Evidence map›Paper›PMID 34573029›Full record

ArticleAntioxidants (Basel, Switzerland)2021

Female Mice Reaching Exceptionally High Old Age Have Preserved 20S Proteasome Activities.

Irene Martínez de Toda, Suresh I S Rattan, Mónica De la Fuente, Lorena Arranz

Abstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2021. 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. Review
  2. Longevity, Centenarians and Modified Cellular Proteodynamics.International journal of molecular sciences · 2023
    Review
  3. Article
  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

4 authors.

Irene Martínez de TodaDepartment of Genetics, Physiology and Microbiology (Unit of Animal Physiology), Faculty of Biology, Complutense University, 28040 Madrid, Spain.
Suresh I S RattanDepartment of Molecular Biology and Genetics, Århus University, 8000 Århus, Denmark.ORCID 0000-0002-3478-1381
Mónica De la FuenteDepartment of Genetics, Physiology and Microbiology (Unit of Animal Physiology), Faculty of Biology, Complutense University, 28040 Madrid, Spain.
Lorena ArranzDepartment of Genetics, Physiology and Microbiology (Unit of Animal Physiology), Faculty of Biology, Complutense University, 28040 Madrid, Spain.ORCID 0000-0002-5896-4238

Funding

ISCIII-FEDER PI15/01787Ministerio de Ciencia e Innovación FPU and mobility grantsNorthern Norway Regional Health Authority HNF1338-17Northern Norway Regional Health Authority and UiT 2014/5668Norwegian Cancer Society 6765150Research Council of Norway Stem Cell Program, 247596; FRIPRO Program, 250901UCM UCM-Research Group
6 · The paper itself

Abstract

Oxidized, damaged and misfolded proteins accumulate during aging and contribute to impaired cell function and tissue homeodynamics. Damaged proteins are degraded by cellular clearance mechanisms like the 20S proteasome. Aging relates to low 20S proteasome function, whereas long-lived species show high levels. However, contradictory results exist depending on the tissue or cell type and it is unknown how the 20S proteasome functions in exceptionally old mice. The aim of this study was to investigate two proteasome activities (caspase-like and chymotrypsin-like) in several tissues (lung, heart, axillary lymph nodes, liver, kidney) and cells (peritoneal leukocytes) from adult (28 ± 4 weeks,

Indexed as

20S proteasomeagingcaspase-like activitychymotrypsin-like activityexceptionally oldhealthy aging

Identifiers

PMID34573029
PMCPMC8472714

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.