1′-acetoxychavicol acetate inhibits adipogenesis in 3T3-L1 adipocytes and in high fat-fed rats

Rie Ohnishi, Isao Matsui-Yuasa, Yohei Deguchi, Keisuke Yaku, Masaki Tabuchi, Hiroshi Munakata, Yasumitsu Akahoshi, Akiko Kojima-Yuasa*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Alpinia galanga and Languas galanga, which are plants belonging to the ginger family, are frequently used for cooking, especially in Thai and Indonesian cuisine. The compound 1′-acetoxychavicol acetate (ACA), which is naturally obtained from the rhizomes and seeds of these gingers, has antioxidant and anti-inflammatory properties. We investigated the anti-obesity effects of ACA in 3T3-L1 adipocytes and in high fat diet (HFD)-induced rat models of obesity. ACA caused a significant decrease in the activity of GPDH in 3T3-L1 adipocytes without eliciting cell cytotoxicity, and it inhibited cellular lipid accumulation through the down-regulation of transcription factors such as PPARγ and C/EBP. ACA also induced a dose-dependent phosphorylation of AMP-activated protein kinase (AMPK). In the animal model, rats fed an HFD containing 0.05% ACA gained less weight than rats fed an HFD alone. The visceral fat mass in rats fed an HFD containing 0.05% ACA tended to be lower than that in rats fed an HFD alone. Furthermore, a histological examination of livers from rats fed an HFD showed steatohepatitis. However, rats fed an HFD containing 0.05% ACA showed no histopathological changes in the liver tissue. Our results show that ACA exerts anti-obesity activities both in vitro and in vivo and suggests that ACA may have a novel preventive activity against obesity and possibly other metabolic diseases.

Original languageEnglish
Pages (from-to)1189-1204
Number of pages16
JournalAmerican Journal of Chinese Medicine
Volume40
Issue number6
DOIs
StatePublished - 2012

Keywords

  • 1′-Acetoxychavicol Acetate
  • 3T3-L1 Cell
  • AMP-Activated Protein Kinase
  • GPDH
  • High-Fat Diet Fed Rat
  • PPARγ

ASJC Scopus subject areas

  • Complementary and alternative medicine

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