4.7 Article

Inhibitory effect of phenolic acids on the proliferation of 3T3-L1 preadipocytes in relation to their antioxidant activity

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 54, Issue 12, Pages 4191-4197

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jf0609882

Keywords

phenolic acid; preadipocytes; proliferation; antiobesity; antioxidant activity

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Obesity is an important topic in the world of public health and preventive medicine. Inhibition of preadipocyte proliferation plays an important role in the mechanisms of proposed antiobesity. In this in vitro study, the inhibitory effect of phenolic acids on 3T3-L1 preadipocytes was evaluated, and a relationship analysis was then conducted. The results showed that the addition of phenolic acids to the growth medium decreased the cell population growth of 3T3-L1 preadipocytes. The IC50 values of chlorogenic acid, gallic acid, o- coumaric acid and m-coumaric acid on 3T3-L1 preadipocytes were 72.3, 43.3, 48.2, and 49.2 mu M, respectively. A relationship analysis indicated that there is a significant linear correlation between the influence of phenolic acids on cell population growth and their antioxidant activity (r=0.77, p < 0.01). The cell cycle assay indicated that the treatment of 3T3-L1 preadipocytes with chlorogenic acid, o- coumaric acid, and m-coumaric acid caused cell cycle arrest in the G(1) phase. Gallic acid did not affect the cell cycle profile; however, it increased the number of apoptotic cells (sub-G(1) phase) in a time- and dose- dependent manner. Annexin V- fluorescein isothiocyanate (FITC) propidium iodide (PI) apoptosis flow cytometric assay showed that gallic acid increased the number of early apoptotic (annexin-FITC+/ PI-) and late apoptotic cells (annexin V-FITC+/ PI+) but not necrotic cells (annexin V- FITC-/PI+). The treatment of cells with gallic acid caused the loss of mitochondrial membrane potential (Delta Psi(m)). These results indicate that the inhibition of preadipocyte population growth by some phenolic acids might have further implication in in vivo antiobesity effects.

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