Evidence map›Paper›PMID 31953150›Full record

ArticleFree radical biology & medicine2020

Deletion of Nrf2 shortens lifespan in C57BL6/J male mice but does not alter the health and survival benefits of caloric restriction.

Laura C D Pomatto, Theresa Dill, Bethany Carboneau, Sophia Levan, Jonathan Kato, Evi M Mercken, Kevin J Pearson, Michel Bernier, Rafael de Cabo

Open access · greenAbstract read
In one paragraph

Article in Free radical biology & medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  18. Aged Nrf2-Null Mice Develop All Major Types of Age-Related Cataracts.Investigative ophthalmology & visual science · 2021
    Article
  19. Review
  20. HepaticNutrients · 2021
    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

9 authors at 1 institution in 1 country.

Laura C D PomattoTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA; National Institute on General Medical Sciences, National Institute of Health, Bethesda, MD, 20892, USA.
Theresa DillTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA.
Bethany CarboneauTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA.
Sophia LevanTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA.
Jonathan KatoTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA.
Evi M MerckenTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA.
Kevin J PearsonTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA.
Michel BernierTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA.
Rafael de CaboTranslational Gerontology Branch, National Institute on Aging, National Institute of Health, Baltimore, MD, 21224, USA. Electronic address: decaboRa@mail.nih.gov.
National Institute on Aging · US

Funding

NRF2 interactions with SIRT1 and its role on caloric restrictionZIAAG000361 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2009 to 2024
$5.3M
Calorie restriction and agingZ01AG000368 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2005 to 2008
$1.4M
Aging and CR effects on the Plasma Membrane Redox SystemZ01AG000362 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2008 to 2008
$422k
A multi-system approach to ameliorate the age-dependent loss of the Nrf2-mediated cellular stress response: implications on stress adaptation and longevity.FI2GM123963 · NIGMS · U.S. NATIONAL INSTITUTE ON AGING · PI CORRALES-DIAZ POMATTO, LAURA · 2017 to 2017
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Intramural NIH HHS Z01 AG000362Intramural NIH HHS Z01 AG000368Intramural NIH HHS ZIA AG000361NIGMS NIH HHS FI2 GM123963
6 · The paper itself

Abstract

Caloric restriction (CR) is the leading non-pharmaceutical dietary intervention to improve health- and lifespan in most model organisms. A wide array of cellular pathways is induced in response to CR and CR-mimetics, including the transcriptional activator Nuclear factor erythroid-2-related factor 2 (Nrf2), which is essential in the upregulation of multiple stress-responsive and mitochondrial enzymes. Nrf2 is necessary in tumor protection but is not essential for the lifespan extending properties of CR in outbred mice. Here, we sought to study Nrf2-knockout (KO) mice and littermate controls in male C57BL6/J, an inbred mouse strain. Deletion of Nrf2 resulted in shortened lifespan compared to littermate controls only under ad libitum conditions. CR-mediated lifespan extension and physical performance improvements did not require Nrf2. Metabolic and protein homeostasis and activation of tissue-specific cytoprotective proteins were dependent on Nrf2 expression. These results highlight an important contribution of Nrf2 for normal lifespan and stress response.

Indexed as

Caloric RestrictionLongevityAnimalsMaleMiceMice, Inbred C57BLMice, KnockoutNF-E2-Related Factor 2NF-E2-Related Factor 2

Identifiers

PMID31953150
PMCPMC7382945
OpenAlexW2999130535

What OpenQuestion holds

Textmetadata
LicenceTDM
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.