Journal of Agricultural and Food Chemistry · 2014 · 42 citations · 18 references
Life SciencesPharmacologyPhysiologyCell SignalingMetabolic RegulationSignal TransductionAdipocyte DifferentiationAdipose TissueLipid MetabolismMetabolic SignalingObesity ManagementWeight ManagementAdipocyte BiologyAdipocyte MetabolismAnimal Weight GainBody Weight RegulationClonal ExpansionCyclin RegulationIncreased AdiposityObesity Physiology
In the present study, we aimed to investigate the antiobesity effect of CAPE in vivo, and the mechanism by which CAPE regulates body weight in vitro. To confirm the antiobesity effect of CAPE in vivo, mice were fed with a high fat diet (HFD) with different concentrations of CAPE for 5 weeks. CAPE significantly reduced body weight gain and epididymal fat mass in obese mice fed a HFD. In accordance with in vivo results, Oil red O staining results showed that CAPE significantly suppressed MDI-induced adipogenesis of 3T3-L1 preadipocytes. FACS analysis results showed that CAPE delayed MDI-stimulated cell cycle progression, thereby contributing to inhibit mitotic clonal expansion (MCE), which is a prerequisite step for adipogenesis. Also, CAPE regulated the expression of cyclin D1 and the phosphorylation of ERK and Akt, which are upstream of cyclin D1. These results suggest that CAPE exerts an antiobesity effect in vivo, presumably through inhibiting adipogenesis at an early stage of adipogenesis.
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The Soy Isoflavone Genistein Decreases Adipose Deposition in Mice
Afia Naaz, Srikanth Yellayi, Melissa A. Zakroczymski et al. · Endocrinology · 2003 · 264 citations · Full text