Di Lorenzo Alho Ana Tereza, Suemoto Claudia Kimie, Polichiso Lívia, Tampellini Edilaine, de Oliveira Kátia Cristina, Molina Mariana, Santos Glaucia Aparecida Bento, Nascimento Camila, Leite Renata Elaine Paraizo, de Lucena Ferreti-Rebustini Renata Eloah, da Silva Alexandre Valotta, Nitrini Ricardo, Pasqualucci Carlos Augusto, Jacob-Filho Wilson, Heinsen Helmut, Grinberg Lea Tenenholz
Grupo de Estudos em Envelhecimento Cerebral e LIM 22, Department of Pathology, Faculdade de Medicina da Universidade de Sao Paulo, Av. Dr. Arnaldo, 455 sala 1353, São Paulo, CEP 01246-903, Brazil.
Labor für Morphologische Hirnforschung der Klinik und Poliklinik für Psychiatrie und Psychotherapie, Institut Rechtsmedizin, Universitätsklinikum Würzburg, Würzburg, Germany.
Brain Struct Funct. 2016 Sep;221(7):3393-403. doi: 10.1007/s00429-015-1108-6. Epub 2015 Sep 19.
The human brain undergoes non-uniform changes during aging. The substantia nigra (SN), the source of major dopaminergic pathways in the brain, is particularly vulnerable to changes in the progression of several age-related neurodegenerative diseases. To establish normative data for high-resolution imaging, and to further clinical and anatomical studies we analyzed SNs from 15 subjects aged 50-91 cognitively normal human subjects without signs of parkinsonism. Complete brains or brainstems with substantia nigra were formalin-fixed, celloidin-mounted, serially cut and Nissl-stained. The shapes of all SNs investigated were reconstructed using fast, high-resolution computer-assisted 3D reconstruction software. We found a negative correlation between age and SN volume (p = 0.04, rho = -0.53), with great variability in neuronal numbers and density across participants. The 3D reconstructions revealed SN inter- and intra-individual variability. Furthermore, we observed that human SN is a neuronal reticulum, rather than a group of isolated neuronal islands. Caution is required when using SN volume as a surrogate for SN status in individual subjects. The use of multimodal sequences including those for fiber tracts may enhance the value of imaging as a diagnostic tool to assess SN in vivo. Further studies with a larger sample size are needed for understanding the structure-function interaction of human SN.
人类大脑在衰老过程中会经历不均匀的变化。黑质(SN)作为大脑主要多巴胺能通路的来源,在几种与年龄相关的神经退行性疾病进展过程中尤其容易发生变化。为了建立高分辨率成像的标准数据,并推进临床和解剖学研究,我们分析了15名年龄在50 - 91岁、认知正常且无帕金森症状迹象的人类受试者的黑质。将完整的大脑或带有黑质的脑干用福尔马林固定,火棉胶包埋,连续切片并进行尼氏染色。使用快速、高分辨率的计算机辅助三维重建软件对所有研究的黑质形状进行重建。我们发现年龄与黑质体积之间存在负相关(p = 0.04,rho = -0.53),参与者之间神经元数量和密度存在很大差异。三维重建揭示了黑质个体间和个体内的变异性。此外,我们观察到人类黑质是一个神经元网状结构,而不是一组孤立的神经元岛。在将黑质体积用作个体受试者黑质状态的替代指标时需要谨慎。使用包括纤维束序列在内的多模态序列可能会提高成像作为体内评估黑质诊断工具的价值。需要进行更大样本量的进一步研究以了解人类黑质的结构 - 功能相互作用。