Taxvig, Camilla1; Specht, Ina Olmer3; Boberg, Julie1; Vinggaard, Anne Marie4; Nellemann, Christine Lydia1
1 National Food Institute, Technical University of Denmark2 Division of Toxicology and Risk Assessment, National Food Institute, Technical University of Denmark3 Technical University of Denmark4 Copenhagen Center for Health Technology, Center, Technical University of Denmark
Phytoestrogens (PEs) are naturally occurring plant components, with the ability to induce biological responses in vertebrates by mimicking or modulating the action of endogenous hormones.Single isoflavones have been shown to affect adipocyte differentiation, but knowledge on the effect of dietary relevant mixtures of PEs, including for instance lignans, is lacking. In the current study dietary relevant mixtures of isoflavones and their metabolites, lignans and their metabolites, coumestrol, and a mixture containing all of them, were examined for effects on adipogenesis in 3T3-L1 adipocytes, as well as tested for their PPARγ activating abilities. The results showed that mixtures of isoflavonoid parent compounds and metabolites, respectively, a mixture of lignan metabolites, as well as coumestrol concentration-dependently inhibited adipocyte differentiation. Furthermore, a mixture of isoflavonoid parent compounds, and a mixture of isoflavonoid metabolites were found to have PPARγ activating abilities.These results suggest that PEs can affect pathways known to play a role in obesity development, and indicate that the inhibitory effect on adipocyte differentiation does not appear to be strictly associated with PPARγ activation/inhibition.The current study support the hypothesis that compounds with endocrine activity can affect pathways playing a role in the development obesity and obesity related diseases.
Food and Chemical Toxicology, 2013, Vol 55, p. 265-271
Phytoestrogens; 3T3-L1; Adipocyte differentiation; PPARγ; In vitro; Journal Article; Research Support, Non-U.S. Gov't; 3T3-L1 Cells; Adipocytes; Animals; Cell Differentiation; Diet; In Vitro Techniques; Mice; PPAR gamma