Evidence map›Paper›PMID 25806044›Full record

ArticleFrontiers in genetics2015

Aging alters circadian regulation of redox in Drosophila.

Vladimir I Klichko, Eileen S Chow, Joanna Kotwica-Rolinska, William C Orr, Jadwiga M Giebultowicz, Svetlana N Radyuk

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  7. Review
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  9. Aging and the clock: Perspective from flies to humans.The European journal of neuroscience · 2020
    Review
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  11. Article
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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

6 authors at 2 institutions in 1 country.

Vladimir I KlichkoDepartment of Biological Sciences, Southern Methodist University, Dallas TX, USA.
Eileen S ChowDepartment of Integrative Biology, Oregon State University, Corvallis OR, USA.
Joanna Kotwica-RolinskaDepartment of Integrative Biology, Oregon State University, Corvallis OR, USA.
William C OrrDepartment of Biological Sciences, Southern Methodist University, Dallas TX, USA.
Jadwiga M GiebultowiczDepartment of Integrative Biology, Oregon State University, Corvallis OR, USA.
Svetlana N RadyukDepartment of Biological Sciences, Southern Methodist University, Dallas TX, USA.
Oregon State University · USSouthern Methodist University · US

Funding

Circadian Clocks and AgingR01AG045830 · NIA · OREGON STATE UNIVERSITY · PI GIEBULTOWICZ, JADWIGA M, KRETZSCHMAR, DORIS · 2013 to 2017
$1.3M
NIA NIH HHS R01 AG045830
6 · The paper itself

Abstract

Circadian coordination of metabolism, physiology, and neural functions contributes to healthy aging and disease prevention. Clock genes govern the daily rhythmic expression of target genes whose activities underlie such broad physiological parameters as maintenance of redox homeostasis. Previously, we reported that glutathione (GSH) biosynthesis is controlled by the circadian system via effects of the clock genes on expression of the catalytic (Gclc) and modulatory (Gclm) subunits comprising the glutamate cysteine ligase (GCL) holoenzyme. The objective of this study was to determine whether and how aging, which leads to weakened circadian oscillations, affects the daily profiles of redox-active biomolecules. We found that fly aging is associated with altered profiles of Gclc and Gclm expression at both the mRNA and protein levels. Analysis of free aminothiols and GCL activity revealed that aging abolishes daily oscillations in GSH levels and alters the activity of glutathione biosynthetic pathways. Unlike GSH, its precursors and products of catabolism, methionine, cysteine and cysteinyl-glycine, were not rhythmic in young or old flies, while rhythms of the glutathione oxidation product, GSSG, were detectable. We conclude that the temporal regulation of GSH biosynthesis is altered in the aging organism and that age-related loss of circadian modulation of pathways involved in glutathione production is likely to impair temporal redox homeostasis.

Indexed as

agingcircadian clocksDrosophilaglutathioneredox

Identifiers

PMID25806044
PMCPMC4353305
OpenAlexW2055792236

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.