Harasty J, Halliday G M, Kril J J
Department of Pathology, University of Sydney, NSW, Australia
J Neurosci Methods. 1996 Jul;67(1):43-51.
The variability in the external gyri pattern of human brains has made the identification of specific cortical areas difficult. Studies correlating cortical structure and function have not consistently controlled for this variability. The aim of the present study was to develop a reliable and reproducible regimen for sampling five speech-associated and one non-speech associated cortical region in the human brain. The gyri of interest were labelled using non-aqueous dye prior to coronal slicing of brains at 3 mm intervals. Using the labelled gyri, a set of internal brain landmarks was established to aid in sampling one block of each cortical region of interest. The position of each internal landmark was determined as a percentage of the total brain length and breadth. The variability in the position of each internal landmark was investigated using analysis of variance and found to be consistent in three dimensions in all cases. The correlation of the sampled cortical region to the internal landmark was consistent in different cases with point to point agreement of 100%. This contrasts with the variability between cases in external gyri features. The sampled region was tested to determine cytoarchitectural variability by measuring the depth of each cortical layer. This technique found that the same cytoarchitectural regions were sampled in each case. As expected, these regions were distinguishable by the significant difference in the depth of different cortical layers. Accurate identification of both the external gyri and internal landmarks occurred with interrater point to point agreement of 90-100%.
人类大脑外部脑回模式的变异性使得特定皮质区域的识别变得困难。将皮质结构与功能相关联的研究并未始终如一地控制这种变异性。本研究的目的是开发一种可靠且可重复的方案,用于在人脑中对五个与言语相关和一个与非言语相关的皮质区域进行采样。在将大脑以3毫米间隔进行冠状切片之前,使用非水性染料标记感兴趣的脑回。利用标记的脑回,建立了一组脑内标志物,以帮助对每个感兴趣的皮质区域的一个块进行采样。每个脑内标志物的位置被确定为整个大脑长度和宽度的百分比。使用方差分析研究了每个脑内标志物位置的变异性,发现在所有情况下三维方向上都是一致的。在不同情况下,采样的皮质区域与脑内标志物的相关性是一致的,点对点一致性为100%。这与外部脑回特征在不同病例之间的变异性形成对比。通过测量每个皮质层的深度,对采样区域进行测试以确定细胞结构变异性。该技术发现,在每种情况下都采样到了相同的细胞结构区域。正如预期的那样,这些区域可通过不同皮质层深度的显著差异来区分。外部脑回和脑内标志物的准确识别在评分者间点对点一致性为90%至100%的情况下实现。