Evidence map›Paper›PMID 36620217›Full record

ArticleFrontiers in physiology2022

Acute hypoxia induced dysregulation of clock-controlled ovary functions.

Mengnan Ding, Yarong Lu, Xin Huang, Chen Xing, Shaojun Hou, Dongxue Wang, Yifan Zhang, Wei Wang, Chongchong Zhang, Min Zhang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2022. 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
1.1field-weighted citation impact, top 26% 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, 12 citations in OpenAlex.

  1. Article
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  5. Observational
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  8. Review
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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

15 authors at 5 institutions in 1 country.

Mengnan DingBeijing Institute of Basic Medical Sciences, Beijing, China.
Yarong LuBeijing Institute of Basic Medical Sciences, Beijing, China.
Xin HuangBeijing Institute of Basic Medical Sciences, Beijing, China.
Chen XingBeijing Institute of Basic Medical Sciences, Beijing, China.
Shaojun HouBeijing Institute of Basic Medical Sciences, Beijing, China.
Dongxue WangBeijing Institute of Basic Medical Sciences, Beijing, China.
Yifan ZhangBeijing Institute of Basic Medical Sciences, Beijing, China.
Wei WangBeijing Institute of Basic Medical Sciences, Beijing, China.
Chongchong ZhangBeijing Institute of Basic Medical Sciences, Beijing, China.
Min ZhangBeijing Institute of Basic Medical Sciences, Beijing, China.
Fanfei MengBeijing Institute of Basic Medical Sciences, Beijing, China.
Kun LiuBeijing Institute of Basic Medical Sciences, Beijing, China.
Guangchao LiuHenan University Joint National Laboratory for Antibody Drug Engineering, Kaifeng, China.
Jincheng ZhaoSchool of Pharmacy, Jiamus University, Jiamusi, China.
Lun SongBeijing Institute of Basic Medical Sciences, Beijing, China.
Beijing Institute of Education · CNInstitute of Basic Medical Sciences of the Chinese Academy of Medical SciencesJiamusi University · CNAnhui Medical University · CNHenan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High altitudes or exposure to hypoxia leads to female reproductive disorders. Circadian clocks are intrinsic time-tracking systems that enable organisms to adapt to the Earth's 24-h light/dark cycle, which can be entrained by other environmental stimuli to regulate physiological and pathological responses. In this study, we focused on whether ovarian circadian clock proteins were involved in regulating female reproductive dysfunction under hypoxic conditions. Hypobaric hypoxia was found to induce a significantly prolonged estrous cycle in female mice, accompanied by follicular atresia, pituitary/ovarian hormone synthesis disorder, and decreased LHCGR expression in the ovaries. Under the same conditions, the levels of the ovarian circadian clock proteins, CLOCK and BMAL1, were suppressed, whereas E4BP4 levels were upregulated. Results from granulosa cells (GCs) further demonstrated that CLOCK: BMAL1 and E4BP4 function as transcriptional activators and repressors of LHCGR in ovarian GCs, respectively, whose responses were mediated by HIF1ɑ-dependent (E4BP4 upregulation) and ɑ-independent (CLOCK and BMAL1 downregulation) manners. The LHCGR agonist was shown to efficiently recover the impairment of ovulation-related gene (

Indexed as

circadian clockhigh altitudehypobaric hypoxiaovulationreproductive disorder

Identifiers

PMID36620217
PMCPMC9816144
OpenAlexW4312173931

What OpenQuestion holds

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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.