TY - JOUR
T1 - Anti-obesity effects of boussingaulti gracilis miers var. pseudobaselloides bailey via activation of AMP-activated protein kinase in 3T3-L1 cells
AU - Kim, Hana
AU - Choung, Se Young
PY - 2012/9/1
Y1 - 2012/9/1
N2 - In a previous study, we demonstrated the anti-obesity and hypolipidemic effects of Boussingaulti gracilis Miers var. pseudobaselloides Bailey in high-fat diet-induced obese rats. The present study investigated the molecular mechanisms by which B. gracilis Miers var. pseudobaselloides Bailey ethanol extract (BGE) conferred antidifferentiation and anti-adipogenic effects in the 3T3-L1 preadipocyte differentiation model. BGE treatment significantly and dose-dependently suppressed lipid accumulation and down-regulated the expression of major transcription factors involved in adipogenesis, such as peroxisome proliferator-activated receptor-γ, CCAAT/enhancer binding protein α, sterol regulatory element-binding proteins, and their target genes. It is important that treatment with BGE increased phosphorylation of AMP-activated protein kinase (AMPK), which is one of the rate-limiting enzymes in the fatty acid synthesis pathway, and its direct downstream protein, acetyl-coenzyme A carboxylase. These results suggest that BGE may exert anti-adipogenic effects through regulation of AMPK activity and expression of genes involved in lipogenesis.
AB - In a previous study, we demonstrated the anti-obesity and hypolipidemic effects of Boussingaulti gracilis Miers var. pseudobaselloides Bailey in high-fat diet-induced obese rats. The present study investigated the molecular mechanisms by which B. gracilis Miers var. pseudobaselloides Bailey ethanol extract (BGE) conferred antidifferentiation and anti-adipogenic effects in the 3T3-L1 preadipocyte differentiation model. BGE treatment significantly and dose-dependently suppressed lipid accumulation and down-regulated the expression of major transcription factors involved in adipogenesis, such as peroxisome proliferator-activated receptor-γ, CCAAT/enhancer binding protein α, sterol regulatory element-binding proteins, and their target genes. It is important that treatment with BGE increased phosphorylation of AMP-activated protein kinase (AMPK), which is one of the rate-limiting enzymes in the fatty acid synthesis pathway, and its direct downstream protein, acetyl-coenzyme A carboxylase. These results suggest that BGE may exert anti-adipogenic effects through regulation of AMPK activity and expression of genes involved in lipogenesis.
KW - AMP-activated protein kinase
KW - Boussingaulti gracilis Miers var. pseudobaselloides Bailey
KW - anti-obesity
KW - antilipogenesis
KW - β-oxidation
UR - http://www.scopus.com/inward/record.url?scp=84865679644&partnerID=8YFLogxK
U2 - 10.1089/jmf.2011.2126
DO - 10.1089/jmf.2011.2126
M3 - Article
C2 - 22871035
AN - SCOPUS:84865679644
SN - 1096-620X
VL - 15
SP - 811
EP - 817
JO - Journal of Medicinal Food
JF - Journal of Medicinal Food
IS - 9
ER -