論文

査読有り
2016年10月

Two Alkaloids from Bulbs of Lycoris sanguinea M-AXIM. Suppress PEPCK Expression by Inhibiting the Phosphorylation of CREB

PHYTOTHERAPY RESEARCH
  • Young Sook Yun
  • ,
  • Miki Tajima
  • ,
  • Shigeru Takahashi
  • ,
  • Yuji Takahashi
  • ,
  • Mariko Umemura
  • ,
  • Haruo Nakano
  • ,
  • Hyun Sun Park
  • ,
  • Hideshi Inoue

30
10
開始ページ
1689
終了ページ
1695
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1002/ptr.5676
出版者・発行元
WILEY-BLACKWELL

In the fasting state, gluconeogenesis is upregulated by glucagon. Glucagon stimulates cyclic adenosine monophosphate production, which induces the expression of key enzymes for gluconeogenesis, such as cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C), which are involved in gluconeogenesis through the protein kinase A/cAMP response element-binding protein (CREB) pathway. Using a luciferase reporter gene assay, a methanol extract of the bulbs of Lycoris sanguinea M-AXIM. var. kiushiana Makino was found to suppress cAMP-enhanced PEPCK-C promoter activity. In addition, two alkaloids, lycoricidine and lycoricidinol, in the extract were identified as active constituents. In forskolin-stimulated human hepatoma cells, these alkaloids suppressed the expression of a reporter gene under the control of cAMP response element and also prevented increases in the endogenous levels of phosphorylated CREB and PEPCK mRNA expression. These results suggest that lycoricidine and lycoricidinol suppress PEPCK-C expression by inhibiting the phosphorylation of CREB and may thus have the potential to prevent excessive gluconeogenesis in type 2 diabetes. Copyright (c) 2016 John Wiley & Sons, Ltd.

リンク情報
DOI
https://doi.org/10.1002/ptr.5676
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/27388056
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000385700400015&DestApp=WOS_CPL
ID情報
  • DOI : 10.1002/ptr.5676
  • ISSN : 0951-418X
  • eISSN : 1099-1573
  • PubMed ID : 27388056
  • Web of Science ID : WOS:000385700400015

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