Usui Shigeyuki, Soda Midori, Iguchi Kazuhiro, Abe Naohito, Oyama Masayoshi, Nakayama Tatsushi, Kitaichi Kiyoyuki
Department of Biomedical Pharmaceutics Gifu Pharmaceutical University Gifu Japan.
Instrumental Analysis Center Gifu Pharmaceutical University Gifu Japan.
Food Sci Nutr. 2019 Oct 21;7(11):3819-3826. doi: 10.1002/fsn3.1246. eCollection 2019 Nov.
10-Hydroxy--2-decenoic acid (10H2DA) is a unique lipid component of royal jelly produced by worker honeybees that exerts insulin-like effects. We herein investigated the effects of 10H2DA on the gene expression of aquaporin 9 (AQP9), which functions as a glycerol transporter in the liver, to clarify whether 10H2DA modulates energy metabolism. 10H2DA suppressed AQP9 gene expression in HepG2 cells by promoting the phosphorylation of Akt and AMP-activated protein kinase (AMPK). This suppression was partially recovered by the treatment of cells with inhibitors for Akt and AMPK. Based on the result showing that leptomycin B partially recovered the suppression of AQP9 gene expression, 10H2DA inhibited the expression of Foxa2, a transcription factor for the AQP9 gene, and also induced its nuclear exclusion. Although 10H2DA up-regulated phosphoenolpyruvate carboxykinase and glucose-6-phosphatase gene expression, this was suppressed through the modulation of Foxa2 by insulin. These results suggest that 10H2DA suppresses AQP9 gene expression through the phosphorylation of Akt and AMPK and down-regulation of Foxa2 expression.
10-羟基-2-癸烯酸(10H2DA)是工蜂分泌的蜂王浆中一种独特的脂质成分,具有胰岛素样作用。我们在此研究了10H2DA对水通道蛋白9(AQP9)基因表达的影响,AQP9在肝脏中作为甘油转运体发挥作用,以阐明10H2DA是否调节能量代谢。10H2DA通过促进Akt和AMP激活的蛋白激酶(AMPK)的磷酸化来抑制HepG2细胞中AQP9基因的表达。用Akt和AMPK抑制剂处理细胞可部分恢复这种抑制作用。基于雷帕霉素B部分恢复AQP9基因表达抑制的结果,10H2DA抑制了AQP9基因的转录因子Foxa2的表达,并诱导其核输出。尽管10H2DA上调了磷酸烯醇式丙酮酸羧激酶和葡萄糖-6-磷酸酶基因的表达,但这通过胰岛素对Foxa2的调节而受到抑制。这些结果表明,10H2DA通过Akt和AMPK的磷酸化以及Foxa2表达的下调来抑制AQP9基因的表达。