Evidence map›Paper›PMID 25502949›Full record

ArticlePloS one2014

Circadian mechanisms of food anticipatory rhythms in rats fed once or twice daily: clock gene and endocrine correlates.

Danica F Patton, Angela M Katsuyama, Ilya Pavlovski, Mateusz Michalik, Zachary Patterson, Maksim Parfyonov, Andrea N Smit, Elliott G Marchant, Seung Hwan Chung, John Chung and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

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  10. Flexible clock systems: adjusting the temporal programme.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Danica F PattonDepartment of Psychology, Simon Fraser University, Burnaby, BC, Canada.
Angela M KatsuyamaDepartment of Biology, University of Washington, Seattle, WA, United States of America.
Ilya PavlovskiDepartment of Psychology, Simon Fraser University, Burnaby, BC, Canada.
Mateusz MichalikDepartment of Psychology, Simon Fraser University, Burnaby, BC, Canada.
Zachary PattersonDepartment of Neuroscience, Carleton University, Ottawa, ON, Canada.
Maksim ParfyonovDepartment of Psychology, Simon Fraser University, Burnaby, BC, Canada.
Andrea N SmitDepartment of Psychology, Simon Fraser University, Burnaby, BC, Canada.
Elliott G MarchantDepartment of Psychology, Simon Fraser University, Burnaby, BC, Canada.
Seung Hwan Chung
John ChungDepartment of Biology, University of Washington, Seattle, WA, United States of America.
Alfonso AbizaidDepartment of Neuroscience, Carleton University, Ottawa, ON, Canada.
Kai-Florian StorchDepartment of Psychiatry, McGill University, Montreal, PQ, Canada.
Horacio de la IglesiaDepartment of Biology, University of Washington, Seattle, WA, United States of America.
Ralph E MistlbergerDepartment of Psychology, Simon Fraser University, Burnaby, BC, Canada.
Simon Fraser University · CAUniversity of Washington · USCarleton University · CAMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circadian clocks in many brain regions and peripheral tissues are entrained by the daily rhythm of food intake. Clocks in one or more of these locations generate a daily rhythm of locomotor activity that anticipates a regular mealtime. Rats and mice can also anticipate two daily meals. Whether this involves 1 or 2 circadian clocks is unknown. To gain insight into how the circadian system adjusts to 2 daily mealtimes, male rats in a 12∶12 light-dark cycle were fed a 2 h meal either 4 h after lights-on or 4 h after lights-off, or a 1 h meal at both times. After 30 days, brain, blood, adrenal and stomach tissue were collected at 6 time points. Multiple clock genes from adrenals and stomachs were assayed by RT-PCR. Blood was assayed for corticosterone and ghrelin. Bmal1 expression was quantified in 14 brain regions by in situ hybridization. Clock gene rhythms in adrenal and stomach from day-fed rats oscillated in antiphase with the rhythms in night-fed rats, and at an intermediate phase in rats fed twice daily. Corticosterone and ghrelin in 1-meal rats peaked at or prior to the expected mealtime. In 2-meal rats, corticosterone peaked only prior the nighttime meal, while ghrelin peaked prior to the daytime meal and then remained elevated. The olfactory bulb, nucleus accumbens, dorsal striatum, cerebellum and arcuate nucleus exhibited significant daily rhythms of Bmal1 in the night-fed groups that were approximately in antiphase in the day-fed groups, and at intermediate levels (arrhythmic) in rats anticipating 2 daily meals. The dissociations between anticipatory activity and the peripheral clocks and hormones in rats anticipating 2 daily meals argue against a role for these signals in the timing of behavioral rhythms. The absence of rhythmicity at the tissue level in brain regions from rats anticipating 2 daily meals support behavioral evidence that circadian clock cells in these tissues may reorganize into two populations coupled to different meals.

Indexed as

Anticipation, PsychologicalFoodAdrenal GlandsAnimalsARNTL Transcription FactorsBrainCircadian ClocksCorticosteroneGastric MucosaGhrelinHormonesMaleMiceMotor ActivityPeriod Circadian ProteinsRatsARNTL Transcription FactorsCorticosteroneGhrelinHormonesPer1 protein, ratPer2 protein, ratPeriod Circadian Proteins

Identifiers

PMID25502949
PMCPMC4263600
OpenAlexW2022850582

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.