College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 151-742, Korea.
Free Radic Biol Med. 2012 Sep 1;53(5):1198-208. doi: 10.1016/j.freeradbiomed.2012.06.039. Epub 2012 Jul 6.
Polyphenols have antioxidant effects. In view of the diverse biological activities of prenylated natural products, this study investigated whether polyphenols with prenyl residues have improved antioxidant and cytoprotective activity against oxidative stress, and explored the underlying basis for this effect. A set of structurally related polyphenols exhibited varying degrees of antioxidant effect in HepG2 cells, as evidenced by increases in cell viability against oxidative injury; kazinol E and C with three prenyls had greater potency than other kazinols having fewer prenyl chains. Polyphenols without prenyl (tupichinol C and resveratrol) showed weaker potency. Treatment with kazinol E diminished H(2)O(2) production and enabled cells to protect the mitochondria, as indicated by the inhibition of mitochondrial fragmentation, mitochondrial permeability transition, and cytochrome c release. Moreover, kazinol E activated LKB1 by its phosphorylation and cytoplasmic translocation, contributing to the protection of mitochondria via AMPK. In vitro or in a cell-based assay, tyrosine phosphorylation of Fyn was prohibited by kazinol E, which led to LKB1 activation, as shown by the experiments using Fyn over-expression construct or siRNA. SU6656, a known Fyn inhibitor, had a similar effect. Moreover, oxidative stress facilitated Fyn phosphorylation with repression of AMPKα and GSK3β phosphorylation, which was abolished by kazinol E treatment. The role of Fyn inhibition by kazinol E in AMPK-mediated protection of the cell viability and mitochondrial function was strengthened by ectopically expressed Fyn's reversal of these effects. In conclusion, kazinols as multi-prenylated polyphenols possess increased antioxidant and cytoprotective activity, which depends on the activation of LKB1-AMPK pathway downstream of Fyn inhibition.
多酚具有抗氧化作用。鉴于天然产物的类异戊二烯基化产物具有多种多样的生物活性,本研究探讨了具有类异戊二烯基残基的多酚是否具有改善的抗氧化和细胞保护活性,以抵抗氧化应激,并探索了这种作用的基础。一组结构相关的多酚在 HepG2 细胞中表现出不同程度的抗氧化作用,这表现在增加了细胞活力,以抵抗氧化损伤;具有三个类异戊二烯基的卡醇 E 和 C 比具有较少类异戊二烯基链的其他卡醇具有更高的效力。没有类异戊二烯基的多酚(tupichinol C 和白藜芦醇)表现出较弱的效力。卡醇 E 的处理减少了 H2O2 的产生,并使细胞能够保护线粒体,这表现在抑制线粒体片段化、线粒体通透性转换和细胞色素 c 释放。此外,卡醇 E 通过其磷酸化和细胞质易位激活 LKB1,通过 AMPK 促进线粒体的保护。在体外或基于细胞的测定中,卡醇 E 抑制了 Fyn 的酪氨酸磷酸化,从而导致 LKB1 的激活,这通过使用 Fyn 过表达构建体或 siRNA 的实验得到证明。SU6656,一种已知的 Fyn 抑制剂,具有类似的作用。此外,氧化应激通过抑制 AMPKα 和 GSK3β 的磷酸化来促进 Fyn 的磷酸化,而卡醇 E 的处理则消除了这种作用。卡醇 E 通过抑制 Fyn 对 AMPK 介导的细胞活力和线粒体功能保护的作用,通过外源性表达 Fyn 逆转这些作用得到了加强。总之,作为多类异戊二烯基化多酚的卡醇具有增加的抗氧化和细胞保护活性,这取决于 Fyn 抑制下游的 LKB1-AMPK 途径的激活。