Literature DB >> 6401401

Histochemistry of enzymes associated with tissue degradation incident to orthodontic tooth movement.

E Lilja, S Lindskog, L Hammarström.   

Abstract

Orthodontic tooth movement in rats was examined by histochemical techniques for some enzymes associated with bone resorption and tissue damage. The maxillary first molar was moved buccally by means of a fixed appliance with predetermined forces for periods of from 10 hours to 6 days. The activities of acid phosphatase and lactate dehydrogenase were higher in cells in the connective tissue of the periodontal membrane (PDM) than in the oral mucosa. A low orthodontic force resulted in an initial redistribution of acid phosphatase-containing cells in the PDM followed by an increased activity of acid phosphatase. The activity of lactate dehydrogenase in the PDM was not affected by low orthodontic forces. The changes in distribution and activity of acid phosphatase and lactate dehydrogenase incident to a high orthodontic force were similar to those seen incident to a low force. However, there was one definite difference. A zone which lacked acid phosphatase activity and lactate dehydrogenase activity developed in the most compressed areas of the PDM. Prostaglandin synthetase activity was found exclusively in the bone marrow and seemed not to be affected by the orthodontic forces. However, some prostaglandin synthetase activity was found in the oral mucosa corresponding to the site of the orthodontic appliance. The adjacent bone surface was covered with cells showing an intense acid phosphatase activity. In the present study the magnitude of the orthodontic force seemed to be a determining factor for the vitality of the PDM but not for the tissue-degradation activity.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6401401     DOI: 10.1016/0002-9416(83)90273-7

Source DB:  PubMed          Journal:  Am J Orthod        ISSN: 0002-9416


  6 in total

1.  Demonstration of cells of the mononuclear phagocyte lineage in the periodontium following experimental tooth movement in the rat. An immunohistochemical study using monoclonal antibodies ED1 und ED2 on paraffin-embedded tissues.

Authors:  A Jäger; R J Radlanski; W Götz
Journal:  Histochemistry       Date:  1993-08

2.  Dietary lipids, prostaglandin E2 levels, and tooth movement in alveolar bone of rats.

Authors:  P P Kokkinos; R Shaye; B S Alam; S Q Alam
Journal:  Calcif Tissue Int       Date:  1993-11       Impact factor: 4.333

3.  M-CSF accelerates orthodontic tooth movement by targeting preosteoclasts in mice.

Authors:  Patricia J Brooks; Andrea F Heckler; Kuiru Wei; Siew-Ging Gong
Journal:  Angle Orthod       Date:  2011-03       Impact factor: 2.079

4.  Lactate dehydrogenase activity in gingival crevicular fluid as a marker in orthodontic tooth movement.

Authors:  Sarah A Alfaqeeh; Sukumaran Anil
Journal:  Open Dent J       Date:  2011-07-07

5.  Effect of orthodontic forces on levels of enzymes in gingival crevicular fluid (GCF): A systematic review.

Authors:  Priyanka Kapoor; Nitika Monga; Om Prakash Kharbanda; Sunil Kapila; Ragini Miglani; Rajeswari Moganty
Journal:  Dental Press J Orthod       Date:  2019-05-20

6.  Histopathologic investigation of the effects of prostaglandin E2 administered by different methods on tooth movement and bone metabolism.

Authors:  Murat Cağlaroğlu; Abdulvahit Erdem
Journal:  Korean J Orthod       Date:  2012-06-28       Impact factor: 1.372

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.