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瓜拉那提取物(Paullinia cupana)对亚硝基亚铁氰化钠诱导的成纤维细胞 NIH-3T3 细胞的保护作用。

The protective effects of guaraná extract (Paullinia cupana) on fibroblast NIH-3T3 cells exposed to sodium nitroprusside.

机构信息

Programa de Pós-Graduação em Bioquímica Toxicológica, Universidade Federal de Santa Maria, Av. Roraima 1000, Prédio 18, 97105900 Santa Maria, RS, Brazil.

出版信息

Food Chem Toxicol. 2013 Mar;53:119-25. doi: 10.1016/j.fct.2012.11.041. Epub 2012 Dec 5.

Abstract

The antioxidant effects of the hydro-alcoholic guaraná extract (Paullinia cupana var. sorbilis Mart.) on nitric oxide (NO) and other compounds generated from the degradation of sodium nitroprusside (SNP) in an embryonic fibroblast culture (NIH-3T3 cells) were evaluated. The guaraná bioactive compounds were initially determined by high-performance liquid chromatography: caffeine=12.240 mg/g, theobromine=6.733 mg/g and total catechins=4.336 mg/g. Cells were exposed to 10 μM SNP during a 6 h period because the cells exhibited >90% mortality at this concentration. Guaraná was added to the cultures in five concentrations (0.5, 1, 5, 10 and 20 mg/mL). The guaraná antioxidant effect was evaluated by viability assays, biochemical oxidation [lipid peroxidation, catalase and superoxide dismutase (SOD) activity] and genotoxicity (DNA Comet assay) analysis. Additionally, oxidative stress was evaluated by a 2,7-dihydrodichlorofluorescein diacetate fluorescence assay. Guaraná reverted the SNP toxicity mainly at lower concentrations (<5 mg), which decreased cell mortality, lipid peroxidation, DNA damage and cell oxidative stress as well as increased the SOD levels. These results demonstrate that guaraná has an antioxidant effect on NO metabolism in situations with higher cellular NO levels.

摘要

评估了水醇瓜拉那提取物(Paullinia cupana var. sorbilis Mart.)对一氧化氮(NO)和亚硝基铁氰化钠(SNP)降解产生的其他化合物的抗氧化作用,该提取物来自胚胎成纤维细胞培养(NIH-3T3 细胞)。首先通过高效液相色谱法测定瓜拉那生物活性化合物:咖啡因=12.240mg/g,可可碱=6.733mg/g 和总儿茶素=4.336mg/g。细胞在 6 小时内暴露于 10μMSNP 中,因为在此浓度下细胞的死亡率>90%。将瓜拉那添加到五个浓度(0.5、1、5、10 和 20mg/mL)的培养物中。通过活力测定、生化氧化(脂质过氧化、过氧化氢酶和超氧化物歧化酶(SOD)活性)和遗传毒性(DNA 彗星试验)分析来评估瓜拉那的抗氧化作用。此外,通过 2,7-二氢二氯荧光素二乙酸酯荧光法评估氧化应激。瓜拉那主要在较低浓度(<5mg)下逆转 SNP 毒性,降低细胞死亡率、脂质过氧化、DNA 损伤和细胞氧化应激,同时增加 SOD 水平。这些结果表明,瓜拉那对细胞内更高水平的 NO 代谢具有抗氧化作用。

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