Close
  Indian J Med Microbiol
 

Figure 2: Cytotoxic effects of YGSHT extract in undifferentiated and differentiated 3T3-L1 cells. (a) 3T3-L1 preadipocytes were treated with various concentrations of YGSHT (0, 7.8125, 15.625, 31.25, 62.5, 125, 250, or 500 μg/ml) for 24 h. (b) 3T3-L1 preadipocytes were differentiated into adipocytes by incubation with MDI for 8 days. The cells were exposed to various concentrations of YGSHT (0, 31.25, 62.5, 125, 250, 500 or 1000 μg/ml) during the differentiation period. Cell viability was determined using a CCK-8 assay kit by measuring the absorbance at 450 nm. Data are presented as mean SEM

Figure 2: Cytotoxic effects of YGSHT extract in undifferentiated and differentiated 3T3-L1 cells. (a) 3T3-L1 preadipocytes were treated with various concentrations of YGSHT (0, 7.8125, 15.625, 31.25, 62.5, 125, 250, or 500 μg/ml) for 24 h. (b) 3T3-L1 preadipocytes were differentiated into adipocytes by incubation with MDI for 8 days. The cells were exposed to various concentrations of YGSHT (0, 31.25, 62.5, 125, 250, 500 or 1000 μg/ml) during the differentiation period. Cell viability was determined using a CCK-8 assay kit by measuring the absorbance at 450 nm. Data are presented as mean SEM