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泗水分离株来源的脂多糖对牙槽骨破坏的影响。

Effect of lipopolysaccharide derived from surabaya isolates on alveolar bone destruction.

作者信息

Ridwan Rini Devijanti, Kusumaningsih Tuti, Salim Sherman

机构信息

Department of Oral Biology, Faculty of Dental Medicine, Universitas Airlangga, Surabaya, Indonesia.

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

出版信息

Vet World. 2018 Feb;11(2):161-166. doi: 10.14202/vetworld.2018.161-166. Epub 2018 Feb 10.

Abstract

BACKGROUND

lipopolysaccharide (LPS) has a high virulence factor. It interacts with serum protein through receptors on the epithelial cell surface, thereby increasing both interleukin (IL)-1β, and IL-6 which results in damage to periodontal tissue.

AIM

The aim of the study was to identify and evaluate the effect of LPS derived from local isolates ( on the destruction of alveolar bone by means of several biomarkers, including; the number of osteoblasts and osteoclasts, the expression of IL-6, matrix metallopeptidase 1 (MMP-1), and receptor activator of nuclear factor kappa-Β ligand (RANKL).

MATERIALS AND METHODS

The isolation of LPS from was calculated using phenol, while purification was performed using Sephadex C-18 column chromatography. 40 Wistar rats were divided into four groups of 10. Each treatment was divided into two groups which were 0.9% NaCl and LPS induced for 7 and 14 days, respectively. Gingival and alveolar bones were further introduced into the induction area, followed by the measuring of osteoblast and osteoclast with hematoxylin-eosin staining, IL-6, MMP-1 and RANKL expression with immunohistochemical.

RESULTS

Reduced numbers of osteoblasts at the 7 and 14 day of treatment were detected, while those of osteoclasts increased. There was an increased expression of IL-6, MMP-1, and RANKL in the 7 and 14-day treatment group. Treatment of LPS from over 7 and 14 days resulted in damage to periodontal tissue and alveolar bone in Wistar rats.

CONCLUSION

LPS of administration for 7 and 14 days causes periodontal and alveolar tissue destruction in Wistar rats.

摘要

背景

脂多糖(LPS)是一种高毒力因子。它通过上皮细胞表面的受体与血清蛋白相互作用,从而增加白细胞介素(IL)-1β和IL-6的水平,进而导致牙周组织损伤。

目的

本研究旨在通过多种生物标志物,包括成骨细胞和破骨细胞的数量、IL-6、基质金属蛋白酶1(MMP-1)和核因子κB受体激活剂配体(RANKL)的表达,来鉴定和评估本地分离株来源的LPS对牙槽骨破坏的影响。

材料与方法

使用苯酚计算从……中分离LPS的量,同时使用Sephadex C-18柱色谱法进行纯化。40只Wistar大鼠分为四组,每组10只。每种处理分为两组,分别用0.9%氯化钠和LPS诱导7天和14天。将牙龈和牙槽骨进一步引入诱导区域,随后用苏木精-伊红染色测量成骨细胞和破骨细胞,用免疫组织化学法测量IL-6、MMP-1和RANKL的表达。

结果

在治疗的第7天和第14天检测到成骨细胞数量减少,而破骨细胞数量增加。在7天和14天治疗组中,IL-6、MMP-1和RANKL的表达增加。7天和14天给予……来源的LPS治疗导致Wistar大鼠牙周组织和牙槽骨损伤。

结论

给予7天和14天的……LPS会导致Wistar大鼠牙周和牙槽组织破坏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6962/5891868/b44bdbd9e596/VetWorld-11-161-g001.jpg

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