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首页> 外文期刊>Apoptosis: An international journal on programmed cell death >Effect of xanthohumol and isoxanthohumol on 3T3-L1 cell apoptosis and adipogenesis
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Effect of xanthohumol and isoxanthohumol on 3T3-L1 cell apoptosis and adipogenesis

机译:黄腐酚和异黄腐酚对3T3-L1细胞凋亡和脂肪形成的影响

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摘要

Xanthohumol (XN), the chalcone from beer hops has several biological activities. XN has been shown to induce apoptosis in cancer cells and also has been reported to be involved in lipid metabolism. Based on these studies and our previous work with natural compounds, we hypothesized that XN and its isomeric flavanone, isoxanthohumol (IXN), would induce apoptosis in adipocytes through the mitochondrial pathway and would inhibit maturation of preadipocytes. Adipocytes were treated with various concentrations of XN or IXN. In mature adipocytes both XN and IXN decreased viability, increased apoptosis and increased ROS production, XN being more effective. Furthermore, the antioxidants ascorbic acid and 2-mercaptoethanol prevented XN and IXN-induced ROS generation and apoptosis. Immunoblotting analysis showed an increase in the levels of cytoplasmic cytochrome c and cleaved poly (ADP-ribose) polymerase (PARP) by XN and IXN. Concomitantly, we observed activation of the effectors caspase-3/7. In maturing preadipocytes both XN and IXN were effective in reducing lipid content, XN being more potent. Moreover, the major adipocyte marker proteins such as PPAR gamma, C/EBP alpha, and aP2 decreased after treatment with XN during the maturation period and that of DGAT1 decreased after treatment with XN and IXN. Taken together, our data indicate that both XN and IXN inhibit differentiation of preadipocytes, and induce apoptosis in mature adipocytes, but XN is more potent.
机译:Xanthohumol(XN),啤酒花中的查尔酮具有多种生物活性。 XN已显示可诱导癌细胞凋亡,也已报道其参与脂质代谢。基于这些研究以及我们之前对天然化合物的研究,我们假设XN及其异构体黄烷酮异黄腐酚(IXN)会通过线粒体途径诱导脂肪细胞凋亡,并抑制前脂肪细胞的成熟。用各种浓度的XN或IXN处理脂肪细胞。在成熟的脂肪细胞中,XN和IXN均降低了活力,增加了细胞凋亡并增加了ROS的产生,XN更有效。此外,抗氧化剂抗坏血酸和2-巯基乙醇可防止XN和IXN诱导的ROS生成和凋亡。免疫印迹分析表明,XN和IXN的细胞质细胞色素c和裂解的聚(ADP-核糖)聚合酶(PARP)水平增加。同时,我们观察到了效应子caspase-3 / 7的激活。在成熟的前脂肪细胞中,XN和IXN均可有效降低脂质含量,而XN则更有效。此外,在成熟期,用XN处理后,主要的脂肪细胞标记蛋白(如PPARγ,C / EBPα和aP2)下降,而用XN和IXN处理后,DGAT1的蛋白下降。两者合计,我们的数据表明XN和IXN都抑制前脂肪细胞的分化,并诱导成熟脂肪细胞的凋亡,但XN更有效。

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