Evidence map›Paper›PMID 28090585›Full record

ArticleeNeuro

Circadian Forced Desynchrony of the Master Clock Leads to Phenotypic Manifestation of Depression in Rats.

Miriam Ben-Hamo, Tracy A Larson, Leanne S Duge, Carl Sikkema, Charles W Wilkinson, Horacio O de la Iglesia, Mónica M C González

Abstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Role of chronotype in depression.World journal of psychiatry · 2025
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  15. Neurology international · 2021
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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

7 authors.

Miriam Ben-HamoDepartment of Biology; Program in Neuroscience, University of Washington, Seattle, WA 98195.ORCID 0000-0002-4879-3658
Tracy A LarsonDepartment of Biology.ORCID 0000-0002-4936-7685
Leanne S DugeDepartment of Biology.ORCID 0000-0003-2493-9373
Carl SikkemaGeriatric Research, Education and Clinical Center, VA Puget Sound Health Care System, Seattle, WA 98108; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195.
Charles W WilkinsonGeriatric Research, Education and Clinical Center, VA Puget Sound Health Care System, Seattle, WA 98108; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195.ORCID 0000-0002-5390-0294
Horacio O de la IglesiaDepartment of Biology; Program in Neuroscience, University of Washington, Seattle, WA 98195.ORCID 0000-0003-0855-6807
Mónica M C GonzálezDepartment of Biology.ORCID 0000-0001-5956-1361

Funding

Role of GABA on circadian and homeostatic regulation of sleepR01NS094211 · NINDS · UNIVERSITY OF WASHINGTON · PI DE LA IGLESIA, HORACIO O · 2015 to 2018
$1.4M
Forced Desynchronization of the Rat Circadian SystemR01MH075016 · NIMH · UNIVERSITY OF WASHINGTON · PI DE LA IGLESIA, HORACIO O · 2006 to 2009
$956k
NIMH NIH HHS R01 MH075016NINDS NIH HHS R01 NS094211
6 · The paper itself

Abstract

In mammals, a master circadian clock within the suprachiasmatic nucleus (SCN) of the hypothalamus maintains the phase coherence among a wide array of behavioral and physiological circadian rhythms. Affective disorders are typically associated with disruption of this fine-tuned "internal synchronization," but whether this internal misalignment is part of the physiopathology of mood disorders is not clear. To date, depressive-like behavior in animal models has been induced by methods that fail to specifically target the SCN regulation of internal synchronization as the mode to generate depression. In the rat, exposure to a 22-h light-dark cycle (LD22) leads to the uncoupling of two distinct populations of neuronal oscillators within the SCN. This genetically, neurally, and pharmacologically intact animal model represents a unique opportunity to assess the effect of a systematic challenge to the central circadian pacemaker on phenotypic manifestations of mood disorders. We show that LD22 circadian forced desynchrony in rats induces depressive-like phenotypes including anhedonia, sexual dysfunction, and increased immobility in the forced swim test (FST), as well as changes in the levels and turnover rates of monoamines within the prefrontal cortex. Desynchronized rats show increased FST immobility during the dark (active) phase but decreased immobility during the light (rest) phase, suggesting a decrease in the amplitude of the normal daily oscillation in this behavioral manifestation of depression. Our results support the notion that the prolonged internal misalignment of circadian rhythms induced by environmental challenge to the central circadian pacemaker may constitute part of the etiology of depression.

Indexed as

PhotoperiodAnimalsCircadian ClocksCohort StudiesDepressive DisorderDisease Models, AnimalExploratory BehaviorFood PreferencesMaleMotor ActivityPhenotypeRats, WistarSaccharinSexual Behavior, AnimalSexual Dysfunctions, PsychologicalSwimmingSaccharinbehaviorcircadian rhythmsdepressionemotionrat

Identifiers

PMID28090585
PMCPMC5216685

What OpenQuestion holds

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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.