Literature DB >> 17920491

Bone formation and tooth movement are synergistically enhanced by administration of EP4 agonist.

Chooryung J Chung1, Hyoung-Seon Baik, Kunimichi Soma.   

Abstract

INTRODUCTION: Stimulation of the prostaglandin receptor EP4 induces bone anabolic responses to external loading. The aim of this study was to determine the possibility of synergistic enhancement of tooth movement along with bone formation in vivo through the stimulation of the prostaglandin receptor EP4.
METHODS: The sample consisted of 25 male rats, 6 to 7 weeks old. Experimental tooth movement was induced in the maxillary right molars with a split-mouth design. During the 7-day experimental period, some rats were injected periodically with a specific EP4 agonist (ONO-AE1-329), a drug that binds to the EP4 receptor to mimic the actions of ligand binding; the injection site was on the tension side in the interproximal region between the first and second molars. Other rats received vehicle injection (saline solution only). For control, EP4 agonist or vehicle was injected into some rats, but tooth movement was not initiated. The amounts of tooth movement and bone volume of the paradental region were evaluated by using soft x-ray and micro-computed tomography.
RESULTS: The injection of EP4 agonist alone did not induce notable changes in body weight, macro-structures, or bone volume compared with the vehicle-treated group or the untouched control side. EP4 agonist injection in conjunction with tooth movement significantly enhanced the amounts of tooth movement and regional bone volume in the tension side compared with the vehicle-treated group (P <.05).
CONCLUSIONS: Our preliminary study suggests the possibilities of synergistic enhancement of the rates of tooth movement and bone formation during tooth movement through the local injection of a specific EP4 receptor agonist. However, more study on the synergistic effect on tooth movement and bone formation in response to an EP4 agonist is needed to determine its mechanisms.

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Year:  2007        PMID: 17920491     DOI: 10.1016/j.ajodo.2007.02.049

Source DB:  PubMed          Journal:  Am J Orthod Dentofacial Orthop        ISSN: 0889-5406            Impact factor:   2.650


  4 in total

1.  Estrogen receptor α mediates proliferation of osteoblastic cells stimulated by estrogen and mechanical strain, but their acute down-regulation of the Wnt antagonist Sost is mediated by estrogen receptor β.

Authors:  Gabriel L Galea; Lee B Meakin; Toshihiro Sugiyama; Noureddine Zebda; Andrew Sunters; Hanna Taipaleenmaki; Gary S Stein; Andre J van Wijnen; Lance E Lanyon; Joanna S Price
Journal:  J Biol Chem       Date:  2013-01-29       Impact factor: 5.157

2.  Sost down-regulation by mechanical strain in human osteoblastic cells involves PGE2 signaling via EP4.

Authors:  Gabriel L Galea; Andrew Sunters; Lee B Meakin; Gul Zaman; Toshihiro Sugiyama; Lance E Lanyon; Joanna S Price
Journal:  FEBS Lett       Date:  2011-06-28       Impact factor: 4.124

3.  Tension force-induced bone formation in orthodontic tooth movement via modulation of the GSK-3β/β-catenin signaling pathway.

Authors:  Yelin Mao; Liangliang Wang; Ye Zhu; Yu Liu; Hongwei Dai; Jianping Zhou; Dechun Geng; Lin Wang; Yong Ji
Journal:  J Mol Histol       Date:  2017-12-09       Impact factor: 2.611

Review 4.  Is Inflammation a Friend or Foe for Orthodontic Treatment?: Inflammation in Orthodontically Induced Inflammatory Root Resorption and Accelerating Tooth Movement.

Authors:  Masaru Yamaguchi; Shinichi Fukasawa
Journal:  Int J Mol Sci       Date:  2021-02-27       Impact factor: 5.923

  4 in total

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