Evidence map›Paper›PMID 31377938›Full record

ArticleJournal of medical ultrasonics (2001)2019

Inhibition of myostatin signal pathway may be involved in low-intensity pulsed ultrasound promoting bone healing.

Lijun Sun, Shuxin Sun, Xinjuan Zhao, Jing Zhang, Jianzhong Guo, Liang Tang, Dean Ta

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of medical ultrasonics (2001), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Bone-muscle crosstalk under physiological and pathological conditions.Cellular and molecular life sciences : CMLS · 2024
    Review
  2. Review
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  5. Article
  6. Review
  7. Article
  8. Bone and Muscle Crosstalk in Aging.Frontiers in cell and developmental biology · 2020
    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

7 authors at 2 institutions in 1 country.

Lijun SunInstitute of Sports Biology, Shaanxi Normal University, Xi'an, 710119, China.
Shuxin SunDepartment of Electronic Engineering, Fudan University, Shanghai, 200433, China.
Xinjuan ZhaoInstitute of Sports Biology, Shaanxi Normal University, Xi'an, 710119, China.
Jing ZhangInstitute of Sports Biology, Shaanxi Normal University, Xi'an, 710119, China.
Jianzhong GuoShaanxi Key Laboratory of Ultrasonics, Shaanxi Normal University, Xi'an, 710119, China.
Liang TangInstitute of Sports Biology, Shaanxi Normal University, Xi'an, 710119, China. tl531@snnu.edu.cn.
Dean TaDepartment of Electronic Engineering, Fudan University, Shanghai, 200433, China. tda@fudan.edu.cn.
Shaanxi Normal University · CNFudan University · CN

Funding

Fundamental Research Funds for the Central Universities GK201703091Fundamental Research Funds for the Central Universities GK201703092National Natural Science Foundation of China 11502134National Natural Science Foundation of China 11727813National Natural Science Foundation of China 11774213National Natural Science Foundation of China 11827808Natural Science Foundation of Shaanxi Province 2018JM1022
6 · The paper itself

Abstract

purposeLow-intensity pulsed ultrasound (LIPUS) is effective in promoting bone healing, and a myostatin deficiency also has a positive effect on bone formation. In this study, we evaluated the effects of LIPUS on bone healing in rats in vivo and investigated the mechanisms in vitro, aiming to explore whether LIPUS promotes bone healing through inhibition of the myostatin signaling pathway.

methodsRats with both drill-hole defects and MC3T3-E1 cells were randomly assigned to a LIPUS group and a control group. The LIPUS group received LIPUS treatment (1.5 MHz, 30 mW/cm

resultsAfter 21 days, the myostatin expression in quadriceps was significantly inhibited in the LIPUS group, and remodeling of the newly formed bone in the drill-hole site was significantly better in the LIPUS group than that in the control group, which was confirmed by micro-CT analysis. After 3 days, LIPUS significantly promoted osteoblast proliferation; inhibited the expression of AcvrIIB (the myostatin receptor), Smad3, p-Smad3, and GSK-3β; and increased Wnt1 and β-catenin expression. Moreover, translocation of β-catenin from the cytolemma to the nucleus was observed in the LIPUS group. However, these effects were blocked by treatment with myostatin recombinant protein.

conclusionsThe results indicate that LIPUS may promote bone healing through inhibition of the myostatin signal pathway.

Indexed as

AnimalsBlotting, WesternCell Culture TechniquesDisease Models, AnimalFemaleFracture HealingFractures, BoneMyostatinPolymerase Chain ReactionRatsRats, Sprague-DawleySignal TransductionTomography, X-Ray ComputedUltrasonic TherapyUltrasonic WavesMyostatinBone healingBone micro-architecturesLow-intensity pulsed ultrasoundMyostatinProliferationWnt

Identifiers

PMID31377938
OpenAlexW2992713766

What Socratic 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 Socratic graph.