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苹果多酚对 GSTT2 基因表达的影响,以及对 LT97 人结肠腺瘤细胞的 DNA 保护和增殖调节作用。

Impact of apple polyphenols on GSTT2 gene expression, subsequent protection of DNA and modulation of proliferation using LT97 human colon adenoma cells.

机构信息

Institute for Nutrition, Department of Nutritional Toxicology, Friedrich-Schiller-University Jena, Jena, Germany.

出版信息

Mol Nutr Food Res. 2009 Oct;53(10):1254-62. doi: 10.1002/mnfr.200800444.

Abstract

Apple extract (AE) enhances expression of glutathione S-transferases (e.g., GSTT2) in human colon cells (LT97). Therefore, aim of the present study was to identify functional consequences of GSTT2 induction by AE and to determine the relation of AE effects to isolated compounds. Polyphenol composition of AE was analyzed. LT97 cells were treated with AE or synthetic polyphenol mixture (SPM) under conditions that induced GSTT2, and challenged with GSTT2-2 substrate cumene hydroperoxide (CumOOH) to determine DNA damage using comet assay. Modulation of GSTT2 expression (real-time PCR) was reassessed, and the influence on cell proliferation and pro-oxidative potential of AE and SPM were assessed to understand additional mechanisms. Induction of GSTT2 by AE was accompanied by protection of LT97 cells from CumOOH-induced genotoxicity. Although SPM was unable to reflect AE-specific bioactivity related to GSTT2 modulation and anti-genotoxicity, inhibition of LT97 cell proliferation by SPM was comparable. Storage of AE caused changes in phenolic composition along with loss of activity regarding GSTT2 induction and amplified growth inhibition. At the applied concentrations, no H(2)O(2) formation was detectable with any of the substances. AE can protect against oxidatively induced DNA damage. Nevertheless, chemopreventive effects of AE strongly depend on the specific composition, which is modified by storage.

摘要

苹果提取物(AE)增强了人结肠细胞(LT97)谷胱甘肽 S-转移酶(例如 GSTT2)的表达。因此,本研究的目的是确定 AE 诱导 GSTT2 的功能后果,并确定 AE 效应与分离化合物之间的关系。分析了 AE 的多酚成分。在诱导 GSTT2 的条件下,用 AE 或合成多酚混合物(SPM)处理 LT97 细胞,并使用彗星试验用 GSTT2-2 底物 cumene hydroperoxide(CumOOH)挑战,以确定 DNA 损伤。重新评估 GSTT2 表达的调节,并评估 AE 和 SPM 对细胞增殖和促氧化潜能的影响,以了解其他机制。AE 诱导 GSTT2 的同时,保护 LT97 细胞免受 CumOOH 诱导的遗传毒性。尽管 SPM 无法反映与 GSTT2 调节和抗遗传毒性相关的 AE 特异性生物活性,但 SPM 抑制 LT97 细胞增殖的作用相当。AE 的储存导致酚类成分发生变化,同时丧失了 GSTT2 诱导和放大生长抑制的活性。在所应用的浓度下,任何物质都没有检测到 H2O2 的形成。AE 可以防止氧化诱导的 DNA 损伤。然而,AE 的化学预防作用强烈依赖于特定的组成,其通过储存而改变。

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