首页> 外文期刊>BARC Newsletter >ROLE OF MEMBRANE OXIDATIVE DAMAGE AND REACTIVE OXYGEN SPECIES IN RADIATION INDUCED APOPTOTIC DEATH IN MOUSE THYMOCYTES
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ROLE OF MEMBRANE OXIDATIVE DAMAGE AND REACTIVE OXYGEN SPECIES IN RADIATION INDUCED APOPTOTIC DEATH IN MOUSE THYMOCYTES

机译:膜氧化损伤和活性氧在辐射诱导小鼠胸腺细胞凋亡中的作用。

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Involvement of membrane damage and reactive oxygen species (ROS) in mechanism of radiation induced apoptotic death were investigated in mouse thymocytes in presence of eugenol, a membrane specific antioxidant from plant sources. The membrane damage in thymocytes by gamma-irradiation was determined by measurement of thiobarbituric acid reactive species (TEARS). Generation of reactive oxygen species and apoptosis in irradiated thymocytes was estimated by using fluorescence probes, 2,7-dichlorodihydrofluorescien diacetate (DCH-FDA) and annexin-V method, respectively. The radiation response of thymocytes for ROS generation was found to be dependent on radiation dose and dose rate. DCH-FDA fluorescence appears sensitive for detection of radiation exposures at low doses, and a dose of 0.5 cGy and 0.5 Gy was detected for the dose rate of 0.45 cGy / min. and 0.5 Gy / min, respectively. Lipid peroxidation was inhibited in irradiated (2 Gy) thymocytes with increasing concentrations of eugenol (10-200 mu M) treated prior to irradiation. The concentration of eugenol required to inhibit half of the MDA formation (IC_(50)) in irradiated thymocytes was 100 juM. Percentage apoptosis in irradiated thymocytes was significantly inhibited by these antioxidants, which was however, more effective inhibited by lipophilic antioxidants. The results suggest the linkage of radiation generated membrane damage and ROS in the mechanism of apoptotic death in thymocytes.
机译:在丁香酚(一种来自植物的膜特异性抗氧化剂)存在下,在小鼠胸腺细胞中研究了膜损伤和活性氧(ROS)在辐射诱导的凋亡死亡机制中的参与。通过测量硫代巴比妥酸反应性物种(TEARS)来确定γ射线对胸腺细胞的膜损伤。分别使用荧光探针,2,7-二氯二氢荧光二乙酸二乙酸酯(DCH-FDA)和Annexin-V方法估计了辐射的胸腺细胞中活性氧的产生和凋亡。发现胸腺细胞产生ROS的放射反应取决于放射剂量和剂量率。 DCH-FDA荧光似乎对检测低剂量的放射线敏感,对于0.45 cGy / min的剂量率,检测到0.5 cGy和0.5 Gy的剂量。和0.5 Gy / min。辐照前处理的丁香酚浓度(10-200μM)增加,在辐照的(2 Gy)胸腺细胞中脂质过氧化受到抑制。抑制辐射胸腺细胞中MDA形成一半(IC_(50))所需的丁子香酚浓度为100 juM。这些抗氧化剂显着抑制了辐射胸腺细胞的凋亡百分比,然而,亲脂性抗氧化剂更有效地抑制了百分比。结果表明,辐射产生的膜损伤与ROS在胸腺细胞凋亡死亡机制中的联系。

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