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大豆皂苷在Hepa1c1c7小鼠肝癌细胞中的抗氧化及醌还原酶活性

Antioxidant and Quinone Reductase Activity of Soyasaponins in Hepa1c1c7 Mouse Hepatocarcinoma Cells.

作者信息

Hwang Eun-Sun

机构信息

Department of Nutrition and Culinary Science and Korean Foods Global Center, Hankyong National University, Gyeonggi 17579, Korea.

出版信息

Prev Nutr Food Sci. 2017 Dec;22(4):300-305. doi: 10.3746/pnf.2017.22.4.300. Epub 2017 Dec 31.

Abstract

Saponins have been reported to possess several health beneficial activities including hypocholesterolemic, immune-stimulatory, and anticarcinogenic. The objectives of this study were to determine if soysaponins are radical scavengers and inducers of quinone reductase (QR) activity in Hepa1c1c7 murine hepatoma cell line. The antioxidant capacity of soyasaponin was evaluated using the 1,1'-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radical scavenging methods. Soyasaponin showed 75.7% radical scavenging activity in the DPPH assay and 81.4% in the ABTS method at 100 μg/mL concentration. Cellular proliferation was determined using the methylthiazolyldiphenyl-tetrazolium bromide colorimetric assay. Soyasaponin inhibited cell growth in a dose-dependent (0.1~100 μg/mL) manner, and growth inhibition was 30% and 39% at 100 μg/mL of saponin after 24 h and 48 h incubation, respectively. Soyasaponin showed QR induction in a dose-dependent manner. Ten, 50, and 100 μg/mL of soyasaponin resulted in a 1.6-, 2.2-, and 2.9-fold induction of QR, respectively. These results provide a basis for the potential of soysaponin as a chemopreventive agent.

摘要

据报道,皂苷具有多种有益健康的活性,包括降胆固醇、免疫刺激和抗癌作用。本研究的目的是确定大豆皂苷是否为Hepa1c1c7小鼠肝癌细胞系中的自由基清除剂和醌还原酶(QR)活性诱导剂。使用1,1'-二苯基-2-苦基肼(DPPH)和2,2'-联氮-双-(3-乙基苯并噻唑啉-6-磺酸)(ABTS)自由基清除方法评估大豆皂苷的抗氧化能力。在100μg/mL浓度下,大豆皂苷在DPPH试验中显示出75.7%的自由基清除活性,在ABTS方法中显示出81.4%的自由基清除活性。使用甲基噻唑基二苯基溴化四氮唑比色法测定细胞增殖。大豆皂苷以剂量依赖性(0.1~100μg/mL)方式抑制细胞生长,在100μg/mL皂苷浓度下孵育24小时和48小时后,生长抑制率分别为30%和39%。大豆皂苷以剂量依赖性方式显示出QR诱导作用。10、50和100μg/mL的大豆皂苷分别导致QR诱导1.6倍、2.2倍和2.9倍。这些结果为大豆皂苷作为化学预防剂的潜力提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3b1/5758093/96b7ed7c99c8/pnfs-22-300f1.jpg

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