Hörster W, Rivers A, Schuster B, Ettlinger G, Skreczek W, Hesse W
Department of Psychology, University of Bielefeld, F.R.G.
Behav Brain Res. 1989 Jun 1;33(2):209-27. doi: 10.1016/s0166-4328(89)80052-x.
Given the failure of the ablation method to identify the neural structures/systems that are crucial for cross-modal recognition (CMR) and for tactile discrimination performance (TDP), we injected radioactive 2-deoxy-[14C]glucose (2-DG) into monkeys trained to a high level of CMR or TDP. Nine monkeys were trained to recognize in one sense-modality, to a level greater than 80% correct, the objects experienced in the alternate modality on only a single prior trial. After injection, CMR was continued (Expt. 1a) exactly as before, except that all CMR problems were now in only one direction; or (Expt. 1b) the second--the CMR--trial of each problem was not realized (i.e. no objects were available in the second modality) so that the monkey merely 'expected' the cross-modal trial. Nine other monkeys were trained on a graded roughness discrimination task with conventional 'titration' procedures to a stable level of performance, either (Expt. 2a) without having undergone any cortical removal, or (Expt. 2b) after unilateral removal--contralateral or ipsilateral to the preferred hand--of the posterior insula or of the second somatosensory projection cortex (SII). Exactly the same training procedures were continued in Expt. 2 after injection of 2-DG. Coronal radiographs were made at 490 microns for all 18 monkeys (and also for a 19th, which served as a control in Expt. 1b). The optical densities of the autoradiographs were measured quantitatively in respect of 50 structures or part-structures (e.g. sulci, thalamic nuclei, subcortical structures); they were rated either with the aid of 'pseudo-colours' produced by the computer, or directly by judging the black/white optical densities, in respect of 29 other structures. These 79 structures were then the dependent variables in MANOVAs or ANOVAs, to determine differences between groups; or within groups with respect to the left/right and ipsilateral/contralateral hemispheres; or interaction effects. It was found that certain structures (e.g. the ventral portion of the claustrum, the insula with its extension ventrally into the fundus, nucleus Medialis dorsalis and nucleus Pulvinar oralis) repeatedly, whereas others (e.g. the amygdala) never gave rise to significant outcomes. Structures in the left cerebral hemisphere were frequently found to be more strongly labelled than those in the right hemisphere.(ABSTRACT TRUNCATED AT 400 WORDS)
鉴于消融方法未能识别出对跨模态识别(CMR)和触觉辨别能力(TDP)至关重要的神经结构/系统,我们向经过高水平CMR或TDP训练的猴子体内注射了放射性2-脱氧-[14C]葡萄糖(2-DG)。九只猴子接受训练,使其在一种感觉模态下识别仅在之前一次试验中在另一种模态下体验过的物体,识别正确率高于80%。注射后,CMR实验(实验1a)继续进行,与之前完全相同,只是所有CMR问题现在仅在一个方向上;或者(实验1b)每个问题的第二次——CMR——试验未进行(即第二种模态下没有物体可用),这样猴子只是“预期”跨模态试验。另外九只猴子通过传统的“滴定”程序在分级粗糙度辨别任务上进行训练,使其达到稳定的表现水平,要么(实验2a)未进行任何皮质切除,要么(实验2b)在单侧切除——与优势手对侧或同侧——后岛叶或第二体感投射皮层(SII)后进行训练。注射2-DG后,实验2继续进行完全相同的训练程序。对所有18只猴子(以及第19只猴子,它在实验1b中作为对照)拍摄了490微米厚的冠状X光片。对50个结构或部分结构(如脑沟、丘脑核、皮质下结构)的放射自显影片的光密度进行了定量测量;对于另外29个结构,借助计算机生成的“伪彩色”或直接通过判断黑白光密度进行评级。然后,这79个结构成为多变量方差分析(MANOVA)或方差分析(ANOVA)中的因变量,以确定组间差异;或组内关于左右半球和同侧/对侧半球的差异;或交互作用效应。结果发现,某些结构(如屏状核的腹侧部分、向腹侧延伸至底部的岛叶、背内侧核和丘脑枕核)反复出现显著结果,而其他结构(如杏仁核)则从未产生显著结果。经常发现左脑半球的结构比右脑半球的结构标记更强。(摘要截取自400字)