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与正畸牙齿移动所致组织降解相关的酶的组织化学

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

作者信息

Lilja E, Lindskog S, Hammarström L

出版信息

Am J Orthod. 1983 Jan;83(1):62-75. doi: 10.1016/0002-9416(83)90273-7.

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.

摘要

通过组织化学技术,对大鼠正畸牙齿移动过程中一些与骨吸收和组织损伤相关的酶进行了检测。利用固定矫治器以预定的力使上颌第一磨牙颊向移动,时间从10小时至6天不等。牙周膜(PDM)结缔组织细胞中的酸性磷酸酶和乳酸脱氢酶活性高于口腔黏膜中的细胞。低正畸力导致PDM中含酸性磷酸酶细胞的初始重新分布,随后酸性磷酸酶活性增加。低正畸力对PDM中乳酸脱氢酶的活性没有影响。高正畸力引起的酸性磷酸酶和乳酸脱氢酶分布及活性变化与低正畸力时相似。然而,存在一个明显差异。在PDM最受压区域形成了一个缺乏酸性磷酸酶活性和乳酸脱氢酶活性的区域。前列腺素合成酶活性仅在骨髓中发现,似乎不受正畸力影响。然而,在与正畸矫治器部位相对应的口腔黏膜中发现了一些前列腺素合成酶活性。相邻骨表面覆盖着显示强烈酸性磷酸酶活性的细胞。在本研究中,正畸力的大小似乎是PDM活力的决定因素,但不是组织降解活性的决定因素。

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