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首页> 外文期刊>Biomedicine & preventive nutrition >Protective effects of deferiprone and desferrioxamine in brain tissue of aluminum intoxicated mice: An FTIR study
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Protective effects of deferiprone and desferrioxamine in brain tissue of aluminum intoxicated mice: An FTIR study

机译:去铁酮和去铁胺对铝中毒小鼠脑组织的保护作用:FTIR研究

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摘要

The present study was designed to study aluminum chloride which caused marked alterations in biochemical parameters such as glutathione peroxidase, catalase, superoxide dismutase, and TBARS in brain tissues of mice. Fourier transform infrared spectroscopy spectra reflect the alterations on major biochemical constituents in brain tissues of mice such as proteins, lipids and nucleic acids due to the overproduction of ROS. Furthermore, administration of deferiprone and deferoxamine significantly improved the level of protein and shifted back the peak positions of amide I and II to near control values indicating tau protein, β-amyloid, amyloid plaques and neurofibrillary tangles decreased, consequently protected from Alzheimer's disease and other major risk factor of many neuronal dysfunctions in brain tissues. Therefore, aluminum toxicity is a widespread crisis to all living organisms, including both flora and fauna. Furthermore, it causes widespread degradation of the environment and health. Therefore, the present investigation suggested that DFO and DFP are efficient chelators for aluminum poisoning and they reduced the aluminum concentration.
机译:本研究旨在研究氯化铝,该氯化铝在小鼠脑组织中引起生化参数的显着改变,例如谷胱甘肽过氧化物酶,过氧化氢酶,超氧化物歧化酶和TBARS。傅里叶变换红外光谱图反映了由于过度生产ROS而引起的小鼠脑组织主要生物化学成分(如蛋白质,脂质和核酸)的变化。此外,施用去铁酮和去铁胺可显着提高蛋白质水平,并将酰胺I和II的峰位移回至接近控制值,表明tau蛋白,β-淀粉样蛋白,淀粉样蛋白斑块和神经原纤维缠结减少,因此可预防阿尔茨海默氏病和其他疾病脑组织中许多神经元功能障碍的主要危险因素。因此,铝毒性是对所有活生物体(包括动植物群)的普遍威胁。此外,它导致环境和健康的广泛恶化。因此,本研究表明DFO和DFP是铝中毒的有效螯合剂,它们降低了铝的浓度。

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