La Vu Dang, Bergeron Chantal, Gafner Stefan, Grenier Daniel
Research Group in Oral Ecology, Faculty of Dentistry, Laval University, Quebec City, QC, Canada.
J Periodontol. 2009 Nov;80(11):1875-82. doi: 10.1902/jop.2009.090251.
Matrix metalloproteinases (MMPs) produced by resident and inflammatory cells in response to Gram-negative periodontopathogens play a major role in the tissue destruction observed during periodontitis, a disease that affects tooth-supporting structures. In this study, we investigated the effect of grape seed extract (GSE) on MMP secretion by human monocyte-derived macrophages stimulated with Aggregatibacter actinomycetemcomitans (previously Actinobacillus actinomycetemcomitans) lipopolysaccharide (LPS) and on the activity of human recombinant MMP-1 and -9.
Macrophages were treated with various concentrations of GSE prior to being stimulated with A. actinomycetemcomitans LPS. The secretion of MMPs and activation of nuclear factor-kappa B (NF-kappaB) p65 and activator protein-1 (AP-1) were assessed by enzyme-linked immunosorbent assay (ELISA). The effect of GSE on the catalytic activity of human recombinant MMP-1 and -9 was tested using fluorogenic assays.
GSE inhibited the secretion of MMP-1, -3, -7, -8, -9, and -13 by LPS-stimulated macrophages in a concentration-dependent manner. The suppression of MMP secretion was associated with inhibition of NF-kappaB p65 and AP-1 activation. Also, GSE dose-dependently inhibited the activity of MMP-1 and -9.
The present study suggests that GSE may be potentially used in the development of novel host-modulating strategies for the treatment of MMP-mediated disorders such as periodontitis.
驻留细胞和炎症细胞响应革兰氏阴性牙周病原体产生的基质金属蛋白酶(MMPs)在牙周炎(一种影响牙齿支持结构的疾病)期间观察到的组织破坏中起主要作用。在本研究中,我们调查了葡萄籽提取物(GSE)对牙龈卟啉单胞菌(以前称为伴放线放线杆菌)脂多糖(LPS)刺激的人单核细胞衍生巨噬细胞分泌MMPs的影响以及对人重组MMP-1和-9活性的影响。
在用牙龈卟啉单胞菌LPS刺激之前,用不同浓度的GSE处理巨噬细胞。通过酶联免疫吸附测定(ELISA)评估MMPs的分泌以及核因子-κB(NF-κB)p65和激活蛋白-1(AP-1)的激活。使用荧光测定法测试GSE对人重组MMP-1和-9催化活性的影响。
GSE以浓度依赖的方式抑制LPS刺激的巨噬细胞分泌MMP-1、-3、-7、-8、-9和-13。MMP分泌的抑制与NF-κB p65和AP-1激活的抑制相关。此外,GSE剂量依赖性地抑制MMP-1和-9的活性。
本研究表明,GSE可能潜在地用于开发新型宿主调节策略,以治疗诸如牙周炎等MMP介导的疾病。