Evidence map›Paper›PMID 34336096›Full record

ArticleOxidative medicine and cellular longevity2021

Low-Intensity Exercise Routine for a Long Period of Time Prevents Osteosarcopenic Obesity in Sedentary Old Female Rats, by Decreasing Inflammation and Oxidative Stress and Increasing GDF-11.

Beatriz Mena-Montes, David Hernández-Álvarez, Gibrán Pedraza-Vázquez, Rafael Toledo-Pérez, Raúl Librado-Osorio, Jorge Antonio García-Álvarez, Adriana Alarcón-Aguilar, Roberto Lazzarini-Lechuga, Oscar Rosas-Carrasco, Mina Königsberg and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. 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

12 authors at 4 institutions in 1 country.

Beatriz Mena-MontesPosgrado en Biología Experimental, DCBS, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0003-3420-0070
David Hernández-ÁlvarezLaboratorio de Bioenergética y Envejecimiento Celular, Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.
Gibrán Pedraza-VázquezPosgrado en Biología Experimental, DCBS, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0002-3339-4515
Rafael Toledo-PérezPosgrado en Biología Experimental, DCBS, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.
Raúl Librado-OsorioDeparmento Investigación Básica, Instituto Nacional de Geriatría, Ciudad de México, Mexico.
Jorge Antonio García-ÁlvarezFacultad de Ciencias, Universidad Nacional Autónoma de México, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0003-2473-7608
Adriana Alarcón-AguilarLaboratorio de Bioenergética y Envejecimiento Celular, Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0002-7669-311X
Roberto Lazzarini-LechugaDepartamento de Biología de la Reproducción, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0003-3537-1576
Oscar Rosas-CarrascoDepartamento de Investigación Clínica-Epidemiológica, Instituto Nacional de Geriatría, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0002-0564-5882
Mina KönigsbergLaboratorio de Bioenergética y Envejecimiento Celular, Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0002-2884-8770
Norma Edith López-DiazguerreroLaboratorio de Bioenergética y Envejecimiento Celular, Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana Iztapalapa, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0001-7470-9360
Armando Luna-LópezDeparmento Investigación Básica, Instituto Nacional de Geriatría, Ciudad de México, Mexico.ORCID https://orcid.org/0000-0001-7941-5695
Universidad Autónoma Metropolitana · MXInstituto Nacional de Pediatria · MXIbero American University · MXUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The loss of skeletal muscle mass and strength is known as sarcopenia; it is characterized as a progressive and generalized muscle disorder associated with aging. This deterioration can seriously compromise the elderly's health and reduce their quality of life. In addition to age, there are other factors that induce muscle mass loss, among which are sedentary lifestyle, chronic diseases, inflammation, and obesity. In recent years, a new clinical condition has been observed in older adults that affects their physical capacities and quality of life, which is known as osteosarcopenic obesity (OSO). Osteoporosis, sarcopenia, and obesity coexist in this condition. Physical exercise and nutritional management are the most widely used interventions for the treatment and prevention of sarcopenia. However, in older adults, physical exercise and protein intake do not have the same outcomes observed in younger people. Here, we used a low-intensity exercise routine for a long period of time (LIERLT) in order to delay the OSO appearance related to sedentarism and aging in female Wistar rats. The LIERLT routine consisted of walking at 15 m/min for 30 min, five days a week for 20 months. To evaluate the effects of the LIERLT routine, body composition was determined using DXA-scan, additionally, biochemical parameters, inflammatory profile, oxidative protein damage, redox state, and serum concentration of GDF-11 at different ages were evaluated (4, 8, 12, 18, 22, and 24 months). Our results show that the LIERLT routine delays OSO phenotype in old 24-month-old rats, in a mechanism involving the decrease in the inflammatory state and oxidative stress. GDF-11 was evaluated as a protein related to muscle repair and regeneration; interestingly, rats that perform the LIERLT increased their GDF-11 levels.

Indexed as

AnimalsFemaleGrowth Differentiation FactorsInflammationOsteoporosisOxidative StressPhysical Conditioning, AnimalRatsRats, WistarSarcopeniaGdf11 protein, ratGrowth Differentiation Factors

Identifiers

PMID34336096
PMCPMC8315843
OpenAlexW3184672095

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.