Literature DB >> 22141456

Effects of relaxin on relapse and periodontal tissue remodeling after experimental tooth movement in rats.

Yurie Hirate1, Masaru Yamaguchi, Kazutaka Kasai.   

Abstract

The relapse of teeth that have moved during orthodontic treatment is a major clinical issue with respect to the goals of successful treatment. Relaxin has an influence on many physiologic processes, such as collagen turnover. In this study, we determined the effects of relaxin on the relapse and remodeling of periodontal tissue after experimental tooth movement in rats, and we explored the molecular mechanism underlying these processes. To induce experimental tooth movement in rats, 10 g of orthodontic force was applied to the molars. After 14 days, the spring was removed, and then animals began receiving relaxin at a dose of 500 ng/ml for 1 week. The results were evaluated by micro-computed tomography and immunofluorescence staining. In addition, the effects of matrix metalloproteinase (MMP)-1 and MMP-8 production were investigated in human periodontal ligament (hPDL) cells in vitro. The expression of MMP-1 and MMP-8 was analyzed by real-time polymerase chain reaction and enzyme-linked immunosorbent assay. Furthermore, we demonstrated the signaling pathways involved in relaxin-regulated MMPs expression. The relapse distances and percentages were significantly decreased in the experimental group compared with the controls in vivo. A double-immunofluorescence analysis for Col-I/MMP-1 and Col-I/MMP-8 detected the expression of relaxin in the PDL. Relaxin significantly increased the MMP-1 and MMP-8 expression in a time-dependent manner in hPDL cells in vitro. Furthermore, a p38 inhibitor (SB203580) significantly inhibited the MMP-1 and MMP-8 expression. Our results indicated that relaxin modulates the collagen metabolism, and this hormone may therefore be useful to prevent orthodontic relapse following orthodontic treatment.

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Year:  2011        PMID: 22141456     DOI: 10.3109/03008207.2011.628060

Source DB:  PubMed          Journal:  Connect Tissue Res        ISSN: 0300-8207            Impact factor:   3.417


  6 in total

1.  Upregulation of relaxin receptors in the PDL by biophysical force.

Authors:  S Y Yang; J W Kim; S Y Lee; J H Kang; U Ulziisaikhan; H I Yoo; Y H Moon; J S Moon; H M Ko; M S Kim; S H Kim
Journal:  Clin Oral Investig       Date:  2014-07-05       Impact factor: 3.573

2.  Relaxin activates peroxisome proliferator-activated receptor γ (PPARγ) through a pathway involving PPARγ coactivator 1α (PGC1α).

Authors:  Sudhir Singh; Ronda L Simpson; Robert G Bennett
Journal:  J Biol Chem       Date:  2014-11-11       Impact factor: 5.157

3.  Antifibrotic effects of sulforaphane treatment on gingival elasticity reduces orthodontic relapse after rotational tooth movement in beagle dogs.

Authors:  Kyong-Nim Kim; Jue-Young Kim; Jung-Yul Cha; Sung-Hwan Choi; Jin Kim; Sung-Won Cho; Chung-Ju Hwang
Journal:  Korean J Orthod       Date:  2020-11-25       Impact factor: 1.372

4.  Raloxifene administration enhances retention in an orthodontic relapse model.

Authors:  Niloufar Azami; Po-Jung Chen; Shivam Mehta; Zana Kalajzic; Eliane H Dutra; Ravindra Nanda; Sumit Yadav
Journal:  Eur J Orthod       Date:  2020-09-11       Impact factor: 3.075

5.  Establishment of an orthodontic retention mouse model and the effect of anti-c-Fms antibody on orthodontic relapse.

Authors:  Jiawei Qi; Hideki Kitaura; Wei-Ren Shen; Akiko Kishikawa; Saika Ogawa; Fumitoshi Ohori; Takahiro Noguchi; Aseel Marahleh; Yasuhiko Nara; Itaru Mizoguchi
Journal:  PLoS One       Date:  2019-06-19       Impact factor: 3.240

6.  Ipriflavone promotes proliferation and osteogenic differentiation of periodontal ligament cells by activating GPR30/PI3K/AKT signaling pathway.

Authors:  Yuanyuan Han; Xuxia Wang; Dan Ma; Xiaoxiao Wu; Panpan Yang; Jun Zhang
Journal:  Drug Des Devel Ther       Date:  2018-01-11       Impact factor: 4.162

  6 in total

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