Anti-MMP-2 and MMP-9 activity of Salsola komarovii Iljin extract and its solvent fractions

被引:0
|
作者
Kil, Jung-Ha [1 ]
Karadeniz, Fatih [1 ]
Yu, Ga [2 ]
Kim, Hojun [3 ]
Kim, Junse [3 ]
Oh, Jung Hwan [1 ]
Lee, Jung Im [1 ]
Kong, Chang-Suk [1 ,2 ]
Seo, Youngwan [3 ]
机构
[1] Silla Univ, Marine Biotechnol Ctr Pharmaceut & Foods, Baegyang Daero 700,Beon Gil 140, Busan 46958, South Korea
[2] Silla Univ, Dept Food & Nutr, Coll Med & Life Sci, Baegyang Daero 700,Beon Gil 140, Busan 46958, South Korea
[3] Korea Maritime & Ocean Univ, Div Marine Biosci, Busan 49112, South Korea
基金
新加坡国家研究基金会;
关键词
MATRIX-METALLOPROTEINASE INHIBITORS; MARINE NATURAL-PRODUCTS; CELLS; CONSTITUENTS; CANCER;
D O I
10.4103/2221-1691.290871
中图分类号
R188.11 [热带医学];
学科分类号
摘要
Objective: To investigate matrix metalloproteinases (MMP)-2 and MMP-9 inhibitory effect of Salsola komarovii Iljin, an edible halophyte with health beneficial effects. Methods: Salsola komarovii crude extracts (SKI), and solvent (n-hexane, 85% aq. MeOH, n-BuOH, and H2O) fractionated extracts of SKI were prepared. Gelatin zymography was carried out to observe MMP enzymatic activity. The release of the MMP enzymes was measured by enzyme-linked immunosorbent assay. Expression of MMPs in mRNA and protein level were investigated by polymerase chain reaction analysis and immunoblotting, respectively. Results: SKI and SKI fractions inhibited active MMP-2 and MMP-9 amount in the treated cell culture medium. Also, SKI suppressed the release of MMP-2 and MMP-9 from stimulated HT1080 human fibrosarcoma cells. Furthermore, SKI suppressed the mRNA and protein expression of MMP-2 and MMP-9. SKI fractions showed parallel effects except for H2O fraction which did not yield any significant MMP inhibitory effect. Among fractions, 85% aq. MeOH was the most active fraction to inhibit both the enzymatic effect and expression of MMP-2 and MMP-9. Conclusions: SKI may contain potential MMP release inhibitory compounds. Salsola komarovii is a promising source of compounds against MMP and could be utilized in the development of antitumor agents.
引用
收藏
页码:460 / 469
页数:10
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