摘要
目的:探讨不同浓度淫羊藿苷、黄芩苷和大黄素对细菌内毒素脂多糖(lipopolysaccharide,LPS)刺激人牙龈成纤维细胞(human gingival fibroblasts,HGF)产生前列腺素E2(prostaglandin E2,PGE2)的影响。方法:以培养的人牙龈成纤维细胞为实验模型,用MTT试验检测淫羊藿苷、黄芩苷和大黄素抑制LPS对牙龈成纤维细胞毒性作用的效果,初步筛选其作用浓度;然后用酶联免疫法检测三种提取物对LPS刺激牙龈成纤维细胞产生重要的骨吸收因子PGE2的影响。结果:LPS对HGF有明显的细胞毒性,三种提取物均可显著提高细胞成活率。LPS作用6h后培养上清中PGE2含量上升,而同时加入淫羊藿苷、黄芩苷和大黄素各浓度组PGE2含量显著低于对照组(p<0.01)。结论:淫羊藿苷、黄芩苷和大黄素均可抑制LPS对HGF的细胞毒性作用,并且可抑制LPS刺激HGF产生PGE2。
Objective: To study the inhibitory effects of icariin, emodin and baicalin on human gingival fibroblasts (HGF) stimulated by the bacterial endotoxin lipopolysaccharide (LPS). Method: In this protocol, different conditions of emodin, baicalin and icariin were added to the culture of human gingival fibroblasts. MTF assay and enzyme-linked immunosorbent assay were used to examine the effects of these compounds on the inhibitory effects of the proliferation of human gingival fibroblast and the release of PGEz induced by E-LPS. Result: E-LPS show cytotoxity on HGF and, while each of these compounds can increase the cell survival rate significantly (p〈0.01). The quantity of PGEz of the cell culture media stimulated by E-LPS were significantly higher than added icariin, emodin or baicalin simultaneous (p〈0.01). Conclusion: The study suggests that the compound of icariin, emodin and baicalin can ameliorate the cytotoxity of E-LPS and inhibit the release of PGE2 by human gingival fibroblasts stimulated with E-LPS.
出处
《临床口腔医学杂志》
2009年第2期69-72,共4页
Journal of Clinical Stomatology