首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Radioprotective effect of sesamol on gamma-radiation induced DNA damage, lipid peroxidation and antioxidants levels in cultured human lymphocytes.
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Radioprotective effect of sesamol on gamma-radiation induced DNA damage, lipid peroxidation and antioxidants levels in cultured human lymphocytes.

机译:芝麻酚对γ-射线诱导的人淋巴细胞中DNA损伤,脂质过氧化和抗氧化剂水平的辐射防护作用。

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摘要

Sesamol pretreated (1, 5 and 10 microg/ml) lymphocytes were exposed to different doses of gamma-radiation, i.e., 1, 2 and 4 Gray (Gy) and the cellular changes were estimated by using cytokinesis blocked micronucleus assay (MN), dicentric aberration (DC), thiobarbituric acid reactive substances (TBARS), reduced glutathione (GSH) and the activities of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx). Radiation significantly increased MN, DC frequencies, TBARS levels and decreased GSH and antioxidant enzyme levels in a dose dependent manner. The highest damage to lymphocytes was observed at 4 Gy irradiation. On the other hand, sesamol pretreatment significantly decreased MN, DC frequencies, TBARS levels and increased GSH levels and SOD, CAT and GPx activities in a concentration dependent manner. At 1 Gy irradiation all concentrations of sesamol (1, 5 and 10 microg/ml) significantly protects the lymphocytes from radiation damage. At 2 Gy irradiation 5 and 10 microg/ml of sesamol shows significant radioprotection. Since the highest damage was observed at 4 Gy irradiation both 1 and 5 microg/ml of sesamol pretreatment were not sufficient to protect the lymphocytes from radiation damage but 10 microg/ml of sesamol significantly (p<0.05) protects the lymphocytes from radiation effect. Thus, sesamol pretreatment gives significant protection to cultured human lymphocytes against gamma-radiation induced cellular damage. The possible mechanism involved in the radioprotective influence of sesamol is discussed.
机译:将Sesamol预处理的(1、5和10 microg / ml)淋巴细胞暴露于不同剂量的γ射线照射,即1、2和4 Gray(Gy),并通过胞质分裂封闭微核试验(MN)估算细胞的变化,双中心像差(DC),硫代巴比妥酸反应性物质(TBARS),还原型谷胱甘肽(GSH)以及超氧化物歧化酶(SOD),过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPx)的活性。辐射以剂量依赖性方式显着增加了MN,DC频率,TBARS水平,并降低了GSH和抗氧化酶水平。在4 Gy照射下观察到对淋巴细胞的最高损伤。另一方面,芝麻酚预处理以浓度依赖性方式显着降低了MN,DC频率,TBARS水平并增加了GSH水平以及SOD,CAT和GPx活性。在1 Gy辐射下,所有浓度的芝麻酚(1、5和10 microg / ml)均能显着保护淋巴细胞免受辐射损害。在2 Gy照射下5和10微克/毫升的芝麻酚显示出显着的辐射防护作用。由于在4 Gy辐射下观察到最高的损伤,因此1和5μg/ ml的芝麻酚预处理均不足以保护淋巴细胞免受辐射损伤,但是10μg/ ml的芝麻酚显着(p <0.05)保护淋巴细胞免受辐射作用。因此,芝麻酚预处理可为培养的人类淋巴细胞提供显着的保护,使其免受伽马射线引起的细胞损伤。讨论了芝麻酚的辐射防护作用的可能机制。

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