Watt F
Nuclear Microscopy Group, Physics Department, National University of Singapore.
Cell Mol Biol (Noisy-le-grand). 1996 Feb;42(1):17-26.
The scanning nuclear microprobe (nuclear microscope) is becoming a powerful instrument for the accurate measurement of minor and trace elements in biological tissue. Using the simultaneously applied techniques of Scanning Transmission Ion Microscopy (STIM) to image features in the tissue, Particle induced X-ray emission (PIXE) to measure trace element concentrations, and Rutherford Backscattering Spectrometry (RBS) to characterize the tissue matrix, accurate elemental analysis at the parts per million level can be obtained for most elements. This review describes briefly the results obtained using the nuclear microscope for the elemental analysis of Alzheimer's and Parkinson's tissue. In Alzheimer's disease (AD) the identification and subsequent analysis of neuritic plaque cores in unstained tissue, yielded an absence of aluminium at the limit of 15 parts per million. Previous analyses involving stained sections were prone to misinterpretation due to aluminium contamination from the staining procedures. Elemental iron, calcium, phosphorus and sulphur were elevated both in the plaques and the AD background tissue compared to age matched controls. Preliminary analyses of neurofibrillary tangles stained with toluidine blue showed increased levels of calcium, although the staining procedure may have distorted the results due to element redistribution. In Parkinson's disease (PD) nuclear microscope studies have concentrated on measurements of iron in the substantia nigra (SN) region of the brain; iron was observed to be elevated by a factor 2 in MPTP induced Parkinsonism in African Green monkeys, and by a factor of 1.25 in 6-OHDA induced Parkinsonism in Sprague Dawley rats. These studies are consistent with other studies showing a general increase in the concentrations of iron associated with PD, and support the theory that iron mediated free radical production may enhance or accelerate the degeneration of dopaminergic cells through oxidative stress.
扫描核微探针(核显微镜)正成为一种用于精确测量生物组织中微量元素的强大仪器。利用同时应用的扫描透射离子显微镜(STIM)技术对组织特征进行成像、粒子诱导X射线发射(PIXE)技术测量微量元素浓度以及卢瑟福背散射光谱(RBS)技术表征组织基质,对于大多数元素而言,能够获得百万分之一水平的精确元素分析结果。本综述简要描述了使用核显微镜对阿尔茨海默病和帕金森病组织进行元素分析所取得的结果。在阿尔茨海默病(AD)中,对未染色组织中的神经炎性斑块核心进行识别并随后分析,结果显示铝含量低于百万分之15的检测限。先前涉及染色切片的分析由于染色过程中的铝污染而容易产生误解。与年龄匹配的对照组相比,斑块和AD背景组织中的元素铁、钙、磷和硫含量均有所升高。用甲苯胺蓝染色的神经原纤维缠结的初步分析显示钙含量增加,尽管染色过程可能因元素重新分布而使结果产生偏差。在帕金森病(PD)中,核显微镜研究主要集中在对大脑黑质(SN)区域铁含量的测量;在非洲绿猴的MPTP诱导的帕金森病中,铁含量升高了2倍,在Sprague Dawley大鼠的6 - OHDA诱导的帕金森病中,铁含量升高了1.25倍。这些研究与其他显示与PD相关的铁浓度普遍增加的研究一致,并支持铁介导的自由基产生可能通过氧化应激增强或加速多巴胺能细胞变性的理论。