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首页> 外文期刊>British Journal of Nutrition >Development of nutritional iron deficiency in growing male rats:haematological parameters, iron bioavailability and oxidative defence
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Development of nutritional iron deficiency in growing male rats:haematological parameters, iron bioavailability and oxidative defence

机译:生长中雄性大鼠营养铁缺乏症的发展:血液学参数,铁的生物利用度和氧化防御

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Despite Fe deficiency having been widely studied, the sequence of events in its development still remains unclear. The aim of the presentnstudy was to elucidate the effects of nutritional Fe-deficiency development on haematological parameters, Fe bioavailability and thenenzymes involved in oxidative defence in recently weaned male Wistar albino rats. Control (C) and Fe-deficient (ID) groups were fednthe AIN-93 G diet with a normal Fe level (45mg/kg diet) or with a low Fe level (5mg/kg diet), respectively, for 20, 30 or 40 d. At dayn20 serum Fe, serum ferritin and the saturation of transferrin decreased drastically, decreasing further in the course of Fe-deficiencyndevelopment for the saturation of transferrin. The development of Fe deficiency did not affect plasma thiobarbituric acid-reactive substancenproduction, or catalase (CAT) and glutathione peroxidase (GPx) activities in erythrocyte cytosol. Fe deficiency diminished hepatic Fe con-ntent and CAT and GPx activities in hepatic cytosol only at day the 20. However, in spite of the minor Fe deposits in the brain of ID rats, thenCAT and GPx activities in the brain cytosolic fraction did not differ in any of the studied periods v. control rats. These results show thatnbrain is a tissue that does not seem to depend on Fe levels for the maintenance of antioxidant defence mechanisms in the course of nutri-ntional Fe deficiency.
机译:尽管已对铁缺乏症进行了广泛研究,但其发展过程的顺序仍然不清楚。本研究的目的是阐明营养缺陷型铁的发育对最近断奶的雄性Wistar白化病大鼠血液学参数,铁生物利用度和参与氧化防御的酶的影响。对照组(C)和铁缺乏症(ID)组分别饲喂正常Fe水平(45mg / kg饮食)或低Fe水平(5mg / kg饮食)的AIN-93 G饮食,持续20、30或40天在第20天,血清铁,血清铁蛋白和转铁蛋白的饱和度急剧下降,在铁缺乏的过程中,铁蛋白的饱和度进一步降低。铁缺乏症的发展并不影响血浆硫代巴比妥酸反应性物质的产生,也不影响红细胞胞浆中的过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPx)活性。 Fe缺乏仅在第20天就降低了肝中的Fe含量以及肝细胞溶胶中的CAT和GPx活性。但是,尽管ID大鼠的大脑中有少量Fe沉积,但脑胞浆组分中的CAT和GPx活性没有差异在任何研究时期对对照组大鼠。这些结果表明,在营养性铁缺乏的过程中,脑组织似乎并不依赖于铁水平来维持抗氧化防御机制。

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