Evidence map›Paper›PMID 29920215›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2018

Analysis of short-term treatment with the phosphodiesterase type 5 inhibitor tadalafil on long bone development in young rats.

Luqiang Wang, Haoruo Jia, Robert J Tower, Michael A Levine, Ling Qin

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Repurposing erectile dysfunction drugs tadalafil and vardenafil to increase bone mass.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

5 authors at 4 institutions in 2 countries.

Luqiang WangDepartment of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania.
Haoruo JiaDepartment of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania.
Robert J TowerDepartment of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania.
Michael A LevineDepartment of Pediatrics, Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania.ORCID 0000-0003-0036-7809
Ling QinDepartment of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania.
University of Pennsylvania · USChildren's Hospital of Philadelphia · USFirst Affiliated Hospital of Shihezi University Medical College · CNQilu Hospital of Shandong University · CN

Funding

Overall: Resource-based Center for Musculoskeletal Disorders Research (Overall Application)P30AR069619 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LOUIS J SOSLOWSKY · 2016 to 2026
$9.1M
Mechanism of radiotherapy-induced osteoporosis and its treatmentR01AR066098 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI QIN, LING · 2015 to 2019
$1.8M
Role of EGFR signaling in bone formation and the anabolic actions of PTHR01DK095803 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI QIN, LING · 2013 to 2017
$1.7M
NIAMS NIH HHS P30 AR069619NIAMS NIH HHS R01 AR066098NIDDK NIH HHS R01 DK095803
6 · The paper itself

Abstract

Cyclic GMP (cGMP) is an important intracellular regulator of endochondral bone growth and skeletal remodeling. Tadalafil, an inhibitor of the phosphodiesterase (PDE) type 5 (PDE5) that specifically hydrolyzes cGMP, is increasingly used to treat children with pulmonary arterial hypertension (PAH), but the effect of tadalafil on bone growth and strength has not been previously investigated. In this study, we first analyzed the expression of transcripts encoding PDEs in primary cultures of chondrocytes from newborn rat epiphyses. We detected robust expression of PDE5 as the major phosphodiesterase hydrolyzing cGMP. Time-course experiments showed that C-type natriuretic peptide increased intracellular levels of cGMP in primary chondrocytes with a peak at 2 min, and in the presence of tadalafil the peak level of intracellular cGMP was 37% greater ( P < 0.01) and the decline was significantly attenuated. Next, we treated 1-mo-old Sprague Dawley rats with vehicle or tadalafil for 3 wk. Although 10 mg·kg

Indexed as

AnimalsAnimals, NewbornBone and BonesBone DevelopmentCancellous BoneChondrocytesCortical BoneCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5EpiphysesMaleNatriuretic Peptide, C-TypePhosphodiesterase 5 InhibitorsRatsRats, Sprague-DawleyRNA, MessengerCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5Natriuretic Peptide, C-TypePhosphodiesterase 5 InhibitorsRNA, MessengerTadalafilboneendochondral ossificationgrowth platePDE5 inhibitoryoung rat

Identifiers

PMID29920215
PMCPMC6230700
OpenAlexW2809042231

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.