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羟基磷灰石和鞣花酸在骨生成中的作用。

Role of Hydroxyapatite and Ellagic Acid in the Osteogenesis.

作者信息

Wardhana Agung Satria, Nirwana Intan, Budi Hendrik Setia, Surboyo Meircurius Dwi Condro

机构信息

Department of Dental Material, Faculty of Dentistry, Universitas Lambung Mangkurat, Banjarmasin, Indonesia.

Department of Dental Material, Faculty of Dental Medicine, Universitas Airlangga, Surabaya, Indonesia.

出版信息

Eur J Dent. 2021 Feb;15(1):8-12. doi: 10.1055/s-0040-1714039. Epub 2020 Jul 20.

Abstract

OBJECTIVE

Ellagic acid (EA), a phenolic antioxidant, has benefits in bone health and wound healing. The combination of EA and hydroxyapatite (HA) (EA-HA) is expected to increase osteogenesis. The aim of this study was to analyze osteogenesis after application of EA-HA according to the number of osteoblasts and osteoclasts in the bone and the expression of the receptor activator of nuclear factor kappa-B ligand (RANKL), osteoprotegerin (OPG), and osteocalcin (OCN) protein.

MATERIALS AND METHODS

Thirty Wistar rats were assessed with bone defects created in the left femur. The defects were filled with EA-HA and then sutured. Control groups were filled with polyethylene glycol (PEG) or HA. Each group was sacrificed either 7 or 14 days after treatment.

RESULTS

The defects filled with EA-HA exhibited the highest number of osteoblasts and the greatest expression of OPG and OCN at both day 7 and day 14 ( = 0.000). Conversely, treatment with EA-HA resulted in lower numbers of osteoclasts and reduced RANKL staining at both time points ( = 0.000).

CONCLUSIONS

EA-HA can increase osteogenesis in bone defects by increasing the number of osteoblasts and the expression of OPG and OCN.

摘要

目的

鞣花酸(EA)是一种酚类抗氧化剂,对骨骼健康和伤口愈合有益。EA与羟基磷灰石(HA)的组合(EA-HA)有望促进成骨作用。本研究的目的是根据骨中成骨细胞和破骨细胞的数量以及核因子κB受体活化因子配体(RANKL)、骨保护素(OPG)和骨钙素(OCN)蛋白的表达,分析应用EA-HA后的成骨情况。

材料与方法

对30只Wistar大鼠的左股骨制造骨缺损并进行评估。缺损处填充EA-HA后缝合。对照组填充聚乙二醇(PEG)或HA。每组在治疗后7天或14天处死。

结果

在第7天和第14天,填充EA-HA的缺损处成骨细胞数量最多,OPG和OCN的表达也最强(P = 0.000)。相反,在两个时间点,EA-HA治疗均导致破骨细胞数量减少和RANKL染色降低(P = 0.000)。

结论

EA-HA可通过增加成骨细胞数量以及OPG和OCN的表达来促进骨缺损处的成骨作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bd3/7906838/8073e7cb5b54/10-1055-s-0040-1714039_00652_01.jpg

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