咖啡酸、鞣花酸和阿魏酸在正常人外周血单个核细胞中的抗凋亡活性:一种不依赖Bcl-2的机制。

Anti-apoptotic activity of caffeic acid, ellagic acid and ferulic acid in normal human peripheral blood mononuclear cells: a Bcl-2 independent mechanism.

作者信息

Khanduja Krishan Lal, Avti Pramod Kumar, Kumar Surender, Mittal Nidhi, Sohi Kiranjit Kaur, Pathak Chander Mohan

机构信息

Department of Biophysics, Postgraduate Institute of Medical Education and Research, Chandigarh-160012, India.

出版信息

Biochim Biophys Acta. 2006 Feb;1760(2):283-9. doi: 10.1016/j.bbagen.2005.12.017. Epub 2006 Jan 17.

Abstract

Polyphenols have been shown to induce apoptosis in a variety of tumor cells including leukemia both in vitro and in vivo. However, their action on normal human peripheral blood mononuclear cells (PBMCs) during oxidative stress remains to be explored. In this study, we have evaluated the anti-apoptotic and radical scavenging activities of dietary phenolics, namely caffeic acid (CA), ellagic acid (EA) and ferulic acid (FA). H2O2-induced apoptosis in normal human PBMCs was assayed by phosphotidylserine externalization, nucleosomal damage and DNA fragmentation. Incubation of PBMCs with 5 mM H2O2 led to increased Annexin-V binding to externalized phosphatidyl serine (PS), an event of pre-apoptotic stage of the cell. Peripheral blood mononuclear cells pretreated with phenolics could resist H2O2-induced apoptotic damage. Caffeic acid (60 and 120 microM) and EA (100 and 200 microM) caused no change in externalization of PS, whereas FA (100 and 200 microM) increased externalization of PS in PBMCs treated with H2O2. The effects of phenolics were abolished to a large extent by culturing the PBMCs for 24 h after washing the phenolics from the medium. Inhibitory activities of these phenolics on lipid peroxidation were in the order of EA<CA<FA. DPPH-scavenging activities of EA, CA and FA were found to be 31.2+/-1.36, 50+/-1.86 and 73.0+/-1.58 microM respectively. Although, the phenolics significantly inhibited DNA damage and lipid peroxidation, they could not alter the Bcl-2 expression in PBMCs. In conclusion, the anti-apoptotic effect of EA, CA and FA in PBMCs seems to be through the Bcl-2 independent mechanism.

摘要

多酚类物质已被证明在体外和体内均可诱导包括白血病细胞在内的多种肿瘤细胞凋亡。然而,它们在氧化应激期间对正常人外周血单核细胞(PBMC)的作用仍有待探索。在本研究中,我们评估了膳食酚类物质,即咖啡酸(CA)、鞣花酸(EA)和阿魏酸(FA)的抗凋亡和自由基清除活性。通过磷脂酰丝氨酸外化、核小体损伤和DNA片段化检测H2O2诱导的正常人PBMC凋亡。用5 mM H2O2孵育PBMC导致膜联蛋白-V与外化的磷脂酰丝氨酸(PS)结合增加,这是细胞凋亡前期的一个事件。用酚类物质预处理的外周血单核细胞可抵抗H2O2诱导的凋亡损伤。咖啡酸(60和120 microM)和EA(100和200 microM)对PS外化无影响,而FA(100和200 microM)增加了H2O2处理的PBMC中PS的外化。从培养基中洗去酚类物质后,将PBMC培养24小时,酚类物质的作用在很大程度上被消除。这些酚类物质对脂质过氧化的抑制活性顺序为EA<CA<FA。发现EA、CA和FA的DPPH清除活性分别为31.2±1.36、50±1.86和73.0±1.58 microM。尽管酚类物质显著抑制DNA损伤和脂质过氧化,但它们不能改变PBMC中Bcl-2的表达。总之,EA、CA和FA在PBMC中的抗凋亡作用似乎是通过不依赖Bcl-2的机制实现的。

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