Analysis for stimulation of GPR120 for osteoclast formation and orthodontic tooth movement
Project/Area Number |
16K20637
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Orthodontics/Pediatric dentistry
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Research Institution | Tohoku University |
Principal Investigator |
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Project Period (FY) |
2016-04-01 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
|
Keywords | GPR120 / DHA / 破骨細胞 / 破骨細胞形成 / 矯正学的歯の移動 |
Outline of Final Research Achievements |
PBS, LPS, LPS+DHA, LPS+DHA+AH7614, and DHA were injected subcutaneously on the calvariae of wild-type mice to confirm the LPS-induced osteoclast formation and the inhibitive effect of GPR 120 signaling pathway on LPS-induced osteoclast formation. After supracalvarial injections of reagents, mice were euthanized for preparing paraffin sections of mouse calvaria. TRAP staining was then performed to evaluate osteoclast formation in the suture mesenchyme. In the LPS injection group, many TRAP positive osteoclasts were induced. On the other hand, there was a significant reduction of osteoclast number in the LPS+DHA injection group. In addition, the inhibitive effect of DHA on osteoclast formation was suppressed by selective GPR120 antagonist AH7614, which was shown in the LPS+DHA+AH7614 injection group.
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Report
(3 results)
Research Products
(19 results)
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[Journal Article] Corrosion resistance and mechanical properties of titanium nitride plating on orthodontic wires2018
Author(s)
Sugisawa, H., Kitaura, H., Ueda, K., Kimura, K., Ishida, M., Ochi, Y., Kishikawa, A., Ogawa, S., Takano-Yamamoto T
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Journal Title
Dental Materials Journal
Volume: 37
Issue: 2
Pages: 286-292
DOI
NAID
ISSN
0287-4547, 1881-1361
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] Role of muramyl dipeptide for lipopolysaccharide-mediated biological activity and osteoclast activity.2018
Author(s)
Kitaura, H., Ishida, M., Kimura, K., Sugisawa, H., Kishikawa A, Shima, K., Ogawa S., Qi J, Kitaura H., Shen WR
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Journal Title
Anal. Cell. Pathol.
Volume: Volume 2018
Pages: 8047610-8047610
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Presentation] Inhibition of lipopolysaccharide-induced osteoclast formation and bone resorption in vivo by glucagon-like peptide-1 receptor agonist.2018
Author(s)
Shen WR, Kimura K, Ishida M, Kishikawa A, Shima K, Ogawa S, Qi J, Ohori F, Noguchi T, Marahleh A, Kitaura H.
Organizer
International Symposium for Multimodal Research and Education in IOHS-Liaison 2018
Related Report
Int'l Joint Research
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[Presentation] Comparisons with and without retention in orthodontic relapse mouse models.2018
Author(s)
Qi J, Kimura K, Ishida M, Kishikawa A, Shima K, Ogawa S, Shen WR, Ohori F, Noguchi T, Marahleh A, Kitaura H
Organizer
International Symposium for Multimodal Research and Education in IOHS-Liaison 2018
Related Report
Int'l Joint Research
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[Presentation] Exendin-4, a GLP-1 receptor agonist, suppresses inflammation-induced osteoclast formation and bone resorption2017
Author(s)
Shen WR, Kimura K, Ishida M, Sugisawa H, Ochi Y, Kishikawa A, Shima K, Ogawa S., Qi J, Kitaura H.
Organizer
The 12th International Workshop on Biomaterials in Interface Science. Innovative Research for Biosis-Abiosis Intelligent Interface Summer Seminar 2017
Related Report
Int'l Joint Research
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[Presentation] Analysis of friction oh titanium nitride plating on orthodontic wires.2016
Author(s)
Sugisawa H., Kitaura H., Ueda K., Kimura K., Ishida M., Ochi Y., Kishikawa A., Ogawa S., Takano-Yamamoto T.
Organizer
The 11th International Workshop on Biomaterials in Interface Science Innovative Research for Biosis-Abiosis Intelligent Interface Summer Seminar 2016.
Place of Presentation
バーデン家壮鳳(宮城県)
Year and Date
2016-08-30
Related Report
Int'l Joint Research