Saringosterol, a
steroid isolated from Sargassum muticum, a brown edible alga widely distributed on the seashores of southern and eastern Korea, has been shown to exhibit anti-
obesity effect. In this study, we investigated the anti-
obesity activity of
saringosterol through various experiments. The inhibitory effect of
saringosterol on adipogenesis was evaluated via
Oil Red O staining in 3T3-L1 preadipocytes. After confirming that
saringosterol is not cytotoxic to these cells by using the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium
bromide assay, the effect of
saringosterol on the expression of various adipogenesis-related genes was analyzed via quantitative real-time polymerase chain reaction and western blotting. We demonstrated that
saringosterol dose dependently inhibited adipocyte differentiation and expression of adipogenic marker genes such as adipocyte
fatty acid-binding protein,
adiponectin,
resistin, and
fatty acid synthase in 3T3-L1 cells. In addition,
saringosterol significantly inhibited the
mRNA and
protein expression of
peroxisome proliferator-activated receptor γ and
CCAAT enhancer-binding protein α in 3T3-L1 cells. Collectively, these findings indicate that
saringosterol isolated from S. muticum exhibits anti-
obesity effect by inhibiting the expression of adipogenic
transcription factors and marker genes and that it may be developed as a
drug to suppress adipogenesis. Copyright © 2017 John Wiley & Sons, Ltd.