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  Indian J Med Microbiol
 

Figure 3: Suppression of adipocyte differentiation by betulinic acid chalcone. The adipocytes were treated with dimethyl sulfoxide (control), rosiglitazone, and 2-, 4-, 8-, and 16-μM betulinic acid chalcone. The adipocyte differentiation was examined at 24 h of betulinic acid chalcone treatment using the Oil Red O staining assay by BX50 microscope (Olympus Corporation, Tokyo, Japan). Data are obtainable as the means ± standard deviation (n = 6) (*P < 0.05, **P < 0.01, and ***P < 0.001 vs. control group)

Figure 3: Suppression of adipocyte differentiation by betulinic acid chalcone. The adipocytes were treated with dimethyl sulfoxide (control), rosiglitazone, and 2-, 4-, 8-, and 16-μM betulinic acid chalcone. The adipocyte differentiation was examined at 24 h of betulinic acid chalcone treatment using the Oil Red O staining assay by BX50 microscope (Olympus Corporation, Tokyo, Japan). Data are obtainable as the means ± standard deviation (<i>n </i>= 6) (*<i>P </i>< 0.05, **<i>P </i>< 0.01, and ***<i>P </i>< 0.001 vs. control group)