首页> 外文期刊>Natural product communications >Suppression of Release of Matrix Metalloprotease-1 from Human Gingival Fibroblasts by Cimicifuga Rhizome Extract and a Novel Cimigenol Xyloside as an Active Constituent
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Suppression of Release of Matrix Metalloprotease-1 from Human Gingival Fibroblasts by Cimicifuga Rhizome Extract and a Novel Cimigenol Xyloside as an Active Constituent

机译:Cimicifuga relizoma萃取物的人牙龈成纤维细胞与人牙龈成纤维细胞的释放抑制基质金属蛋白-1和作为活性组分的新型Cimigenol Xyloside

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摘要

Oral malodor has become a major oral problem and the need for self-medication has increased. Oral malodor is attributed to the various enzymes produced by periodontal bacteria and the treatment of periodontal disease is recognized as the major therapy for oral malodor. In our research program to investigate novel agents for alternative medicine, which are effective for oral malodor treatment, we focused on Cimicifuga rhizomes used in ancient Chinese medicine for the treatment of periodontal diseases. In order to evaluate the effectiveness of Cimicifuga rhizomes on periodontal disease, suppression of matrix metalloprotease-1 from human gingival fibroblasts was assayed. A 50% ethanol extract from Cimicifuga rhizomes showed 51.0% suppression at 10 mu g/mL. Activity-guided purification of the active principle was led to the isolation of 7,8-didehydrocimigenol 3-O-beta-D-xylopyranoside (1), 24-epi-24-O-acetyl-7,8-didehydrohydroshengmanol 3-O-beta-D-xylopyranoside (2) and a novel compound (3). Compound 3 was elucidated as 24,25-epoxy-7,8-didehydrohydroshengmanol 3-O-beta-D-xylopyranosidc by spectral analysis. Compounds 1 and 3 suppressed matrix metalloprotease-1 release at 50 nM. From these results, the extract from Cimicifuga rhizome may be a novel agent for oral malodor therapy as an alternative medicine.
机译:口腔恶臭已成为一个主要的口腔问题,需要自我用药的需求增加。口服恶臭归因于牙周细菌产生的各种酶,牙周病的治疗被认为是口服恶臭的主要治疗。在我们研究方案中调查替代医学的新药,这对于口服恶臭治疗有效,我们专注于古代中医用于治疗牙周病的Cimicifuga Rhizomes。为了评估Cimicifuga根茎对牙周病的有效性,测定来自人牙龈细胞的基质金属蛋白酶-1的抑制。来自Cimicifuga根茎的50%乙醇提取物,显示为10μg/ ml的51.0%抑制。活性原理的活动引导净化导致分离7,8-脱酰基丙烯3-O-β-D-氧化吡喃钠(1),24-EPI-24-O-乙酰基-7,8-二邻羟基氢莫诺尔3-O. -beta-d-氧化物(2)和新型化合物(3)。通过光谱分析,阐明化合物3为24,25-环氧-7,8-二脱羟基生蒽诺诺尔3-O-Beta-D- Xylopyranosidc。化合物1和3抑制基质金属蛋白酶-1释放在50nm。从这些结果来看,来自Cimicifuga Rhizome的提取物可以是作为替代医学的口服恶臭治疗的新试剂。

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