Effect of Anthocyanin Fractions from Selected Cultivars of Georgia-Grown Blueberries on Apoptosis and Phase II Enzymes

花青素 哌替尼丁 飞燕草素 马维定 氰化物 芍药苷 细胞凋亡 栽培 DNA断裂 化学 生物化学 抗氧化剂 天竺葵苷 谷胱甘肽还原酶 食品科学 谷胱甘肽 生物 园艺 程序性细胞死亡 谷胱甘肽过氧化物酶
作者
Anita Srivastava,Casimir C. Akoh,Joan G. Fischer,Gerard Krewer
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:55 (8): 3180-3185 被引量:116
标识
DOI:10.1021/jf062915o
摘要

In recent years, considerable attention has been paid to anthocyanins due to their abilities to inhibit oxidative stress and cell proliferation. The regulations of apoptosis and the phase II enzymes glutathione-S-transferase (GST) and quinone reductase (QR) are other potential mechanisms through which flavonoids such as anthocyanins may prevent cancer. Our study confirmed that anthocyanin fractions from high bush blueberry cultivars increased apoptosis using two different methods: DNA fragmentation and caspase-3 activity. The effect of anthocyanins on the activity of the detoxifying enzymes GST and QR was also determined. Major anthocyanins identified were delphinidin, cyanidin, peonidin, petunidin, and malvidin. In Tifblue and Powderblue cultivars, DNA fragmentation increased at anthocyanin concentrations from 50 to 150 μg/mL, but cells treated with the anthocyanin fraction of Brightblue and Brightwell showed a prominent ladder at 50−100 μg/mL when compared to cells treated with 150 μg/mL. There was a significant difference in the caspase-3 activity (P < 0.05) between the control cells and the cells treated with anthocyanins from all of the cultivars. The response correlated positively with dose. The QR activity was lower in all cells treated with an anthocyanin fraction from Tifblue, Powderblue, Brightblue, and Brightwell cultivars than in control cells (P < 0.05). The activity decreased gradually when treated with increased concentrations of anthocyanin fractions (50−150 μg/mL) in the Tifblue and Powderblue cultivars. The GST activity was lower (P < 0.05) in cells treated with anthocyanin fractions from all of the cultivars and at all concentrations. These results indicated that apoptosis was confirmed in HT-29 cells when treated with anthocyanins from blueberry cultivars at 50−150 μg/mL concentrations, but these same concentrations decrease QR and GST activities rather than induce them. Keywords: Anthocyanins; blueberries; caspase-3; cultivars; DNA fragmentation; DNA ladder; glutathione-S-transferase; phase-II enzymes; quinone reductase
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