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氧化损伤与运动神经元疾病:人脑组织中蛋白质羰基测量的困难

Oxidative damage and motor neurone disease difficulties in the measurement of protein carbonyls in human brain tissue.

作者信息

Lyras L, Evans P J, Shaw P J, Ince P G, Halliwell B

机构信息

Neurodegenerative Disease Research Centre, King's College, London, UK.

出版信息

Free Radic Res. 1996 May;24(5):397-406. doi: 10.3109/10715769609088038.

Abstract

It has been suggested in the literature that elevated oxidative protein damage, measured as protein carbonyls, is present in the nervous system of patients with sporadic motor neurone disease (MND). However, the actual reported levels of brain protein carbonyls vary over a wide range. We show here that this is probably due to the use of the different protocols for the carbonyl assay; results differ depending on when the dinitrophenylhydrazine reagent is added and at what stage in the procedure protein is assayed for the calculation of carbonyls on a unit protein basis. Using a range of different procedures, we were unable to confirm reports of elevated protein carbonyls in motor cortex from brains of patients with MND. We also measured thiobarbituric acid-reactive material in the brain samples using an HPLC-based TBA test in the presence of butylated hydroxytoluene. In general, there was no significant elevation of TBARS in MND motor cortex. However, four patients showed values higher than any of the control patients (both 'normal' control and 'disease control'). There was no correlation of TBARS with protein carbonyl values. We suggest that oxidative damage in motor cortex in sporadic MND, if it occurs, may be confined to a small group of patients and may affect different molecular targets in each patient.

摘要

文献中曾指出,以蛋白质羰基含量衡量的氧化蛋白质损伤在散发性运动神经元病(MND)患者的神经系统中存在。然而,实际报道的脑蛋白质羰基含量水平差异很大。我们在此表明,这可能是由于羰基测定采用了不同的方案;结果因二硝基苯肼试剂添加的时间以及在计算单位蛋白质羰基含量时蛋白质测定所处的程序阶段而异。通过一系列不同的程序,我们无法证实MND患者大脑运动皮质中蛋白质羰基含量升高的报道。我们还在丁基化羟基甲苯存在的情况下,使用基于高效液相色谱的硫代巴比妥酸试验测量了脑样本中的硫代巴比妥酸反应性物质。总体而言,MND运动皮质中的硫代巴比妥酸反应物(TBARS)没有显著升高。然而,有四名患者的数值高于任何对照患者(“正常”对照和“疾病”对照)。TBARS与蛋白质羰基值之间没有相关性。我们认为,散发性MND运动皮质中的氧化损伤(如果发生的话)可能局限于一小部分患者,并且可能在每个患者中影响不同的分子靶点。

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