Evidence map›Paper›PMID 23594144›Full record

ReviewCritical reviews in biochemistry and molecular biology

Metabolism as an integral cog in the mammalian circadian clockwork.

Karen L Gamble, Martin E Young

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in biochemistry and molecular biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Physiological processes underlying organ injury in alcohol abuse.American journal of physiology. Endocrinology and metabolism · 2016
    Review
  8. Article
  9. Review
  10. Article
  11. REV-ERB and ROR nuclear receptors as drug targets.Nature reviews. Drug discovery · 2014
    Review
  12. Article
  13. 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

2 authors at 1 institution in 1 country.

Karen L GambleDivision of Behavioral Neurobiology, Department of Psychiatry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Martin E Young
University of Alabama at Birmingham · US

Funding

UAB Center for Clinical and Translational Science (CCTS) UL1UL1TR000165 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2012 to 2013
$9.6M
Circadian dysfunction and neurodegenerative diseaseR01NS082413 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GAMBLE, KAREN L · 2013 to 2022
$4.6M
Role of the Molecular Circadian Clock within the HeartR01HL074259 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI YOUNG, MARTIN E · 2004 to 2012
$3.1M
Integration of photic and nonphotic signaling in the circadian pacemakerR00GM086683 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GAMBLE, KAREN L · 2009 to 2011
$740k
Time-of-Day-Dependent Feeding Influences Myocardial FunctionR21HL106199 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YOUNG, MARTIN E · 2011 to 2012
$403k
Influence of the Cardiomyocyte Circadian Clock on Cardiac HypertrophyR21HL107709 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YOUNG, MARTIN E · 2012 to 2013
$392k
Integration of photic and nonphotic signaling in the circadian pacemakerK99GM086683 · NIGMS · VANDERBILT UNIVERSITY · PI GAMBLE, KAREN L · 2009 to 2009
$70k
NCATS NIH HHS UL1 TR-000165NCATS NIH HHS UL1 TR000165NHLBI NIH HHS HL-074259NHLBI NIH HHS HL-106199NHLBI NIH HHS HL-107709NHLBI NIH HHS R01 HL074259NHLBI NIH HHS R21 HL106199NHLBI NIH HHS R21 HL107709NIGMS NIH HHS GM-086683NIGMS NIH HHS K99 GM086683NIGMS NIH HHS R00 GM086683NINDS NIH HHS NS-082413NINDS NIH HHS R01 NS082413
6 · The paper itself

Abstract

Circadian rhythms are an integral part of life. These rhythms are apparent in virtually all biological processes studies to date, ranging from the individual cell (e.g. DNA synthesis) to the whole organism (e.g. behaviors such as physical activity). Oscillations in metabolism have been characterized extensively in various organisms, including mammals. These metabolic rhythms often parallel behaviors such as sleep/wake and fasting/feeding cycles that occur on a daily basis. What has become increasingly clear over the past several decades is that many metabolic oscillations are driven by cell-autonomous circadian clocks, which orchestrate metabolic processes in a temporally appropriate manner. During the process of identifying the mechanisms by which clocks influence metabolism, molecular-based studies have revealed that metabolism should be considered an integral circadian clock component. The implications of such an interrelationship include the establishment of a vicious cycle during cardiometabolic disease states, wherein metabolism-induced perturbations in the circadian clock exacerbate metabolic dysfunction. The purpose of this review is therefore to highlight recent insights gained regarding links between cell-autonomous circadian clocks and metabolism and the implications of clock dysfunction in the pathogenesis of cardiometabolic diseases.

Indexed as

AnimalsCircadian RhythmEnergy MetabolismHomeostasisHumansMammals

Identifiers

PMID23594144
PMCPMC3862897
OpenAlexW2007270297

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.