Evidence map›Paper›PMID 33572215›Full record

ArticleInternational journal of molecular sciences2021

Voluntary Wheel Running Partially Compensates for the Effects of Global Estrogen Receptor-α Knockout on Cortical Bone in Young Male Mice.

Rebecca K Dirkes, Nathan C Winn, Thomas J Jurrissen, Dennis B Lubahn, Victoria J Vieira-Potter, Jaume Padilla, Pamela S Hinton

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Extract ofCells · 2024
    Article
  4. Osterix-driven LINC complex disruption in vivo diminishes osteogenesis at 8 weeks but not at 15 weeks.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2024
    Article
  5. Article
  6. Article
  7. Osterix-driven LINC complex disruptionbioRxiv : the preprint server for biology · 2023
    Article
  8. The Role of Estrogen Receptors in Health and Disease.International journal of molecular sciences · 2023
    Article
  9. Review
  10. Similarities Between Disuse and Age-Induced Bone Loss.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. 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

7 authors at 2 institutions in 1 country.

Rebecca K DirkesNutrition and Exercise Physiology, University of Missouri, Columbia, MO 65211, USA.
Nathan C WinnNutrition and Exercise Physiology, University of Missouri, Columbia, MO 65211, USA.
Thomas J JurrissenNutrition and Exercise Physiology, University of Missouri, Columbia, MO 65211, USA.
Dennis B LubahnDepartment of Biochemistry, University of Missouri, Columbia, MO 65211, USA.
Victoria J Vieira-PotterNutrition and Exercise Physiology, University of Missouri, Columbia, MO 65211, USA.
Jaume PadillaNutrition and Exercise Physiology, University of Missouri, Columbia, MO 65211, USA.
Pamela S HintonNutrition and Exercise Physiology, University of Missouri, Columbia, MO 65211, USA.
University of Missouri · USUniversity of Missouri Health System · US

Funding

American Egg Board 00050021NIH HHS K01 HL-125503
6 · The paper itself

Abstract

Estrogen receptor-α knockout (ERKO) in female, but not male, mice results in an impaired osteogenic response to exercise, but the mechanisms behind this ability in males are unknown. We explored the main and interactive effects of ERKO and exercise on cortical geometry, trabecular microarchitecture, biomechanical strength, and sclerostin expression in male mice. At 12 weeks of age, male C57BL/6J ERKO and WT animals were randomized into two groups: exercise treatment (EX) and sedentary (SED) controls, until 22 weeks of age. Cortical geometry and trabecular microarchitecture were measured via μCT; biomechanical strength was assessed via three-point bending; sclerostin expression was measured via immunohistochemistry. Two-way ANOVA was used to assess sclerostin expression and trabecular microarchitecture; two-way ANCOVA with body weight was used to assess cortical geometry and biomechanical strength. ERKO positively impacted trabecular microarchitecture, and exercise had little effect on these outcomes. ERKO significantly impaired cortical geometry, but exercise was able to partially reverse these negative alterations. EX increased cortical thickness regardless of genotype. There were no effects of genotype or exercise on sclerostin expression. In conclusion, male ERKO mice retain the ability to build bone in response to exercise, but altering sclerostin expression is not one of the mechanisms involved.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBone RemodelingCortical BoneEstrogen Receptor alphaMaleMiceMice, KnockoutModels, AnimalOsteogenesisPhysical Conditioning, AnimalRunningX-Ray MicrotomographyAdaptor Proteins, Signal TransducingEsr1 protein, mouseEstrogen Receptor alphaSost protein, mousebone healthestrogenestrogen receptorsexercisesclerostin

Identifiers

PMID33572215
PMCPMC7915374
OpenAlexW3128416292

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.