Evidence map›Paper›PMID 25807042›Full record

ArticleEndocrinology2015

Estrogens prevent metabolic dysfunctions induced by circadian disruptions in female mice.

Liangru Zhu, Fang Zou, Yongjie Yang, Pingwen Xu, Kenji Saito, Antentor Othrell Hinton, Xiaofeng Yan, Hongfang Ding, Qi Wu, Makoto Fukuda and 3 more

Abstract read
In one paragraph

Article in Endocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Treating menopause - MHT and beyond.Nature reviews. Endocrinology · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Circadian Clock, Time-Restricted Feeding and Reproduction.International journal of molecular sciences · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 1 institution in 2 countries.

Liangru ZhuChildren's Nutrition Research Center (L.Z., F.Z., Y.Y., P.X., K.S., A.O.H., X.Y., H.D., Q.W., M.F., Y.X.), Department of Pediatrics; Diabetes Research Center (Z.S.), Department of Medicine; and Department of Molecular and Cellular Biology (Z.S., Y.X.), Baylor College of Medicine; and Brown Foundation Institute of Molecular Medicine (Q.T.), University of Texas Health Science Center at Houston, Houston, Texas 77030; and Department of Gastroenterology (L.Z.), Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, People's Republic of China.
Fang Zou
Yongjie Yang
Pingwen Xu
Kenji Saito
Antentor Othrell Hinton
Xiaofeng Yan
Hongfang Ding
Qi Wu
Makoto Fukuda
Zheng Sun
Qingchun Tong
Yong Xu
Children's Nutrition Research Center at Baylor College of Medicine · US

Funding

Initiative for Maximizing Student Development (IMSD) ProgramR25GM056929 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI PEREIRA, FRED A · 1998 to 2023
$12.4M
Diabetes Endocrinology Research CenterP30DK079638 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI CHAN, LAWRENCE · 2008 to 2012
$6.4M
Sim1 Neurons and Body Weight RegulationR01DK092605 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TONG, QINGCHUN · 2012 to 2016
$1.7M
CNS Circuits Mediating Estrogenic Regulation on Energy and Glucose HomeostasisR01DK093587 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI XU, YONG · 2011 to 2015
$1.6M
Targeting hypothalamic steroid receptor co-activator-1 to treat obesityR01DK101379 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI XU, YONG · 2014 to 2017
$1.2M
Epigenomic regulation of metabolism in muscle by circadian clock and environmentR00DK099443 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI SUN, ZHENG · 2014 to 2016
$747k
A Novel AgRP Neurons to the Dorsal Raphe Circuit in Control of Energy ExpenditureR56DK109194 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI WU, QI · 2016 to 2016
$105k
NIDDK NIH HHS P30 DK079638NIDDK NIH HHS R00 DK099443NIDDK NIH HHS R00DK099443NIDDK NIH HHS R01 DK092605NIDDK NIH HHS R01DK092605NIDDK NIH HHS R01 DK093587NIDDK NIH HHS R01DK093587NIDDK NIH HHS R01 DK101379NIDDK NIH HHS R01DK101379NIDDK NIH HHS R56 DK109194NIGMS NIH HHS R25 GM056929
6 · The paper itself

Abstract

Circadian disruption has become a significant factor contributing to the epidemics of obesity and insulin resistance. However, interventions to treat metabolic dysfunctions induced by circadian disruptions are limited. The ovarian hormone, estrogen, produces important antiobesity and antidiabetic effects in female animals and has profound effects on daily behavioral rhythms. Here, we show that in female mice depleted with endogenous estrogens, a jet-lag paradigm induced visceral fat accumulation and systemic insulin resistance, which were associated with altered expression of multiple circadian genes in the visceral fat depot. Interestingly, all these jet-lag-induced deficits were completely rescued in female mice supplemented with exogenous estrogens. We further examined 24-hour oscillations of circadian genes in adipose tissues in female mice with estrogen depletion or replacement and showed that expression levels of the circadian gene, period circadian protein homolog 2, oscillate in visceral adipose tissue in an estrogen-dependent manner. Together, our results indicate that estrogens interact with the intrinsic circadian clock in adipose tissue and prevent abnormal lipid accumulation caused by circadian disruptions.

Indexed as

Adipose TissueAdipose Tissue, WhiteAnimalsCircadian RhythmEstrogensFemaleMiceMice, Inbred C57BLEstrogens

Identifiers

PMID25807042
PMCPMC4430614
OpenAlexW1992794338

What OpenQuestion holds

Textmetadata
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.