Evidence map›Paper›PMID 39497351›Full record

ArticleClinical and experimental dental research2024

Experimental Periodontitis Increases Anxious Behavior and Worsens Cognitive Aspects and Systemic Oxidative Stress in Wistar Rats.

Giselle B de Castro, Ramona R S Pereira, Caíque O Diniz E Magalhães, Karine B Costa, Etel R Vieira, Ricardo C Cassilhas, Kinulpe H Sampaio, Alan R T Machado, Jaqueline do Carmo L Carvalho, Ramiro M Murata and 4 more

Abstract read
In one paragraph

Article in Clinical and experimental dental research, 2024. 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. Review
  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

14 authors.

Giselle B de CastroHealth Sciences Program, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0009-0006-5767-7866
Ramona R S PereiraHealth Sciences Program, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0009-0006-6971-2366
Caíque O Diniz E MagalhãesBiological and Health Sciences Department, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0000-0001-7440-5463
Karine B CostaHealth Sciences Program, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0000-0002-3383-3995
Etel R VieiraHealth Sciences Program, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0000-0001-6908-7237
Ricardo C CassilhasHealth Sciences Program, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0000-0001-6970-2551
Kinulpe H SampaioHealth Sciences Program, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0000-0002-8154-9606
Alan R T MachadoDepartment of Exact Sciences, Universidade do Estado de Minas Gerais, João Monlevade, Minas Gerais, Brazil.ORCID 0000-0002-4803-4600
Jaqueline do Carmo L CarvalhoDepartment of Exact Sciences, Universidade do Estado de Minas Gerais, João Monlevade, Minas Gerais, Brazil.ORCID 0000-0003-1937-4988
Ramiro M MurataDepartment of Foundational Sciences, School of Dental Medicine, East Carolina University (ECU), Greenville, North Carolina, USA.ORCID 0000-0002-8478-6981
Luciano J PereiraDepartment of Health Sciences, Universidade Federal de Lavras (UFLA), Lavras, Brazil.ORCID 0000-0002-0502-2554
Marco F Dias-PeixotoHealth Sciences Program, Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Diamantina, Minas Gerais, Brazil.ORCID 0000-0003-3324-3634
Eric F AndradeDepartment of Health Sciences, Universidade Federal de Lavras (UFLA), Lavras, Brazil.ORCID 0000-0002-9253-3108
Vanessa PardiDepartment of Foundational Sciences, School of Dental Medicine, East Carolina University (ECU), Greenville, North Carolina, USA.ORCID 0000-0001-7120-4332

Funding

The authors would like to thank the Research Support Foundation of the State of Minas Gerais (Fundação de Amparo à Pesquisa do Estado de Minas Gerais-FAPEMIG [Grant number: APQ-00583-21]), National Council for Scientific and Technological Development (Conselho Nacional de Desenvolvimento Científico e Tecnológico-CNPq), Coordination for the Improvement of Higher Education Personnel (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior-CAPES), and East Carolina University.
6 · The paper itself

Abstract

objectivesPeriodontitis (PD) has the potential to induce systemic changes that affect both physical and behavioral aspects. These alterations may be associated with changes in both the inflammatory profile and the oxidative stress status of individuals with PD. Therefore, we aimed to evaluate the effects of PD on oxidative stress, as well as on behavioral parameters and cognitive impairment, in a preclinical model. MATERIAL AND

methodsTwenty-four male Wistar rats were randomly assigned to PD and sham groups. PD was induced by the ligature protocol for 14 days. Behavioral tests were initiated on the 9th day of the experiment to evaluate anxious behavior and cognition (learning and memory). After euthanasia, oxidative stress was evaluated in the gums, blood, hippocampus, and amygdala. Alveolar bone loss, bone microstructure, and elemental compositions of the mandibular bone were also assessed.

resultsPD increased alveolar bone loss, reduced the calcium and phosphorus content in the mandibular bone, and increased anxiety-like behavior and cognitive decline (p < 0.05). Furthermore, PD significantly affected the redox balance, as evidenced by increased total antioxidant capacity (TAC) in the gingiva and hippocampus (p < 0.05). It also led to increased lipid peroxidation in the gingiva and erythrocytes (p < 0.05), decreased antioxidant defenses in erythrocytes (superoxide dismutase) and the hippocampus (catalase), and increased antioxidant activity (catalase) in the amygdala (p < 0.05).

conclusionPD resulted in cognitive alterations, including impairments in spatial learning and memory, as well as increased anxious behavior, likely due to redox imbalance in rats.

Indexed as

AnxietyBehavior, AnimalDisease Models, AnimalOxidative StressPeriodontitisRats, WistarAlveolar Bone LossAnimalsAntioxidantsCognitionCognitive DysfunctionGingivaHippocampusLipid PeroxidationMaleRatsAntioxidantsanxietycognitionoxidative stressperiodontal disease

Identifiers

PMID39497351
PMCPMC11534646

What OpenQuestion holds

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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.