4.3 Article

Local administration of high-dose diabetes medicine exendin-4 inhibits orthodontic tooth movement in mice

期刊

ANGLE ORTHODONTIST
卷 91, 期 1, 页码 111-118

出版社

E H ANGLE EDUCATION RESEARCH FOUNDATION, INC
DOI: 10.2319/021320-103.1

关键词

Diabetes; GLP-1; Exendin-4; Osteoclast; Orthodontic tooth movement

资金

  1. JSPS KAKENHI grants from the Japan Society for the Promotion of Science [16K11776, 19K10397, 18K09862]
  2. Grants-in-Aid for Scientific Research [19K10397, 18K09862, 16K11776] Funding Source: KAKEN

向作者/读者索取更多资源

The study found that exendin-4 inhibits orthodontic tooth movement in mice, reduces root resorption, and affects the expression levels of osteoclast-related cytokines. Therefore, orthodontic patients receiving exendin-4 for diabetes treatment need additional attention during orthodontic treatment. The GLP-1 receptor may be a treatment target for patients with severe root resorption.
Objectives: To investigate the effects of exendin-4 on orthodontic tooth movement distance, root resorption, and expression levels of osteoclast-related cytokines in a mouse model. Materials and Methods: A 10-g NiTi coil spring was placed between the anterior alveolar bone and upper left first molar of 8-week-old male C57BL/6 mice. Twenty microliters of exendin-4 solution (containing 0.2 mu g, 4 mu g, or 20 mu g exendin-4) or phosphate-buffered saline (PBS) were injected on the buccal side of the upper left first molar at 2-day intervals (4 mice per group). Mice were sacrificed on day 12; silicone impressions were taken to record tooth movement distance. The left maxillae of the PBS and 20 mu g exendin-4 groups were also excised for histological analysis and quantitative reverse transcription polymerase chain reaction analysis. Results: Orthodontic tooth movement distance was smaller in the 20 mu g exendin-4 group than in the PBS group (P < .01). Compared with the PBS grouP < the 20 mu g exendin-4 group showed lower osteoclast number (P < .05), odontoclast number (P < .05), and root resorption surface percentage (P < .05). Relative to maxillae with PBS injections, maxillae with 20 mu g exendin-4 injections had lower receptor activator of nuclear factor kappa-B ligand (RANKL) mRNA expression (P < .05), TNF-alpha mRNA expression (P < .05), and RANKL/osteoprotegerin (OPG) ratio (P < .01). There were no differences in the expression of OPG mRNA. Conclusions: Exendin-4 inhibits orthodontic tooth movement. Therefore, additional attention is needed for orthodontic patients who receive exendin-4 for diabetes treatment. GLP-1 receptor may be a treatment target for patients with severe root resorption.

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