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14-Deoxy-11,12-didehydroandrographolide suppresses adipogenesis of 3 T3-L1 preadipocytes by inhibiting CCAAT/enhancer-binding protein β activation and AMPK-mediated mitotic clonal expansion.

Authors :
Li, Chien-Chun
Yen, Chih-Ching
Fan, Ciou-Ting
Chuang, Wei-Ting
Huang, Chin-Shiu
Chen, Haw-Wen
Lii, Chong-Kuei
Source :
Toxicology & Applied Pharmacology. Nov2018, Vol. 359, p82-90. 9p.
Publication Year :
2018

Abstract

Abstract Obesity is highly correlated with several metabolic disorders. Adipocyte differentiation is a key process in determining obesogenesis. 14-Deoxy-11,12-didehydroandrographolide (deAND) is a diterpenoid rich in Andrographis paniculata (Burm.f.) Nees., a herbal medicine commonly used to treat colds, infections, and liver diseases. We investigated whether deAND inhibits the adipogenesis of 3T3-L1 cells and the underlying mechanisms. We found that deAND (0–15 μM) dose-dependently inhibits the mRNA and protein expression of peroxisome proliferator-activated receptor γ, sterol regulatory element-binding protein 1c, fatty acid synthase, and stearoyl-CoA desaturase-1. Cellular lipid accumulation was decreased by deAND, and the early phase of adipocyte differentiation was critical for this inhibition. Immunoblotting revealed that deAND attenuated differentiation medium–induced protein kinase A (PKA) and cAMP response element-binding protein (CREB) activation, which leads to down-regulating C/EBPβ transcription. Moreover, deAND inhibited ERK- and GSK3β-mediated C/EBPβ transcriptional activity. Flow cytometry analysis showed that deAND impaired the progression of mitotic clonal expansion (MCE) by arresting the cell cycle at the G0/G1 phase, while the expression of cyclin D1, cyclin E, CDK6, and CDK2 was attenuated. deAND increased the phosphorylation of AMPK and raptor, an mTOR-interacting partner, which inhibited the mTOR-driven phosphorylation of P70S6K and eukaryotic translation initiation factor 4E binding protein. In the presence of compound C, deAND modulation of AMPK-mTOR signaling and inhibition of cell cycle regulator expression were reversed. Our results reveal that the anti-adipogenic effect of deAND is likely through inhibition of the PKA-CREB-C/EBPβ and AMPK/mTOR pathways, which leads to down-regulating C/EBPβ-driven lipogenic protein expression and halting MCE progression. Graphical abstract Unlabelled Image Highlights • 14-Deoxy-11,12-didehydroandrographolide is a diterpenoid of Andrographis paniculata. • 14-Deoxy-11,12-didehydroandrographolide can suppress adipogenesis in preadipocytes. • 14-Deoxy-11,12-didehydroandrographolide attenuates PKA-CREB-C/EBPβ activation. • 14-Deoxy-11,12-didehydroandrographolide leads to halted mitotic clonal expansion. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0041008X
Volume :
359
Database :
Academic Search Index
Journal :
Toxicology & Applied Pharmacology
Publication Type :
Academic Journal
Accession number :
132319004
Full Text :
https://doi.org/10.1016/j.taap.2018.09.028