Evidence map›Paper›PMID 41303425›Full record

ArticleInternational journal of molecular sciences2025

Temporal Progression of Recognition Memory Impairment, Astrogliosis, and Cholinergic Dysfunction in the Streptozotocin Rat Model of Sporadic Alzheimer's Disease.

Sofía Niño-Rivero, Rossana Cabral, Jazmín Fleitas, Lucía Alcalde-Ahlig, Eduardo M Castaño, Laura Morelli, Ronald McGregor, Pablo Galeano, Patricia Lagos

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Sofía Niño-RiveroUnidad Académica de Fisiología, Facultad de Medicina, Universidad de la República, Gral. Flores 2125, Montevideo 11800, Uruguay.ORCID 0000-0001-7663-3654
Rossana CabralUnidad Académica de Fisiología, Facultad de Medicina, Universidad de la República, Gral. Flores 2125, Montevideo 11800, Uruguay.
Jazmín FleitasUnidad Académica de Fisiología, Facultad de Medicina, Universidad de la República, Gral. Flores 2125, Montevideo 11800, Uruguay.
Lucía Alcalde-AhligUnidad Académica de Fisiología, Facultad de Medicina, Universidad de la República, Gral. Flores 2125, Montevideo 11800, Uruguay.
Eduardo M CastañoLaboratory of Brain Aging and Neurodegeneration, Fundación Instituto Leloir (IIBBA-CONICET), Av. Patricias Argentinas 435, Ciudad Autónoma de Buenos Aires C1405BWE, Argentina.
Laura MorelliLaboratory of Brain Aging and Neurodegeneration, Fundación Instituto Leloir (IIBBA-CONICET), Av. Patricias Argentinas 435, Ciudad Autónoma de Buenos Aires C1405BWE, Argentina.ORCID 0000-0001-5759-1807
Ronald McGregorNeuropsychiatric Institute and Brain Research Institute, University of California, Los Angeles, CA 90095, USA.ORCID 0000-0001-8856-7455
Pablo GaleanoLaboratory of Brain Aging and Neurodegeneration, Fundación Instituto Leloir (IIBBA-CONICET), Av. Patricias Argentinas 435, Ciudad Autónoma de Buenos Aires C1405BWE, Argentina.ORCID 0000-0003-4491-2039
Patricia LagosUnidad Académica de Fisiología, Facultad de Medicina, Universidad de la República, Gral. Flores 2125, Montevideo 11800, Uruguay.ORCID 0000-0002-3227-065X

Funding

Agencia Nacional de Innovación e Investigación (ANII) FCE_1_2017_1_136039
6 · The paper itself

Abstract

The streptozotocin (STZ) experimental model of sporadic Alzheimer's disease (SAD), the most prevalent form of this type of dementia, has become a valuable tool to study the behavioral and morphological changes that occur during the gradual development of this pathology. We used the STZ experimental model in combination with the novel object recognition test (NORT) and immunohistochemical techniques to evaluate the recognition memory decline and morphological alterations in memory-related structures (hippocampus and cortex). Our analysis included five different time points after intracerebroventricular (ICV) administration of 3 mg/kg of STZ or artificial cerebrospinal fluid (aCSF) as a control. The time points included three distinct stages: early (15 and 30 days), intermediate (60 days), and late (90 and 120 days). We found that recognition memory impairment started in the intermediate stage and persisted through the later stages. Morphologically, we detected significant astrogliosis starting in the early stages, whereas cholinergic changes began in the intermediate stage. No neuronal loss was observed at any of the time points analyzed. Our results further support the hypothesis that astrogliosis constitutes an initial pathological event that may compromise the hippocampal cholinergic system and can contribute to the onset of recognition memory deficits.

Indexed as

Alzheimer DiseaseGliosisMemory DisordersAnimalsDisease Models, AnimalDisease ProgressionHippocampusMaleRatsRats, WistarRecognition, PsychologyStreptozocinStreptozocinacetylcholineAlzheimer’s diseaseastrogliosishippocampusparietal cortexrecognition memorystreptozotocin

Identifiers

PMID41303425
PMCPMC12652115

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.