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槲皮素、染料木黄酮和山奈酚对3T3-L1前脂肪细胞中谷胱甘肽及谷胱甘肽-氧化还原循环酶的影响。

Effect of quercetin, genistein and kaempferol on glutathione and glutathione-redox cycle enzymes in 3T3-L1 preadipocytes.

作者信息

Boadi William Y, Amartey Paul K, Lo Andrew

机构信息

a Department of Chemistry , Tennessee State University , Nashville , TN , USA.

出版信息

Drug Chem Toxicol. 2016;39(3):239-47. doi: 10.3109/01480545.2015.1082135. Epub 2015 Sep 7.

DOI:10.3109/01480545.2015.1082135
PMID:27063963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6042231/
Abstract

CONTEXT AND OBJECTIVE

Many studies have shown that cellular redox potential is largely determined by glutathione (GSH), which accounts for more than 90% of cellular nonprotein thiols. The aim of this study was to delineate the effect of three flavonoids - namely, quercetin, kaempferol and genistein - and exogenous GSH on oxidative damage by the Fenton's pathway through the GSH and GSH-redox cycle enzymes in 3T3-L1 cells.

MATERIALS AND METHODS

3T3-L1 preadipocytes were exposed to each flavonoid and GSH at concentrations of 0, 5, 10, 15, 20 and 25 µM and then GSH levels and activities of glutathione peroxidase (GSH-Px), glutathione reductase (GSH-Rx) and superoxide dismutase (SOD) were measured.

RESULTS

Exogenous GSH did not have significant effect on intracellular GSH although slight decrease was observed at 15-25 µM doses. However, each of the three flavonoids sustained intracellular GSH levels in the cells as compared to the respective controls. Quercetin had the most profound effect, followed by kaempferol and genistein in that order. GSH-Px, GSH-Rx and SOD activities increased for all the doses tested compared to their respective controls. Again, quercetin had the maximum increase in enzyme activities followed by kaempferol and genistein for the enzymes tested.

DISCUSSION AND CONCLUSION

These findings suggest that the flavonoids play an important role in diminishing oxidation-induced biochemical damages. The enhancement of these enzymes may increase the resistance of the organism against oxidative damage by the Fenton's pathway.

摘要

背景与目的

许多研究表明,细胞氧化还原电位很大程度上由谷胱甘肽(GSH)决定,它占细胞非蛋白硫醇的90%以上。本研究的目的是通过3T3-L1细胞中的谷胱甘肽和谷胱甘肽氧化还原循环酶,描述三种黄酮类化合物(即槲皮素、山奈酚和染料木黄酮)以及外源性谷胱甘肽对芬顿途径氧化损伤的影响。

材料与方法

将3T3-L1前脂肪细胞暴露于浓度为0、5、10、15、20和25 μM的每种黄酮类化合物和谷胱甘肽中,然后测量谷胱甘肽水平以及谷胱甘肽过氧化物酶(GSH-Px)、谷胱甘肽还原酶(GSH-Rx)和超氧化物歧化酶(SOD)的活性。

结果

外源性谷胱甘肽对细胞内谷胱甘肽没有显著影响,尽管在15 - 25 μM剂量下观察到轻微下降。然而,与各自的对照组相比,三种黄酮类化合物中的每一种都能维持细胞内谷胱甘肽水平。槲皮素的影响最为显著,其次是山奈酚和染料木黄酮,顺序依次如此。与各自的对照组相比,所有测试剂量下GSH-Px、GSH-Rx和SOD的活性均增加。同样,对于所测试的酶,槲皮素的酶活性增加最大,其次是山奈酚和染料木黄酮。

讨论与结论

这些发现表明,黄酮类化合物在减少氧化诱导的生化损伤方面发挥着重要作用。这些酶的增强可能会增加生物体对芬顿途径氧化损伤的抵抗力。

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