Suppr超能文献

组蛋白去乙酰化酶抑制剂与牙周骨丧失。

Histone deacetylase inhibitors and periodontal bone loss.

机构信息

Discipline of Anatomy and Pathology, School of Medical Sciences, University of Adelaide, Adelaide, SA, Australia.

出版信息

J Periodontal Res. 2011 Dec;46(6):697-703. doi: 10.1111/j.1600-0765.2011.01392.x. Epub 2011 Jul 11.

Abstract

BACKGROUND AND OBJECTIVE

Bone loss caused by enhanced osteoclast activity is a significant feature of periodontitis. Histone deacetylase inhibitors (HDACi) can suppress osteoclast-mediated bone loss in vitro and in vivo. This study investigated whether HDACi can suppress bone loss in experimental periodontitis.

MATERIAL AND METHODS

Experimental periodontitis was induced in mice by oral inoculation with Porphyromonas gingivalis bacteria. Mice were treated orally with olive oil alone, with olive oil and a novel compound - 1179.4b - which targets both Class I and Class II histone deacetylases (HDACs) or with olive oil and MS-275, which targets Class I HDACs. Micro-computed tomography scans of live mice, stereo imaging and histological analyses were used to detect changes in bone.

RESULTS

In the absence of treatment there was a 13.2% increase in bone volume in controls compared with a 7.4% decrease in P. gingivalis-inoculated mice. 1179.4b significantly reduced bone loss, with a 3.4% increase in bone volume (p < 0.01). MS-275 did not have a significant effect on P. gingivalis-induced bone loss. Histological analysis revealed that 1179.4b reduced bone loss despite having no effect on inflammation.

CONCLUSION

HDACi were found to effectively suppress bone loss in the mouse model of periodontitis. 1179.4b - the inhibitor of Class I and Class II HDACs - was more effective at suppressing bone loss than MS-275, which targets Class I HDACs only. These compounds may therefore have the potential to be used for the management of periodontitis.

摘要

背景与目的

破骨细胞活性增强导致的骨质流失是牙周炎的一个显著特征。组蛋白去乙酰化酶抑制剂(HDACi)可在体外和体内抑制破骨细胞介导的骨质流失。本研究旨在探讨 HDACi 是否可抑制实验性牙周炎中的骨质流失。

材料与方法

通过口腔接种牙龈卟啉单胞菌诱导小鼠发生实验性牙周炎。小鼠经口给予橄榄油单独处理、橄榄油与同时靶向 I 类和 II 类组蛋白去乙酰化酶(HDACs)的新型化合物 1179.4b 或仅靶向 I 类 HDACs 的 MS-275 联合处理。通过对活鼠进行微计算机断层扫描、体视学成像和组织学分析来检测骨变化。

结果

未经治疗时,与牙龈卟啉单胞菌接种组相比,对照组的骨体积增加了 13.2%,而接种组的骨体积减少了 7.4%。1179.4b 可显著减少骨质流失,骨体积增加了 3.4%(p<0.01)。MS-275 对牙龈卟啉单胞菌诱导的骨质流失无显著影响。组织学分析显示,尽管 1179.4b 对炎症无影响,但它可减少骨质流失。

结论

HDACi 可有效抑制牙周炎小鼠模型中的骨质流失。同时靶向 I 类和 II 类 HDACs 的 1179.4b 比仅靶向 I 类 HDACs 的 MS-275 更能抑制骨质流失。这些化合物因此可能具有用于治疗牙周炎的潜力。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验