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啤酒花黄素与厚朴酚联用对3T3-L1脂肪细胞凋亡的增强作用。

Enhanced effects of xanthohumol plus honokiol on apoptosis in 3T3-L1 adipocytes.

作者信息

Yang Jeong-Yeh, Della-Fera Mary Anne, Rayalam Srujana, Baile Clifton A

机构信息

Department of Animal and Dairy Science, University of Georgia, Athens, Georgia, USA.

出版信息

Obesity (Silver Spring). 2008 Jun;16(6):1232-8. doi: 10.1038/oby.2008.66. Epub 2008 Mar 27.

Abstract

OBJECTIVE

To study the effects of xanthohumol (XN), a flavonoid found in hops (Humulus lupulus) and honokiol (HK), a lignan isolated from Magnolia officinalis, alone and in combination, on apoptotic signaling in 3T3-L1 adipocytes.

METHODS AND PROCEDURES

3T3-L1 mature adipocytes were incubated with various concentrations of XN and HK alone and in combination. Viability and apoptosis were quantified using an MTS-based cell viability assay and single-stranded DNA assay, respectively. Expression of apoptosis related proteins including cleaved poly(ADP-ribose) polymerase (PARP), cytochrome c, Bcl-2, caspase-3/7, phosphatase and tensin homolog deleted on chromosome 10 (PTEN) and Akt was analyzed by western blotting.

RESULTS

Combinations of XN and HK significantly decreased viability and induced apoptosis in a dose-dependent manner and more than the additive responses to XN and HK alone. Western blot analysis showed an increase in cleaved PARP and cytochrome c release and decrease in expression of Bcl-2 protein by XN plus HK, whereas XN and HK individually had no effect. Furthermore, the combination of XN and HK activated PTEN and inactivated Akt by decreasing levels of phosphorylated PTEN and phosphorylated Akt.

DISCUSSION

We demonstrated that although XN and HK showed little or no effect as individual compounds, in combination (XN plus HK) they showed enhanced activity in inducing apoptosis via the cytochrome c/caspase-3/PARP and PTEN/Akt pathways in 3T3-L1 adipocytes.

摘要

目的

研究啤酒花(Humulus lupulus)中发现的类黄酮黄腐酚(XN)和从厚朴(Magnolia officinalis)中分离出的木脂素厚朴酚(HK)单独及联合使用对3T3-L1脂肪细胞凋亡信号传导的影响。

方法和步骤

将3T3-L1成熟脂肪细胞分别与不同浓度的XN和HK单独及联合孵育。分别使用基于MTS的细胞活力测定法和单链DNA测定法对细胞活力和凋亡进行定量。通过蛋白质免疫印迹法分析凋亡相关蛋白的表达,包括裂解的聚(ADP-核糖)聚合酶(PARP)、细胞色素c、Bcl-2、半胱天冬酶-3/7、第10号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)以及Akt。

结果

XN和HK联合使用显著降低细胞活力并以剂量依赖性方式诱导凋亡,且比单独使用XN和HK的相加反应更明显。蛋白质免疫印迹分析显示,XN加HK可使裂解的PARP增加、细胞色素c释放,并使Bcl-2蛋白表达降低,而XN和HK单独使用则无此作用。此外,XN和HK联合使用可激活PTEN并使Akt失活,方法是降低磷酸化PTEN和磷酸化Akt的水平。

讨论

我们证明,尽管XN和HK作为单一化合物时作用很小或无作用,但联合使用(XN加HK)时,它们通过细胞色素c/半胱天冬酶-3/PARP和PTEN/Akt途径在3T3-L1脂肪细胞中诱导凋亡的活性增强。

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