Department of Biochemistry of Biotechnology, Faculty of Science, Annamalai University, Annamalainagar 608002, Tamil Nadu, India.
Eur J Pharmacol. 2011 Dec 15;672(1-3):20-9. doi: 10.1016/j.ejphar.2011.09.003. Epub 2011 Sep 21.
The purpose of this study was to investigate the antioxidant potential of umbelliferone, 7-hydroxy coumarin, and its role in the protection against radiation-induced oxidative damage in cultured human blood lymphocytes. It was found that the antioxidant effect of umbelliferone was dose dependent in hydroxyl (OH(•)), superoxide anion (O(2)(•-)), 2,2-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid radical cation (ABTS(•+)) and 1,1-diphenyl-2-picrylhydrazyl (DPPH(•)) radical scavenging assays. To explore the radioprotective effect of umbelliferone, freshly isolated human blood lymphocytes were treated with 124 μM umbelliferone (optimum dose-fixed by MTT assay) 30 min before 3Gy irradiation. It was found that umbelliferone pretreatment inhibited radiation-induced reactive oxygen species generation in 3Gy exposed lymphocytes. Microscopic observations showed that there was a significant apoptotic cells (ethidium bromide/acridine orange staining) and decreased mitochondrial membrane potential (Rhodamine 123 staining) in irradiated lymphocytes. On the other hand, 124 μM umbelliferone treatment significantly decreased % of apoptotic cells and prevented radiation induced mitochondrial depolarization in lymphocytes. Further, it was noticed that there was an increased DNA damage (comet assay), lipid peroxidation with decreased antioxidant enzymatic i.e., superoxide dismutase, catalase and, glutathione peroxidase activities in 3Gy irradiated lymphocytes. Conversely, umbelliferone (124 μM) treatment before irradiation decreased comet attributes and lipid peroxidative markers with improved antioxidant enzyme activities in irradiated lymphocytes. Taken together, the results of this study clearly suggest the radioprotective effect of umbelliferone in human lymphocytes by inhibiting reactive oxygen species generation and its subsequent toxicity.
本研究旨在探讨伞形酮、7-羟基香豆素的抗氧化潜力及其在保护培养的人血淋巴细胞免受辐射诱导的氧化损伤中的作用。结果发现,伞形酮在羟自由基(OH(•))、超氧阴离子自由基(O(2)(•-))、2,2-偶氮-双-3-乙基苯并噻唑啉-6-磺酸自由基阳离子(ABTS(•+))和 1,1-二苯基-2-苦基肼基自由基(DPPH(•))清除实验中具有剂量依赖性的抗氧化作用。为了探讨伞形酮的辐射防护作用,我们将新鲜分离的人血淋巴细胞用 124μM 伞形酮(MTT 测定法确定的最佳剂量)处理 30 分钟,然后进行 3Gy 照射。结果发现,伞形酮预处理可抑制 3Gy 照射后淋巴细胞中活性氧的产生。显微镜观察显示,在辐照的淋巴细胞中存在明显的凋亡细胞(溴化乙锭/吖啶橙染色)和线粒体膜电位降低(罗丹明 123 染色)。另一方面,124μM 伞形酮处理可显著降低凋亡细胞的%,并防止辐射诱导的淋巴细胞中线粒体去极化。此外,我们注意到,在 3Gy 辐照的淋巴细胞中,DNA 损伤(彗星试验)增加,抗氧化酶如超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶的活性降低,脂质过氧化。相反,辐照前用 124μM 伞形酮处理可降低彗星参数和脂质过氧化标志物,并改善辐照淋巴细胞中的抗氧化酶活性。总之,本研究结果清楚地表明,伞形酮通过抑制活性氧的产生及其随后的毒性,对人淋巴细胞具有辐射防护作用。