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Dietary intake of antioxidant supplements modulate antioxidant status and heat shock protein 70 synthesis

机译:膳食摄入抗氧化剂补充剂可调节抗氧化剂状态和热休克蛋白70的合成

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摘要

The physiological effects and efficacy of dietary intake of antioxidant supplements in humans remains controversial. Experiments involving dietary, often high, intake of a single antioxidant or vitamin may be seriously flawed given the interactive nature of antioxidants in vivo. The present studies were conducted on individuals (35-60 years of age) taking a commercial antioxidant mixture in a double-blind, placebo-controlled, cross-over study. Intake was two capsules per day, for 4 weeks, with a 4-week washout period in between active dose or placebo. Intake of antioxidants was associated with little change in superoxide dismutase activity, but an increase in glutathione peroxidase was noted. Haemolysis of red blood cells (erythrocytes) induced by the free radical generator AAPH was significantly reduced in individuals on antioxidant supplements. In lymphocytes isolated from individuals taking supplements, there was a marked increase, as compared with individuals on placebo, in the synthesis of heat shock protein 70 (hsp70) following heat shock from 37°C to 42.5°C. We conclude that dietary intake of a mixed antioxidant supplement leads to modulation of cellular redox status resulting in decreased oxidative stress and increased ability of lymphocytes to mount a stress response.
机译:饮食中人类抗氧化剂补充剂的生理作用和功效尚存争议。考虑到体内抗氧化剂的相互作用,涉及饮食(通常是高摄入量)的一种抗氧化剂或维生素的实验可能存在严重缺陷。本研究是在双盲,安慰剂对照,交叉研究中,对服用商业抗氧化剂混合物的个体(35-60岁)进行的。摄入量为每天两粒胶囊,持续4周,有效剂量或安慰剂之间的清除期为4周。抗氧化剂的摄入与超氧化物歧化酶活性的变化很小,但是谷胱甘肽过氧化物酶却有所增加。使用抗氧化剂补充剂的个体中,自由基产生剂AAPH诱导的红细胞(红细胞)的溶血作用明显降低。与服用安慰剂的个体相比,从服用补充剂的个体分离的淋巴细胞中,从37°C到42.5°C的热激后,热激蛋白70(hsp70)的合成显着增加。我们得出的结论是,饮食中混合抗氧化剂的摄入会导致细胞氧化还原状态的调节,从而导致氧化应激降低和淋巴细胞增强应激反应的能力增强。

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  • 来源
    《Redox Report》 |2002年第5期|308-311|共4页
  • 作者单位

    Human Biology, School of Biological Sciences, University of New England, Armidale, New South Wales, Australia;

    Human Biology, School of Biological Sciences, University of New England, Armidale, New South Wales, Australia;

    Blackmores Research Centre, Southern Cross University, Lismore, New South Wales, Australia;

    Human Biology, School of Biological Sciences, University of New England, Armidale, New South Wales, Australia;

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