Evidence map›Paper›PMID 28974783›Full record

ArticleScientific reports2017

Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice.

Peng Zhang, Guang Li, Hui Li, XiaoQiu Tan, Hai-Ying Mary Cheng

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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  8. Neurology international · 2021
    Article
  9. Review
  10. Contribution of DNA methylation in chronic stress-induced cardiac remodeling and arrhythmias in mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  11. Review
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

5 authors at 4 institutions in 3 countries.

Peng ZhangKey Laboratory of Medical Electrophysiology, Ministry of Education, Institute of Cardiovascular Medicine; Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Disease of Sichuan Province; Southwest Medical University, Luzhou, 646009, China. zhangpeng1440@163.com.
Guang LiKey Laboratory of Medical Electrophysiology, Ministry of Education, Institute of Cardiovascular Medicine; Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Disease of Sichuan Province; Southwest Medical University, Luzhou, 646009, China.
Hui LiKey Laboratory of Medical Electrophysiology, Ministry of Education, Institute of Cardiovascular Medicine; Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Disease of Sichuan Province; Southwest Medical University, Luzhou, 646009, China.
XiaoQiu TanKey Laboratory of Medical Electrophysiology, Ministry of Education, Institute of Cardiovascular Medicine; Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Disease of Sichuan Province; Southwest Medical University, Luzhou, 646009, China.
Hai-Ying Mary ChengDepartment of Biology, University of Toronto Mississauga, 3359 Mississauga Road, Mississauga, ON L5L 1C6, Canada.
Sichuan Center for Disease Control and Prevention · CNMinistry of Education · ROSouthwest Medical University · CNUniversity of Toronto · CA

Funding

CIHR
6 · The paper itself

Abstract

It remains unknown whether chronic circadian disturbance (CCD) during pregnancy can lead to mood disorders in the offspring. Here we show that pregnant mice in the F0 generation that were exposed to CCD stress displayed depression-like behaviors, and produced offspring in the F1 and F2 generations that also exhibited mood-associated behavioral phenotypes despite the lack of direct stressful experiences during their postnatal or adult period. Prenatal CCD stress was correlated with the elevation of plasma corticosterone levels in F1 mice. Furthermore, the diurnal expression profiles of core circadian clock genes were disrupted in the suprachiasmatic nucleus of F1 mice. Proteomics analysis revealed that prenatal CCD stress resulted in distinct changes in protein expression in the hypothalamus of female F1 mice, in particular proteins that were associated with cellular activities, metabolism, development and diseases. Sex-specific differences in melanocortin 4 receptor expression were apparent in the CCD F1 generation. We conclude that maternal exposure to chronic circadian disturbance during pregnancy can lead to sex-specific mood disorders that persist for at least two filial generations. The underlying mechanisms may depend on transgenerational changes in plasma corticosterone levels, circadian pacemaking, and hypothalamic protein expression.

Indexed as

Maternal ExposureAnimalsBehavior, AnimalChronobiology DisordersCircadian ClocksCorticosteroneFemaleGene Expression RegulationHumansHypothalamo-Hypophyseal SystemMiceMood DisordersPituitary-Adrenal SystemPregnancyPrenatal Exposure Delayed EffectsProteomicsCorticosteroneMC4R protein, mouseReceptor, Melanocortin, Type 4

Identifiers

PMID28974783
PMCPMC5626699
OpenAlexW2760360930

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.