Evidence map›Paper›PMID 34924995›Full record

ArticleFrontiers in aging neuroscience2021

Senescence in Primary Rat Astrocytes Induces Loss of the Mitochondrial Membrane Potential and Alters Mitochondrial Dynamics in Cortical Neurons.

Sandra Lizbeth Morales-Rosales, Roberto Santín-Márquez, Pedro Posadas-Rodriguez, Ruth Rincon-Heredia, Teresa Montiel, Raúl Librado-Osorio, Armando Luna-López, Nadia Alejandra Rivero-Segura, Claudio Torres, Agustina Cano-Martínez and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

15 authors at 6 institutions in 2 countries.

Sandra Lizbeth Morales-RosalesPosgrado Biología Experimental, Universidad Autónoma Metropolitana, Mexico City, Mexico.
Roberto Santín-MárquezPosgrado Biología Experimental, Universidad Autónoma Metropolitana, Mexico City, Mexico.
Pedro Posadas-RodriguezPosgrado Biología Experimental, Universidad Autónoma Metropolitana, Mexico City, Mexico.
Ruth Rincon-HerediaInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Teresa MontielInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Raúl Librado-OsorioDepartamento de Investigación Básica, Instituto Nacional de Geriatría, Mexico City, Mexico.
Armando Luna-LópezDepartamento de Investigación Básica, Instituto Nacional de Geriatría, Mexico City, Mexico.
Nadia Alejandra Rivero-SeguraDepartamento de Investigación Básica, Instituto Nacional de Geriatría, Mexico City, Mexico.
Claudio TorresDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, United States.
Agustina Cano-MartínezDepartamento de Fisiología, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Alejandro Silva-PalaciosDepartamento de Biomedicina Cardiovascular, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Paulina Cortés-HernándezInstituto Mexicano del Seguro Social, Centro de Investigación Biomédica de Oriente, Atlixco, Mexico.
Julio MoránInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Lourdes MassieuInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Mina KonigsbergDepartamento de Ciencias de la Salud, Universidad Autónoma Metropolitana, Mexico City, Mexico.
Universidad Autónoma Metropolitana · MXUniversidad Nacional Autónoma de México · MXInstituto Nacional de Pediatria · MXInstituto Nacional de Cardiología · MXDrexel University · USMexican Social Security Institute · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The decline in brain function during aging is one of the most critical health problems nowadays. Although senescent astrocytes have been found in old-age brains and neurodegenerative diseases, their impact on the function of other cerebral cell types is unknown. The aim of this study was to evaluate the effect of senescent astrocytes on the mitochondrial function of a neuron. In order to evaluate neuronal susceptibility to a long and constant senescence-associated secretory phenotype (SASP) exposure, we developed a model by using cellular cocultures in transwell plates. Rat primary cortical astrocytes were seeded in transwell

Indexed as

agingastrocytecellular senescencemitochondriaredox state

Identifiers

PMID34924995
PMCPMC8672143
OpenAlexW3217592219

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.