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水果和蔬菜提取物可激活IMR-32细胞中的抗氧化反应元件。

Extracts of Fruits and Vegetables Activate the Antioxidant Response Element in IMR-32 Cells.

作者信息

Orena Stephen, Owen Jennifer, Jin Fuxia, Fabian Morgan, Gillitt Nicholas D, Zeisel Steven H

机构信息

University of North Carolina at Chapel Hill Nutrition Research Institute, Kannapolis, NC;

Dole Nutrition Research Laboratory, Kannapolis, NC; and.

出版信息

J Nutr. 2015 Sep;145(9):2006-11. doi: 10.3945/jn.115.216705. Epub 2015 Jul 29.

Abstract

BACKGROUND

The biological effects of antioxidant nutrients are mediated in part by activation of antioxidant response elements (AREs) on genes for enzymes involved in endogenous pathways that prevent free radical damage. Traditional approaches for identifying antioxidant molecules in foods, such as total phenolic compound (TP) content or oxygen radical absorption capacity (ORAC), do not measure capacity to activate AREs.

OBJECTIVES

The goal of this study was to develop an assay to assess the ARE activation capacity of fruit and vegetable extracts and determine whether such capacity was predicted by TP content and/or ORAC activity.

METHODS

Fruits and vegetables were homogenized, extracted with acidified ethanol, lyophilized, and resuspended in growth medium. Human IMR-32 neuroblastoma cells, transfected with an ARE-firefly luciferase reporter, were exposed to extracts for 5 h. Firefly luciferase was normalized to constitutively expressed Renilla luciferase with tertiary butylhydroquinone (tBHQ) as a positive control. TP content and ORAC activity were measured for each extract. Relations between TPs and ORAC and ARE activity were determined.

RESULTS

A total of 107 of 134 extracts tested significantly activated the ARE-luciferase reporter from 1.2- to 58-fold above that of the solvent control (P < 0.05) in human IMR-32 cells. ARE activity, TP content, and ORAC ranked higher in peels than in associated flesh. Despite this relation, ARE activity did not correlate with TP content (Spearman ρ = 0.05, P = 0.57) and only modestly but negatively correlated with ORAC (Spearman ρ = -0.24, P < 0.01). Many extracts activated the ARE more than predicted by the TP content or ORAC.

CONCLUSIONS

The ARE reporter assay identified many active fruit and vegetable extracts in human IMR-32 cells. There are components of fruits and vegetables that activate the ARE but are not phenolic compounds and are low in ORAC. The ARE-luciferase reporter assay is likely a better predictor of the antioxidant benefits of fruits and vegetables than TP or ORAC.

摘要

背景

抗氧化营养素的生物学效应部分是通过激活抗氧化反应元件(ARE)来介导的,这些元件存在于参与防止自由基损伤的内源性途径的酶的基因上。传统的鉴定食物中抗氧化分子的方法,如总酚化合物(TP)含量或氧自由基吸收能力(ORAC),并不能测量激活ARE的能力。

目的

本研究的目的是开发一种检测方法,以评估水果和蔬菜提取物的ARE激活能力,并确定这种能力是否可以通过TP含量和/或ORAC活性来预测。

方法

将水果和蔬菜匀浆,用酸化乙醇提取,冻干,并重新悬浮于生长培养基中。将转染了ARE-萤火虫荧光素酶报告基因的人IMR-32神经母细胞瘤细胞暴露于提取物中5小时。以叔丁基对苯二酚(tBHQ)作为阳性对照,将萤火虫荧光素酶活性标准化为组成型表达的海肾荧光素酶活性。测量每种提取物的TP含量和ORAC活性。确定TP、ORAC与ARE活性之间的关系。

结果

在人IMR-32细胞中,134种测试提取物中的107种显著激活了ARE-荧光素酶报告基因,比溶剂对照高出1.2至58倍(P<0.05)。果皮中的ARE活性、TP含量和ORAC高于相应的果肉。尽管存在这种关系,但ARE活性与TP含量不相关(Spearman ρ=0.05,P=0.57),与ORAC仅呈适度的负相关(Spearman ρ=-0.24,P<0.01)。许多提取物对ARE的激活程度超过了TP含量或ORAC的预测值。

结论

ARE报告基因检测法鉴定出了许多在人IMR-32细胞中有活性的水果和蔬菜提取物。水果和蔬菜中存在一些能激活ARE但不是酚类化合物且ORAC值较低的成分。ARE-荧光素酶报告基因检测法可能比TP或ORAC更能预测水果和蔬菜的抗氧化益处。

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