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Antioxidant and Apoptotic Activity of Papaya Peel Extracts in HepG2 Cells

机译:木瓜皮提取物对HepG2细胞的抗氧化和凋亡活性

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Papaya peels (PP) are discarded after consuming the fruit. However, they contain antioxidants. Oxidative damage caused by free radicals has major implications in many chronic diseases. The objective of this study was to determine in-vitro antioxidant and apoptotic activity of PP extracts. Modulation of endogenous glutathione (GSH), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), cyclo-oxygenase-2 (COX-2), caspase-3 activities and DNA fragmentation by PP extracts in HepG2 cells were evaluated. Gallic acid (18.06 μg/g), caffeic acid (29.28 μg/g), p-coumaric acid (38.16 μg/g), ferulic acid (95.46 μg/g) and quercetin (3.17 μg/g) were the major polyphenols quantified in PP extracts. In-vitro antioxidant capacity of PP was determined by ferric reducing antioxidant potential (31.86 μM Fe+2/g), trolox equivalent antioxidant capacity (14.56 mM trolox equivalents (TE)/g), oxygen radical scavenging activity (30.88 mM TE/g) and 2,2-diphenyl-1-picrylhydrazyl radical scavenging ability (IC50-8.33 mg/ml). Induction of oxidative stress significantly (p ≤ 0.05) lowered SOD, CAT, GPx, GR activities and GSH levels by 3.1, 1.46, 2.87, 1.34 and 1.32 folds compared to control respectively. However, treating cells with PP extracts significantly (p ≤ 0.05) enhanced SOD, CAT, GPx, GR activities and GSH compared to oxidative stress induced cells. Treating cells with PP extracts significantly (p ≤ 0.05) lowered COX-2 activity, enhanced caspase-3 activity and induced DNA fragmentation, indicating that PP extracts caused cell death by apoptosis. In conclusion, anti-cancer properties of PP extracts may be due to the synergistic effect of free radical scavenging ability, induction antioxidant enzymes and by inducing apoptosis.
机译:食用水果后将木瓜皮(PP)丢弃。但是,它们含有抗氧化剂。自由基引起的氧化损伤在许多慢性疾病中具有重要意义。这项研究的目的是确定PP提取物的体外抗氧化剂和凋亡活性。内源性谷胱甘肽(GSH),超氧化物歧化酶(SOD),过氧化氢酶(CAT),谷胱甘肽过氧化物酶(GPx),谷胱甘肽还原酶(GR),环加氧酶2(COX-2),胱天蛋白酶3活性和DNA片段的调节对HepG2细胞中的PP提取物进行了评估。没食子酸(18.06μg/ g),咖啡酸(29.28μg/ g),对香豆酸(38.16μg/ g),阿魏酸(95.46μg/ g)和槲皮素(3.17μg/ g)是定量的主要多酚在PP提取物中。 PP的体外抗氧化能力由三价铁还原抗氧化剂电位(31.86μMFe + 2 / g),trolox当量抗氧化剂能力(14.56 mM trolox当量(TE)/ g),氧自由基清除活性(30.88 mM TE / g)确定)和2,2-二苯基-1-吡啶并肼基清除能力(IC50-8.33 mg / ml)。与对照组相比,诱导氧化应激显着(p≤0.05)将SOD,CAT,GPx,GR活性和GSH水平降低了3.1、1.46、2.87、1.34和1.32倍。然而,与氧化应激诱导的细胞相比,用PP提取物处理细胞显着(p≤0.05)增强了SOD,CAT,GPx,GR活性和GSH。用PP提取物处理细胞会显着(p≤0.05)降低COX-2活性,增强caspase-3活性并诱导DNA断裂,表明PP提取物通过凋亡导致细胞死亡。总之,PP提取物的抗癌特性可能归因于自由基清除能力,诱导抗氧化酶和诱导细胞凋亡的协同作用。

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