論文

2014年8月

Selective β2-adrenergic antagonist butoxamine reduces orthodontic tooth movement

Journal of Dental Research
  • T. Sato
  • ,
  • K. Miyazawa
  • ,
  • Y. Suzuki
  • ,
  • Y. Mizutani
  • ,
  • S. Uchibori
  • ,
  • R. Asaoka
  • ,
  • M. Arai
  • ,
  • A. Togari
  • ,
  • S. Goto

93
8
開始ページ
807
終了ページ
812
記述言語
掲載種別
研究論文(学術雑誌)
DOI
10.1177/0022034514536730

Recently, involvement of the sympathetic nervous system in bone metabolism has attracted attention. β2-Adrenergic receptor (β2-AR) is presented on osteoblastic and osteoclastic cells. We previously demonstrated that β-AR blockers at low dose improve osteoporosis with hyperactivity of the sympathetic nervous system via β2-AR blocking, while they may have a somewhat inhibitory effect on osteoblastic activity at high doses. In this study, the effects of butoxamine (BUT), a specific β2-AR antagonist, on tooth movement were examined in spontaneously hypertensive rats (SHR) showing osteoporosis with hyperactivity of the sympathetic nervous system. We administered BUT (1 mg/kg) orally, and closed-coil springs were inserted into the upper-left first molar. After sacrifice, we calculated the amount of tooth movement and analyzed the trabecular microarchitecture and histomorphometry. The distance in the SHR control was greater than that in the Wistar-Kyoto rat group, but no significant difference was found in the SHR treated with BUT compared with the Wistar-Kyoto rat control. Analysis of bone volume per tissue volume, trabecular number, and osteoclast surface per bone surface in the alveolar bone showed clear bone loss by an increase of bone resorption in SHR. In addition, BUT treatment resulted in a recovery of alveolar bone loss. Furthermore, TH-immunoreactive nerves in the periodontal ligament were increased by tooth movement, and BUT administration decreased TH-immunoreactive nerves. These results suggest that BUT prevents alveolar bone loss and orthodontic tooth movement via β2-AR blocking. © International & American Associations for Dental Research.

リンク情報
DOI
https://doi.org/10.1177/0022034514536730
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/24868013
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84905816349&origin=inward
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84905816349&origin=inward
ID情報
  • DOI : 10.1177/0022034514536730
  • ISSN : 0022-0345
  • eISSN : 1544-0591
  • PubMed ID : 24868013
  • SCOPUS ID : 84905816349

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