원문정보
초록
영어
Two flavonoids, isorhamnetin 3-O-β-D-glucopyranoside (1) and quercetin 3-O-β-D-glucopyranoside (2), from slander glasswort (Salicornia herbacea, Korean name hamcho) were isolated. Antioxidative and matrix metalloproteinase-9 (MMP-9) inhibitory effects of these compounds were investigated in HT 1080 cell lines. These compounds suppressed the
electron spin resonance (ESR) signal intensity on generation of 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical in a freecellular system. Their scavenging effects on generation of intercellular reactive oxygen species (ROS) also exhibited similar trends with DPPH radical in the free cellular system. Also, a control group combined only with Fe(II)-H2O2 resulted in DNA
apoptosis by oxidative stress, whereas treatments with these compounds suppressed radical-mediated DNA damage. Intracellular glutathione (GSH) levels were slightly increased in the presence of compound 1 and 2. Moreover, these compounds led to the reduction of the expression levels of MMP-9 without cytotoxic influence. These results suggest that these compounds have a potential as a valuable natural antioxidant and MMP inhibitor related to oxidative stress. Therefore, these compounds not only can be developed as a candidate for a therapeutic potential but also a source for use as ingredients of health foods or functional
foods to prevent metastasis involving MMP-9, closely related to ROS.
목차
Introduction
Materials and Methods
Plant material and isolation of compounds
Determination of DPPH radical scavenging activity byelectron spin resonance spectroscopy
Cell culture and cytotoxicity determination using MTTassay
Determination of intracellular formation of ROS usingDCF-DA labeling
Genomic DNA isolation
Determination of radical-mediated DNA damage
Measurement of intracellular GSH level
Determination of MMP activity by gelatin zymography
Statistical analysis
Results and Discussion
Scavenging activity on DPPH radicals
Cell viability
Cellular radical scavenging effect
Inhibitory effect on DNA oxidation
Regulation of GSH Level
Inhibition effect on MMP-9 activity
References