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蜂胶的降血糖作用:通过抑制 HepG2 细胞中 GSK-3α/β 的 Y279 和 Y216 自身磷酸化来降低葡萄糖-6-磷酸酶的表达。

Antidiabetic effect of propolis: reduction of expression of glucose-6-phosphatase through inhibition of Y279 and Y216 autophosphorylation of GSK-3α/β in HepG2 cells.

机构信息

Department of Biotechnology, Bio-Energy Research Center, Biotechnology Research Institute, Chonnam National University, 300 Yongbong-Dong, Buk-Gu, Gwangju 500-757, Korea.

出版信息

Phytother Res. 2010 Oct;24(10):1554-61. doi: 10.1002/ptr.3147.

DOI:10.1002/ptr.3147
PMID:20878710
Abstract

Propolis is a sticky, resinous material that honey bees collect from various plants, and mix with wax and other secretions. The aim of this study was to evaluate the antidiabetic effect of propolis through an analysis of the expression and enzyme activity of glucose-6-phosphatase (G6Pase) and to elucidate the mechanism by which propolis inhibits G6Pase gene expression. When HepG2 cells were incubated in high glucose media (25 mm), G6Pase expression was induced. Propolis significantly reduced the expression and enzyme activity of G6Pase; however, the hypoglycemic effect was not abolished by the phosphoinositide 3-kinase inhibitor, LY294002, and by the mitogen-activated protein kinase (MAPK) inhibitor, U0126. Propolis inhibited the activity of GSK3α and β via the inhibition of serine and tyrosine phosphorylation, specifically, Y279 for GSK3α and Y216 for GSK3β. The phosphorylations of Y279 and Y216 occur through autophosphorylation by GSK3α/β and are involved in their own activity. Although propolis showed antioxidant activity, antidiabetic effect of propolis was not influenced by hydrogen peroxide and N-acetylcysteine. These results suggest that propolis inhibits the expression of G6Pase by inhibiting the autophosphorylation of Y279 and Y216 of GSK3α and β, respectively, which are involved in the activation of GSK3. These findings suggest that propolis may be a potential antidiabetic agent for the treatment of insulin-insensitive diabetes.

摘要

蜂胶是一种粘性树脂状物质,由蜜蜂从各种植物中采集,并与蜂蜡和其他分泌物混合而成。本研究旨在通过分析葡萄糖-6-磷酸酶(G6Pase)的表达和酶活性来评估蜂胶的抗糖尿病作用,并阐明蜂胶抑制 G6Pase 基因表达的机制。当 HepG2 细胞在高葡萄糖培养基(25mm)中孵育时,G6Pase 的表达被诱导。蜂胶显著降低了 G6Pase 的表达和酶活性;然而,磷酸肌醇 3-激酶抑制剂 LY294002 和丝裂原活化蛋白激酶(MAPK)抑制剂 U0126 并没有消除其降血糖作用。蜂胶通过抑制丝氨酸和酪氨酸磷酸化抑制 GSK3α 和β的活性,具体来说,GSK3α 的 Y279 和 GSK3β 的 Y216。Y279 和 Y216 的磷酸化通过 GSK3α/β 的自身磷酸化发生,并参与其自身的活性。尽管蜂胶具有抗氧化活性,但蜂胶的抗糖尿病作用不受过氧化氢和 N-乙酰半胱氨酸的影响。这些结果表明,蜂胶通过抑制 GSK3α 和β 的 Y279 和 Y216 的自身磷酸化来抑制 G6Pase 的表达,这涉及 GSK3 的激活。这些发现表明,蜂胶可能是治疗胰岛素不敏感型糖尿病的潜在抗糖尿病药物。

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