“…The underlying molecular mechanism was the activation of peroxisome proliferator-activated receptor (PPARr; Cho, Kim, Burgess, & Kim, 2006;Dang & Löwik, 2010;Sakamoto, Naka, Ohara, Kondo, & Iida, 2014), which modulated the expression of several key molecules involved in insulin signalling, lipid metabolism and endocrine function in adipocytes (Cho et al, 2006;Dang & Löwik, 2010;Sakamoto et al, 2014). On the other hand, some researchers reported that daidzein inhibited adipogenic differentiation and fat deposition (Cao, Zhang, Zou, & Xia, 2013;Kim et al, 2010;Rachoń, Vortherms, Seidlová-Wuttke, & Wuttke, 2007). They illuminated that daidzein had oestrogenic properties and could bind to oestrogen receptor α and β (ERα and ERβ, respectively; Dang, Audinot, Papapoulos, Boutin, & Löwik, 2003;Dang & Löwik, 2010), which were the ligand-activated transcription factors for inhibiting adipogenic differentiation (Cooke, Heine, Taylor, & Lubahn, 2001).…”