The expression of nitric oxide synthetase in the experimental tooth movement in rats.
- Author:
Dong Kwon PARK
1
;
Sang Cheol KIM
Author Information
1. Department of Orthodontics, College of Dentistry, Wonkwang University, Korea. sangkim@wonkwang.ac.kr
- Publication Type:Original Article
- Keywords:
tooth movement;
nitric oxide(NO);
nitric oxide synthetase(NOS)
- MeSH:
Animals;
Calcium;
Calmodulin;
Capillaries;
Dental Cementum;
Dentin;
Gingiva;
Incisor;
Nitric Oxide Synthase*;
Nitric Oxide*;
Nitrous Oxide;
Odontoblasts;
Osteoblasts;
Osteoclasts;
Osteocytes;
Periodontal Ligament;
Periodontium;
Rats*;
Rats, Sprague-Dawley;
Streptavidin;
Sutures;
Tooth Movement*;
Tooth*
- From:Korean Journal of Orthodontics
2001;31(1):107-120
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Nitric oxide(NO) has been reported to be one of the mediators relating to bone remodelling. Nitric oxide is synthesized from L-arguinine by nitric oxide synthetase(NOS), which is largely divided into two groups. One group which is composed of NOS1 and NOS3, is dependent of calcium or calmodulin. The other consisted of NOS2, which is independent of calcium or calmodulin. NOS is thought to be a possible intermediate affecting in the course of tooth movement. This study was designed to evaluate the expression of nitrous oxide synthetase(NOS) in periodontal tissue during the experimental movement of rat incisors, by LSAB(labelled streptavidine biotin) immunohistochemical staining for NOS2 and NOS3. Twenty seven Sprague-Dawley rats were divided into a control group(3 rats), and 6 experimental groups(24 rats), to which 75g of force was applied, with helical springs across the maxillary incisors. Rats of experimental groups were sacrificed at 12 hours, 1, 4, 7, 14 and 28 days after force application, respectively. After that, the tissues of the control group and experimental groups were studied immunohistochemically. The results were as follows: 1. In control group, the expression of NOS3 was rare in gingiva, dentin, periodontal ligament and alveolar bone, and was mild in the capillaries of pulp and intermaxillary suture. And the expression of NOS2 showed similar pattern to that of NOS3. 2. There were no differences in the expression of NOS2 or NOS3 in dentin, gingiva, cementum, cementoblast and odontoblast, between control and experimental groups, regardless of the duration of the force application. 3. The expression of NOS3 began to increase at 4 days and showed to the highest degree at 7 days after force application, in the apical region of pressure side of periodontal ligament in experimental groups. 4. The expression of NOS3 in alveolar bone was rare until 7 days, after which it increased to mild degree at 14 days through 28 days in experimental group. But there was no difference between pressure and tension side of periodontal ligament. 5. The expression of NOS2 in periodontal ligament was mild from 7 days after force application, regardless of the side of periodontium, which was generally more evident than that of NOS3 . 6. The expression of NOS2 in alveolar bone increased to mild degree at 14 days after force application, and it was evident in osteoblasts, osteoclasts and osteocytes. And the expression of NOS2 was little more stronger in the tension side than that of pressure side of alveolar bone.
