Evidence map›Paper›PMID 32841230›Full record

ArticlePLoS genetics2020

Gluconeogenesis and PEPCK are critical components of healthy aging and dietary restriction life extension.

Brian Onken, Natallia Kalinava, Monica Driscoll

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  12. Age-Related Increase in Lactate Dehydrogenase Activity in Skeletal Muscle Reduces Life Span in Drosophila.The journals of gerontology. Series A, Biological sciences and medical sciences · 2022
    Article
  13. Review
  14. 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

3 authors at 1 institution in 1 country.

Brian OnkenDepartment of Molecular Biology and Biochemistry Rutgers University, Piscataway, NJ, United States of America.ORCID 0000-0001-8818-4497
Natallia KalinavaDepartment of Molecular Biology and Biochemistry Rutgers University, Piscataway, NJ, United States of America.ORCID 0000-0002-3346-8051
Monica DriscollDepartment of Molecular Biology and Biochemistry Rutgers University, Piscataway, NJ, United States of America.ORCID 0000-0002-8751-7429
Rutgers, The State University of New Jersey · US

Funding

Genetic Dissection of Mechanisms by Which Exercise Promotes Systemic HealthR01AG051995 · NIA · RUTGERS, THE STATE UNIV OF N.J. · PI DRISCOLL, MONICA A. · 2016 to 2020
$2.0M
Mechanisms modulating the maintenance of structural integrity in individual agingR01AG046358 · NIA · RUTGERS, THE STATE UNIV OF N.J. · PI DRISCOLL, MONICA A. · 2013 to 2017
$1.5M
NIA NIH HHS R01 AG046358NIA NIH HHS R01 AG051995
6 · The paper itself

Abstract

High glucose diets are unhealthy, although the mechanisms by which elevated glucose is harmful to whole animal physiology are not well understood. In Caenorhabditis elegans, high glucose shortens lifespan, while chemically inflicted glucose restriction promotes longevity. We investigated the impact of glucose metabolism on aging quality (maintained locomotory capacity and median lifespan) and found that, in addition to shortening lifespan, excess glucose negatively impacts locomotory healthspan. Conversely, disrupting glucose utilization by knockdown of glycolysis-specific genes results in large mid-age physical improvements via a mechanism that requires the FOXO transcription factor DAF-16. Adult locomotory capacity is extended by glycolysis disruption, but maximum lifespan is not, indicating that limiting glycolysis can increase the proportion of life spent in mobility health. We also considered the largely ignored role of glucose biosynthesis (gluconeogenesis) in adult health. Directed perturbations of gluconeogenic genes that specify single direction enzymatic reactions for glucose synthesis decrease locomotory healthspan, suggesting that gluconeogenesis is needed for healthy aging. Consistent with this idea, overexpression of the central gluconeogenic gene pck-2 (encoding PEPCK) increases health measures via a mechanism that requires DAF-16 to promote pck-2 expression in specific intestinal cells. Dietary restriction also features DAF-16-dependent pck-2 expression in the intestine, and the healthspan benefits conferred by dietary restriction require pck-2. Together, our results describe a new paradigm in which nutritional signals engage gluconeogenesis to influence aging quality via DAF-16. These data underscore the idea that promotion of gluconeogenesis might be an unappreciated goal for healthy aging and could constitute a novel target for pharmacological interventions that counter high glucose consequences, including diabetes.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCaloric RestrictionForkhead Transcription FactorsGene Expression Regulation, DevelopmentalGluconeogenesisGlucoseHealthy AgingHumansLife ExpectancyLongevityPhosphoenolpyruvate Carboxykinase (ATP)Signal TransductionCaenorhabditis elegans Proteinsdaf-16 protein, C elegansForkhead Transcription FactorsGlucosePCK2 protein, humanPhosphoenolpyruvate Carboxykinase (ATP)

Identifiers

PMID32841230
PMCPMC7473531
OpenAlexW3081141051

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.