Harish G, Venkateshappa C, Mahadevan Anita, Pruthi Nupur, Bharath M M Srinivas, Shankar S K
1 Department of Neurochemistry, National Institute of Mental Health and Neurosciences (NIMHANS) , Bangalore, India .
Biopreserv Biobank. 2011 Dec;9(4):379-87. doi: 10.1089/bio.2011.0033. Epub 2011 Nov 10.
Biochemical analyses of many brain diseases have highlighted that oxidative damage of proteins and astrogliosis are important events associated with pathology. However, human studies on the status of protein oxidation/nitration and astrogliosis [indicated by expression of glial fibrillary acidic protein (GFAP)] heavily depend on postmortem tissues that might be altered by pre and postmortem factors. To evaluate the effect of these variables, we tested whether the status of GFAP expression, oxidized proteins, and nitrated proteins (by protein 3-nitrotyrosine or 3-NT) were affected in postmortem human brains (n=48) by increased storage time (11.8-104.1 months), postmortem interval (PMI) (2.5-26 h), gender difference, and agonal state (based on Glasgow coma scale: range: 3-15) in different anatomical regions-frontal cortex (FC), cerebellum (CB) and medulla oblongata (MD). We observed that increasing storage time significantly decreased the stability of all 3 markers in MD (oxyblot: P=0.003; 3-NT: P=0.01; GFAP: P=0.03) and that of oxidized proteins in CB (P=0.04), whereas the status of all markers was not significantly altered in FC. On the other hand, PMI and agonal state did not influence the status of all the markers tested in any of the regions. Similarly, except for the decreased protein 3-NT among women in CB compared with men (P=0.04), there was no effect due to gender differences in other brain regions for other markers. These data highlight the influence of storage time on preservation of markers of protein damage and astrogliosis and the inherent differences in brain regions, with implications for studies on brain pathology employing stored human samples.
对许多脑部疾病的生化分析表明,蛋白质的氧化损伤和星形胶质细胞增生是与病理相关的重要事件。然而,关于蛋白质氧化/硝化状态和星形胶质细胞增生[通过胶质纤维酸性蛋白(GFAP)的表达来指示]的人体研究严重依赖于死后组织,而这些组织可能会受到生前和死后因素的影响。为了评估这些变量的影响,我们测试了在不同解剖区域——额叶皮质(FC)、小脑(CB)和延髓(MD)中,死后人类大脑(n = 48)中GFAP表达、氧化蛋白和硝化蛋白(通过蛋白质3-硝基酪氨酸或3-NT)的状态是否会受到储存时间增加(11.8 - 104.1个月)、死后间隔(PMI)(2.5 - 26小时)、性别差异和濒死状态(基于格拉斯哥昏迷量表:范围:3 - 15)的影响。我们观察到,储存时间的增加显著降低了MD中所有3种标志物的稳定性(氧化印迹法:P = 0.003;3-NT:P = 0.01;GFAP:P = 0.03)以及CB中氧化蛋白的稳定性(P = 0.04),而FC中所有标志物的状态没有显著改变。另一方面,PMI和濒死状态在任何区域都没有影响所测试的所有标志物的状态。同样,除了CB中女性的蛋白质3-NT比男性减少(P = 0.04)外,其他脑区中其他标志物的性别差异没有影响。这些数据突出了储存时间对蛋白质损伤和星形胶质细胞增生标志物保存的影响以及脑区的固有差异,这对使用储存的人类样本进行脑病理学研究具有重要意义。