicsSex FactorsSodium-Potassium-Exchanging ATPaseCurcuminNeuroprotective AgentsSodium-Potassium-Exchanging ATPaseStreptozocinAnxious-likeCurcuma longaDepression-likeMemoryNanocapsules

Identifiers

PMID41284069

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.