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环氧化酶1和2选择性抑制剂全身及局部给药在大鼠牙周病实验模型中的作用

Role of systemic and local administration of selective inhibitors of cyclo-oxygenase 1 and 2 in an experimental model of periodontal disease in rats.

作者信息

Queiroz-Junior C M, Pacheco C M F, Maltos K L M, Caliari M V, Duarte I D G, Francischi J N

机构信息

Department of Pharmacology, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.

出版信息

J Periodontal Res. 2009 Apr;44(2):153-60. doi: 10.1111/j.1600-0765.2007.01069.x. Epub 2009 Feb 6.

Abstract

BACKGROUND AND OBJECTIVE

Periodontal disease is an inflammatory condition of tooth-supporting tissues. Arachidonic acid metabolites have been implicated in development of periodontal disease, especially those derived from the cyclo-oxygenase (COX) pathway. This study investigated the role of inhibitors of cyclo-oxygenases (COX-1 and COX-2) in a model of periodontal disease in rats.

MATERIAL AND METHODS

A ligature was placed around the molar of rats. Losses of fiber attachment and of alveolar bone were measured morphometrically in histologically prepared sections. Infiltration of cells into gingival tissue surrounding the ligated tooth was also determined.

RESULTS

Systemic and local administration of non-selective and selective COX-2 inhibitors, preventively, resulted in significant reduction of the losses of fiber attachment and alveolar bone, as well as decreased leukocyte numbers in gingival tissue. Preventive selective inhibition of COX-1 was as effective as COX-2 inhibition in reducing local fiber attachment loss and cell migration, but did not prevent alveolar bone loss.

CONCLUSION

Our results provide evidence for participation of COX-1 and COX-2 in early stages of periodontal disease in rats. Furthermore, local administration of COX inhibitors reduced the signs of periodontal disease to the same extent as systemic treatment. Therapeutic approaches incorporating locally delivered anti-inflammatory drugs could be of benefit for patients suffering from periodontal disease.

摘要

背景与目的

牙周病是牙齿支持组织的一种炎症性疾病。花生四烯酸代谢产物与牙周病的发展有关,尤其是那些源自环氧化酶(COX)途径的代谢产物。本研究调查了环氧化酶(COX - 1和COX - 2)抑制剂在大鼠牙周病模型中的作用。

材料与方法

在大鼠的磨牙周围放置结扎线。在组织学制备的切片上通过形态计量学测量纤维附着丧失和牙槽骨丧失。还测定了细胞向结扎牙齿周围牙龈组织的浸润情况。

结果

预防性全身和局部给予非选择性和选择性COX - 2抑制剂,可显著减少纤维附着丧失和牙槽骨丧失,以及牙龈组织中白细胞数量的减少。预防性选择性抑制COX - 1在减少局部纤维附着丧失和细胞迁移方面与抑制COX - 2效果相同,但不能预防牙槽骨丧失。

结论

我们的结果为COX - 1和COX - 2参与大鼠牙周病早期阶段提供了证据。此外,局部给予COX抑制剂与全身治疗在减轻牙周病症状方面程度相同。采用局部递送抗炎药物的治疗方法可能对牙周病患者有益。

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