Cullen K M, Halliday G M, Double K L, Brooks W S, Creasey H, Broe G A
School of Biological Sciences and Department of Pathology, University of Sydney, Australia.
Neuroscience. 1997 Jun;78(3):641-52. doi: 10.1016/s0306-4522(96)00569-6.
Cortical atrophy and cell loss in the cholinergic nucleus basalis is a well-established characteristic of Alzheimer's disease; however, previous studies not have analysed cholinergic cell loss and cortical atrophy in concert. In autopsy brains from eight patients with Alzheimer's disease and 12 control subjects, the numbers of nucleus basalis neurons were determined from 50-microm serial Nissl-stained sections. Volumes of the cerebrum, cortical gray matter (total, lobar and subregional), white matter and deep gray structures were computed by point counting on black and white photographs of gapless 3-mm coronal slices of formalin-fixed brains. Cell loss in the nucleus basalis was found to range between 89% and 42% in Alzheimer's disease compared with controls. White matter volume was unchanged in absolute terms in Alzheimer's disease patients compared with controls, while cortical volume was significantly reduced. Gray matter atrophy was most prominent in temporal and frontal cortices. A highly significant linear relationship was found between cortical volume and nucleus basalis cell number in controls and Alzheimer's disease patients, with values for both groups on a single regression line. Whole brain and cerebral volumes were also highly correlated to nucleus basalis cell numbers in both groups. A quantitative analysis of plaque and tangle burden in cortical target areas of the nucleus basalis was performed. In contrast to the relationship with cortical volume, nucleus basalis cell number and neurofibrillary tangle number were not significantly correlated to the density of cortical histopathology. These results suggest that the volume of cortical gray matter is coupled to the number of nucleus basalis neurons. Compromised viability of nucleus basalis neurons may precede cortical volume loss as large numbers of neurofibrillary tangles, detected with nickel peroxidase staining, were found in this nucleus in all Alzheimer's disease cases, including those with minimal cell loss.
胆碱能基底核的皮质萎缩和细胞丢失是阿尔茨海默病公认的特征;然而,以往的研究并未同时分析胆碱能细胞丢失和皮质萎缩情况。在8例阿尔茨海默病患者和12例对照受试者的尸检大脑中,从50微米连续尼氏染色切片中确定基底核神经元的数量。通过对福尔马林固定大脑的3毫米无间隙冠状切片的黑白照片进行点计数,计算大脑、皮质灰质(总体、叶和亚区域)、白质和深部灰质结构的体积。与对照组相比,发现阿尔茨海默病患者基底核中的细胞丢失率在89%至42%之间。与对照组相比,阿尔茨海默病患者的白质体积绝对值没有变化,而皮质体积显著减少。灰质萎缩在颞叶和额叶皮质最为明显。在对照组和阿尔茨海默病患者中,发现皮质体积与基底核细胞数量之间存在高度显著的线性关系,两组的值在同一条回归线上。两组中全脑和大脑体积也与基底核细胞数量高度相关。对基底核皮质靶区的斑块和缠结负荷进行了定量分析。与皮质体积的关系不同,基底核细胞数量与神经原纤维缠结数量与皮质组织病理学密度没有显著相关性。这些结果表明,皮质灰质体积与基底核神经元数量相关。基底核神经元活力受损可能先于皮质体积减少,因为在所有阿尔茨海默病病例中,包括那些细胞丢失最少的病例,在该核中都发现了大量用镍过氧化物酶染色检测到的神经原纤维缠结。