首页> 外文期刊>Fresenius Environmental Bulletin >EVALUATION OF THE CYTOTOXIC AND ANTIOXIDANT EFFECTS OF NON-POLAR VISCUM ALBUM L. EXTRACT (COLLECTED FROM JUNIPERUS COMMUNIS)
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EVALUATION OF THE CYTOTOXIC AND ANTIOXIDANT EFFECTS OF NON-POLAR VISCUM ALBUM L. EXTRACT (COLLECTED FROM JUNIPERUS COMMUNIS)

机译:非极性粘胶提取物的细胞毒性和抗氧化作用的评价(摘自杜鹃花属植物)

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The leaf extract of Viscum album was evaluated for its cytotoxic and anti/prooxidant activities. The CO_2 extract, which appeared as the most active in both assays, was subjected to GC/MS analysis to identify the sesquiterpenes trans-α-bergamotene (1), trans-β-farnesene (2) and vomi-foliol (3) as major extract constituents. The cytotoxic activity of the extract was assayed against EAC breast carcinoma cells and AS30D hepatoma cells in vivo. Dose response was tested with 3 dosages in experiments (1,2 and 3 mg/kg b.w.). In addition, evaluation of the antioxidant activity was performed in vivo, by measuring the status of reduced glutathione - glutathione reductase - glutathione peroxidase system (GSH/GR/GSHPx). All tested extract doses and compounds proved to be active, while compound (3) showed the best antioxidant effect. Also, compound (3) exhibited remarkable cytotoxic activity (75.2% on non-viable EAC cells, and 28.3% on non-viable AS30D cells), which was superior to that of N-acetyl-L-cysteine as control antioxidant (10.1% and 6.3% of non-viable EAC and AS30D cells, respectively). Differences in possible antioxidant activity between N-acetyl-L-cysteine and examined extract were noticed. N-acetyl-L-cysteine proved to be a strong antioxidant in vivo. On the other hand, crude extract and selected compounds exhibited mild antioxidant activity, and did not significantly affect the serum status of GSH/GR/GSHPx system and LPx. Nevertheless, the application of the crude extract and compound (3) significantly affected the mentioned systems in tumor cells by inducing oxidative stress, and significantly increasing cytotoxicity against EAC cells, but less against AS30D cells.
机译:评价了Viscum Album的叶提取物的细胞毒性和抗/抗氧化剂活性。对这两种测定中最活跃的CO_2提取物进行GC / MS分析,鉴定倍半萜烯的反式-α-佛手烯酮(1),反式-β-法呢烯(2)和vomi-叶醇(3)为主要提取物成分。在体内测定了提取物对EAC乳腺癌细胞和AS30D肝癌细胞的细胞毒活性。在实验中以3种剂量(1,2和3 mg / kg b.w.)测试剂量反应。另外,通过测量还原型谷胱甘肽-谷胱甘肽还原酶-谷胱甘肽过氧化物酶系统(GSH / GR / GSHPx)的状态,在体内进行抗氧化活性的评估。所有测试的提取物剂量和化合物均被证明具有活性,而化合物(3)显示出最佳的抗氧化作用。此外,化合物(3)表现出显着的细胞毒性活性(在非存活EAC细胞上为75.2%,在非存活AS30D细胞上为28.3%),优于作为对照抗氧化剂的N-乙酰-L-半胱氨酸(10.1%)。和6.3%的无效EAC和AS30D电池)。注意到N-乙酰基-L-半胱氨酸和所检查的提取物之间可能的抗氧化剂活性的差异。 N-乙酰基-L-半胱氨酸在体内被证明是一种强抗氧化剂。另一方面,粗提物和选定的化合物表现出适度的抗氧化活性,并没有显着影响GSH / GR / GSHPx系统和LPx的血清状态。然而,粗提物和化合物(3)的应用通过诱导氧化应激并显着增加了对EAC细胞的细胞毒性,而对AS30D细胞的毒性却显着影响了肿瘤细胞中的上述系统。

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