Journal: Frontiers in Pharmacology
Article Title: Development of an adipocyte differentiation protocol using 3T3-L1 cells for the investigation of the browning process: identification of the PPAR-γ agonist rosiglitazone as a browning reference drug
doi: 10.3389/fphar.2025.1546456
Figure Lengend Snippet: Analysis of the activity of the citrate synthase enzyme representing the metabolic and mitochondrial activity of adipocyte cells at different differentiation times and following the different treatments used. (A) Enzyme activity stratified by time (T0, T3, T10, and T17) and by treatment (RGZ 0.1 μM, RGZ 1 μM, ISO 0.1 μM, and ISO 1 μM). (B) Representation of the variation of enzymatic activity as a function of time and stratified by treatment (RGZ 0.1 μM, RGZ 1 μM, ISO 0.1 μM, and ISO 1 μM). Graphs display the citrate synthase activity expressed in mU/mL ± SEM. Statistical significance versus WHITE T17 (**p < 0.01; ****p < 0.0001) in (A) . Statistical significance versus WHITE (*p < 0.05; **p < 0.01) in (B) . Abbreviations: ISO, isoproterenol; RGZ, rosiglitazone. Sample size (n): six for white T3, five for white T10, eight biological replicates for white T17; five biological replicates for RGZ 0.1 μM, RGZ 1 μM, ISO 0.1 μM, and ISO 1 μM at T3 and T10; 11 biological replicates for RGZ 0.1 μM and RGZ 1 μM at T17, and five biological replicates for ISO 0.1 μM and ISO 1 μM at T17. Three technical replicates per sample.
Article Snippet: RGZ (Merck KGaA, Germany) and ISO (Merck KGaA, Germany) at concentrations of 0.1 μM and 1 μM was added to both DM and MM to evaluate their impact on the de novo browning process.
Techniques: Activity Assay