Evidence map›Paper›PMID 35683023›Full record

ReviewInternational journal of molecular sciences2022

The Sedentary Lifestyle and Masticatory Dysfunction: Time to Review the Contribution to Age-Associated Cognitive Decline and Astrocyte Morphotypes in the Dentate Gyrus.

Fabíola de Carvalho Chaves de Siqueira Mendes, Marina Negrão Frota de Almeida, Manoela Falsoni, Marcia Lorena Ferreira Andrade, André Pinheiro Gurgel Felício, Luisa Taynah Vasconcelos Barbosa da Paixão, Fábio Leite do Amaral Júnior, Daniel Clive Anthony, Dora Brites, Cristovam Wanderley Picanço Diniz and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. 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
0.8field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

11 authors at 4 institutions in 3 countries.

Fabíola de Carvalho Chaves de Siqueira MendesLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.
Marina Negrão Frota de AlmeidaLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.
Manoela FalsoniLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.
Marcia Lorena Ferreira AndradeLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.
André Pinheiro Gurgel FelícioLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.
Luisa Taynah Vasconcelos Barbosa da PaixãoLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.
Fábio Leite do Amaral JúniorLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.ORCID 0000-0003-2755-2801
Daniel Clive AnthonyLaboratory of Experimental Neuropathology, Department of Pharmacology, University of Oxford, Oxford OX1 3QT, UK.ORCID 0000-0003-1380-6655
Dora BritesResearch Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, 1649-004 Lisbon, Portugal.ORCID 0000-0002-3024-9777
Cristovam Wanderley Picanço DinizLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.ORCID 0000-0001-6611-6880
Marcia Consentino Kronka SosthenesLaboratório de Investigações em Neurodegeneração e Infecção, Instituto de Ciências Biológicas, Hospital Universitário João de Barros Barreto, Universidade Federal do Pará, Belém 66073-005, PA, Brazil.
Universidade Federal do Pará · BRCentro Universitário do Pará · BRUniversity of Lisbon · PTUniversity of Oxford · GB

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior Bolsa Pós-GraduandoFundação Amazônia Paraense de Amparo à Pesquisa FAPESPA 136/08Fundação de Amparo e Desenvolvimento da Pesquisa FADESP/UFPA Editing and Publication FeesFundação para a Ciência e a Tecnologia Projects PTDC/MED-NEU/31395/2017, LISBOA-01-0145-FEDER-031395 and PTDC/MED-NEU/2382/2021iMed.ULisboa part UID/DTP/04138/2019-2021"la Caixa" Foundation HR21-00931National Council for Scientific and Technological Development 47677/2008-0Pró-Reitoria de Pesquisa e Pós-Graduação PROPESP/UFPA Editing and Publication fees
6 · The paper itself

Abstract

As aging and cognitive decline progresses, the impact of a sedentary lifestyle on the appearance of environment-dependent cellular morphologies in the brain becomes more apparent. Sedentary living is also associated with poor oral health, which is known to correlate with the rate of cognitive decline. Here, we will review the evidence for the interplay between mastication and environmental enrichment and assess the impact of each on the structure of the brain. In previous studies, we explored the relationship between behavior and the morphological features of dentate gyrus glial fibrillary acidic protein (GFAP)-positive astrocytes during aging in contrasting environments and in the context of induced masticatory dysfunction. Hierarchical cluster and discriminant analysis of GFAP-positive astrocytes from the dentate gyrus molecular layer revealed that the proportion of AST1 (astrocyte arbors with greater complexity phenotype) and AST2 (lower complexity) are differentially affected by environment, aging and masticatory dysfunction, but the relationship is not straightforward. Here we re-evaluated our previous reconstructions by comparing dorsal and ventral astrocyte morphologies in the dentate gyrus, and we found that morphological complexity was the variable that contributed most to cluster formation across the experimental groups. In general, reducing masticatory activity increases astrocyte morphological complexity, and the effect is most marked in the ventral dentate gyrus, whereas the effect of environment was more marked in the dorsal dentate gyrus. All morphotypes retained their basic structural organization in intact tissue, suggesting that they are subtypes with a non-proliferative astrocyte profile. In summary, the increased complexity of astrocytes in situations where neuronal loss and behavioral deficits are present is counterintuitive, but highlights the need to better understand the role of the astrocyte in these conditions.

Indexed as

AstrocytesCognitive DysfunctionAgingDentate GyrusGlial Fibrillary Acidic ProteinHippocampusHumansSedentary BehaviorGlial Fibrillary Acidic Proteinagingastrocyte morphometrycognitive declinedentate gyrusenvironmentmastication

Identifiers

PMID35683023
PMCPMC9180988
OpenAlexW4281697513

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.