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Eadioprotective Effects of Gallic Acid in Mice

机译:没食子酸对小鼠的保护作用

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摘要

Radioprotecting ability of the natural polyphenol, gallic acid (3,4,5-trihydroxybenzoic acid, GA), was investigated in Swiss albino mice. Oral administration of GA (100 mg/kg body weight), one hour prior to whole body gamma radiation exposure (2-8 Gy; 6 animals/group), reduced the radiation-induced cellular DNA damage in mouse peripheral blood leukocytes, bone marrow cells, and spleenocytes as revealed by comet assay. The GA administration also prevented the radiation-induced decrease in the levels of the antioxidant enzyme, glutathione peroxidise (GPx), and nonprotein thiol glutathione (GSH) and inhibited the peroxidation of membrane lipids in these animals. Exposure of mice to whole body gamma radiation also caused the formation of micronudei in blood reticulocytes and chromosomal aberrations in bone marrow cells, and the administration of GA resulted in the inhibition of micronucleus formation and chromosomal aberrations. In irradiated animals, administration of GA elicited an enhancement in the rate of DNA repair process and a significant increase in endogenous spleen colony formation. The administration of GA also prevented the radiation-induced weight loss and mortality in animals (10 animals/group) exposed to lethal dose (10 Gy) of gamma radiation. (For every experiment unirradiated animals without GA administration were taken as normal control; specific dose (Gy) irradiated animals without GA administration serve as radiation control; and unirradiated GA treated animals were taken as drug alone control).
机译:在瑞士的白化病小鼠中研究了天然多酚没食子酸(3,4,5-三羟基苯甲酸,GA)的辐射防护能力。在全身伽马射线辐射(2-8 Gy; 6只动物/组)之前一小时口服GA(100 mg / kg体重),减少了小鼠外周血白细胞,骨髓中辐射诱导的细胞DNA损伤彗星试验揭示的细胞和脾细胞。 GA的使用还可以防止辐射诱导的抗氧化酶,谷胱甘肽过氧化物(GPx)和非蛋白硫醇谷胱甘肽(GSH)的水平降低,并抑制了这些动物中膜脂质的过氧化。小鼠暴露于全身伽马射线还会引起血液网织细胞中微核的形成和骨髓细胞中的染色体畸变,而GA的给药导致微核形成和染色体畸变受到抑制。在受辐照的动物中,GA的使用引起DNA修复过程速率的提高和内源性脾脏集落形成的显着增加。 GA的使用还可以防止受到致命剂量(10 Gy)γ射线照射的动物(每组10只动物)的辐射诱发的体重减轻和死亡率。 (对于每个实验,将未施用GA的未辐照动物作为正常对照;将未施用GA的特定剂量(Gy)辐照的动物用作辐照对照;将未经辐照的GA处理的动物作为单独药物对照)。

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