Effects of Glycyrrhizin on C6 Glioma Cells, with Special Reference to Cell Proliferation and Cell-Specific Proteins
        The bulletin of the Yamaguchi Medical School Volume 37 Issue 3-4
        Page 131-135
        
    published_at 1990-12
            Title
        
        Effects of Glycyrrhizin on C6 Glioma Cells, with Special Reference to Cell Proliferation and Cell-Specific Proteins
        
        
    
                
                    Creators
                
                    Nishizaki Takafumi
                
                
            
            
            
                
                    Creators
                
                    Orita Tetsuji
                
                
            
            
                
                    Creators
                
                    Ito Haruhide
                
                
            
            
                
                    Creators
                
                    Murakami Tomoyuki
                
                
            
            
                
                    Creators
                
                    Tanaka Kazunari
                
                
            
            
                
                    Creators
                
                    Takahashi Manabu
                
                
            
    
        
            Source Identifiers
        
    
    
            Creator Keywords
        
            Glycyrrhizin
            C6 glioma cell
            Cell proliferation
            Specific protein
    The effects of glycyrrhizin (GL) on cell proliferation, cell viability, and expression of cell-associated proteins, such as glial fibrillary acidic protein (GFAP), vimentin and S-100 protein, were estimated using an ethylnitrosourea (ENU)-elicited rat glioma cell line (C6). Graded concentrations of GL, 1.0, 1.5 and 2.0 mg/ml, were added individully to C6 cultures every 24 h and examined up to 72 hour. Cell viability was determined using a propidium iodide (PI) exclusion method. Cell cycle analyses were performed on the DNA histrogram using flow cytometry. We also investigated changes in the expression of proteins by the FITC/PI double-staining technique using flow cytometry. Cell proliferation was retarded and the number of the dead cells was increased dose-dependently by GL treatment. In cells treated with 1.0 or 1.5 mg/ml GL, cell-cycle alterations indicating an increase of the G0/G1 phase and a decrease of the S and G2M phases from the first day, were similar to those in the control group. In cells treated with 2.0 mg/ml GL, the fraction of G0/G1-phase cells did not increase, probably because the excessive dose of GL had an intense cytotoxic effect, resulting in paucity of cells in culture. These results suggest that cells were eventually lost from all phases of the cell cycle, in a dose-dependent manner and that the main effect of GL on cell proliferation was direct cytotoxicity. Maximum exposure to GL caused increased expression of each cell-specific protein, especially GFAP. However, no obvious clarification of the phenotypic alteration induced by GL treatment was obtained.
        
        
            Languages
        
            eng
    
    
        
            Resource Type
        
        departmental bulletin paper
    
    
        
            Publishers
        
            Yamaguchi University Graduate School of Medicine
    
    
        
            Date Issued
        
        1990-12
    
    
        
            File Version
        
        Version of Record
    
    
        
            Access Rights
        
        open access
    
    
            Relations
        
            
                
                
                [ISSN]0513-1812
            
            
                
                
                [NCID]AA00594272
            
    
        
            Schools
        
            医学部
    
                
