Abstract | OBJECTIVE: MATERIALS AND METHODS: Twelve-week-old male Sprague-Dawley rats were divided into normal occlusion and occlusal hypofunction groups. After a 2-week bite-raising period, rat first molar was moved mesially using a 10-gf titanium- nickel alloy closed coil spring in both groups. On days 0, 1, 2, 3, and 7 after tooth movement, histologic changes were examined by micro-computed tomography and immunohistochemistry using CD31, VEGF-A, VEGFR-2, and the terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) method. RESULTS: Hypofunctional molars inclined more than normal molars and did not move notably after day 1 of tooth movement. Blood vessels increased on the tension side of the PDL in normal teeth. Immunoreactivities for VEGF-A and VEGFR-2 in normal teeth were greater than those in hypofunctional teeth during tooth movement. Compressive force rapidly caused apoptosis of the PDL and vascular endothelial cells in hypofunctional teeth, but not in normal teeth. CONCLUSIONS: Occlusal hypofunction induces vascular constriction through a decrease in the expression of VEGF-A and VEGFR-2, and apoptosis of the PDL and vascular cells occurs during tooth movement.
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Authors | Risa Usumi-Fujita, Jun Hosomichi, Noriaki Ono, Naoki Shibutani, Sawa Kaneko, Yasuhiro Shimizu, Takashi Ono |
Journal | The Angle orthodontist
(Angle Orthod)
Vol. 83
Issue 1
Pg. 48-56
(Jan 2013)
ISSN: 1945-7103 [Electronic] United States |
PMID | 22716278
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Vascular Endothelial Growth Factor A
- Vascular Endothelial Growth Factor Receptor-2
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Topics |
- Animals
- Immunohistochemistry
- In Situ Nick-End Labeling
- Male
- Malocclusion
(complications, pathology)
- Molar
(abnormalities, blood supply)
- Periodontal Atrophy
(etiology)
- Periodontal Ligament
(blood supply, metabolism, pathology)
- Rats
- Rats, Sprague-Dawley
- Stress, Mechanical
- Tooth Movement Techniques
(adverse effects, methods)
- Vascular Endothelial Growth Factor A
(metabolism)
- Vascular Endothelial Growth Factor Receptor-2
(metabolism)
- X-Ray Microtomography
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