Evidence map›Paper›PMID 25926681›Full record

ReviewJournal of biological rhythms2015

Adipose Clocks: Burning the Midnight Oil.

Emma Henriksson, Katja A Lamia

Abstract readReview
In one paragraph

Review in Journal of biological rhythms, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 21% 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

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

  1. Pooled it
  2. SerumFrontiers in nutrition · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Clocking In, Working Out: Circadian Regulation of Exercise Physiology.Trends in endocrinology and metabolism: TEM · 2019
    Review
  7. Article
  8. 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 2 countries.

Emma HenrikssonDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, California, USA Department of Clinical Sciences, Lund University, CRC, Malmö, Sweden.
Katja A LamiaDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, California, USA klamia@scripps.edu.
Scripps Research Institute · US

Funding

Circadian molecular regulation of the xenobiotic responseR01DK097164 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LAMIA, KATJA A · 2013 to 2017
$2.1M
Circadian Repressors Cry1 and Cry2 Modulate Nuclear Hormone Receptor FunctionK01DK090188 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LAMIA, KATJA A · 2011 to 2013
$446k
NIDDK NIH HHS K01 DK090188NIDDK NIH HHS R01 DK097164
6 · The paper itself

Abstract

Circadian clocks optimize the timing of physiological processes in synchrony with daily recurring and therefore predictable changes in the environment. Until the late 1990s, circadian clocks were thought to exist only in the central nervous systems of animals; elegant studies in cultured fibroblasts and using genetically encoded reporters in Drosophila melanogaster and in mice showed that clocks are ubiquitous and cell autonomous. These findings inspired investigations of the advantages construed by enabling each organ to independently adjust its function to the time of day. Studies of rhythmic gene expression in several organs suggested that peripheral organ clocks might play an important role in optimizing metabolic physiology by synchronizing tissue-intrinsic metabolic processes to cycles of nutrient availability and energy requirements. The effects of clock disruption in liver, pancreas, muscle, and adipose tissues support that hypothesis. Adipose tissues coordinate energy storage and utilization and modulate behavior and the physiology of other organs by secreting hormones known as "adipokines." Due to behavior- and environment-driven diurnal variations in supply and demand for chemical and thermal energy, adipose tissues might represent an important peripheral location for coordinating circadian energy balance (intake, storage, and utilization) over the whole organism. Given the complexity of adipose cell types and depots, the sensitivity of adipose tissue biology to age and diet composition, and the plethora of known and yet-to-be-discovered adipokines and lipokines, we have just begun to scratch the surface of understanding the role of circadian clocks in adipose tissues.

Indexed as

AdipocytesAdipose TissueAnimalsCircadian ClocksCircadian RhythmCircadian Rhythm Signaling Peptides and ProteinsFatsHumansLipid MetabolismModels, BiologicalCircadian Rhythm Signaling Peptides and ProteinsFatsadipocyteadiposecircadianclockPPARγReverbα

Identifiers

PMID25926681
PMCPMC4567910
OpenAlexW2071616287

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.