Fig. 1. The process of inducing cell adipogenesis and drug treatment.
Fig. 2. Rosemary extracts inhibited adipogenesis in the 3T3-L1 cell line. The 3T3-L1 cell line was maintained in DMEM containing 10% FBS, 25 mM NaHCO3 and 25 mM HEPEs (culture medium) and adipogenesis was induced with culture medium including 10 μM rosiglitazone, 10 μg/ml insulin and 1 μM dexamethasone (differentiation medium). All extracts were treated 50 μg/ml throughout the induction period. Cells were stained with oil red O for photography (A), after which the oil red O was dissolved using iso-propanol and the OD value was determined (B). Pictures were taken at 200× (A). Values are presented as the mean ± SD (n=3).
Fig. 3. Inhibitory effect of tyrosinase in Rosmarinus officinalis L. leaf and stem powder extracts. Kojic acid used as positive control is percent at 50 μg/ml. Results are presented as mean ± SD of three independent experiments.
Table 1. Inhibitory effect of DPPH scavenging in Rosmarinus officinalis L. leaf and stem powder extracts
Table 2. Inhibitory effect of α-glucosidase in Rosmarinus officinalis L. leaf and stem powder extracts
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