Boussaoud D, Jouffrais C, Bremmer F
Institut des Sciences Cognitives, Centre National de la Recherche Scientifique Unité Propre de Recherche 9075, Bron, France.
J Neurophysiol. 1998 Sep;80(3):1132-50. doi: 10.1152/jn.1998.80.3.1132.
Visual inputs to the brain are mapped in a retinocentric reference frame, but the motor system plans movements in a body-centered frame. This basic observation implies that the brain must transform target coordinates from one reference frame to another. Physiological studies revealed that the posterior parietal cortex may contribute a large part of such a transformation, but the question remains as to whether the premotor areas receive visual information, from the parietal cortex, readily coded in body-centered coordinates. To answer this question, we studied dorsal premotor cortex (PMd) neurons in two monkeys while they performed a conditional visuomotor task and maintained fixation at different gaze angles. Visual stimuli were presented on a video monitor, and the monkeys made limb movements on a panel of three touch pads located at the bottom of the monitor. A trial begins when the monkey puts its hand on the central pad. Then, later in the trial, a colored cue instructed a limb movement to the left touch pad if red or to the right one if green. The cues lasted for a variable delay, the instructed delay period, and their offset served as the go signal. The fixation spot was presented at the center of the screen or at one of four peripheral locations. Because the monkey's head was restrained, peripheral fixations caused a deviation of the eyes within the orbit, but for each fixation angle, the instructional cue was presented at nine locations with constant retinocentric coordinates. After the presentation of the instructional cue, 133 PMd cells displayed a phasic discharge (signal-related activity), 157 were tonically active during the instructed delay period (set-related or preparatory activity), and 104 were active after the go signal in relation to movement (movement-related activity). A large proportion of cells showed variations of the discharge rate in relation to limb movement direction, but only modest proportions were sensitive to the cue's location (signal, 43%; set, 34%; movement, 29%). More importantly, the activity of most neurons (signal, 74%; set, 79%; movement, 79%) varied significantly (analysis of variance, P < 0.05) with orbital eye position. A regression analysis showed that the neuronal activity varied linearly with eye position along the horizontal and vertical axes and can be approximated by a two-dimensional regression plane. These data provide evidence that eye position signals modulate the neuronal activity beyond sensory areas, including those involved in visually guided reaching limb movements. Further, they show that neuronal activity related to movement preparation and execution combines at least two directional parameters: arm movement direction and gaze direction in space. It is suggested that a substantial population of PMd cells codes limb movement direction in a head-centered reference frame.
大脑的视觉输入是以视网膜中心参考系进行映射的,但运动系统则是以身体中心参考系来规划运动的。这一基本观察结果表明,大脑必须将目标坐标从一个参考系转换到另一个参考系。生理学研究表明,后顶叶皮层可能在这种转换中发挥了很大作用,但问题仍然存在,即运动前区是否从顶叶皮层接收了以身体中心坐标形式轻松编码的视觉信息。为了回答这个问题,我们在两只猴子执行条件性视觉运动任务并在不同注视角度保持注视时,研究了背侧运动前皮层(PMd)神经元。视觉刺激在视频监视器上呈现,猴子在位于监视器底部的三个触摸板面板上进行肢体运动。当猴子将手放在中央触摸板上时,一次试验开始。然后,在试验后期,一个彩色提示指示如果是红色则肢体向左触摸板移动,如果是绿色则向右触摸板移动。提示持续可变的延迟时间,即指示延迟期,提示消失作为开始信号。注视点呈现在屏幕中心或四个周边位置之一。由于猴子的头部受到限制,周边注视会导致眼睛在眼眶内发生偏移,但对于每个注视角度,指示性提示在九个具有恒定视网膜中心坐标的位置呈现。在呈现指示性提示后,133个PMd细胞表现出相位放电(信号相关活动),157个在指示延迟期内持续活跃(设定相关或准备活动),104个在开始信号后与运动相关地活跃(运动相关活动)。很大一部分细胞的放电率随肢体运动方向而变化,但只有适度比例的细胞对提示的位置敏感(信号,43%;设定,34%;运动,29%)。更重要的是,大多数神经元的活动(信号,74%;设定,79%;运动,79%)随眼眶内眼睛位置有显著变化(方差分析,P < 0.05)。回归分析表明,神经元活动沿水平和垂直轴随眼睛位置呈线性变化,并且可以用二维回归平面近似。这些数据提供了证据,表明眼睛位置信号调节了包括参与视觉引导的伸手肢体运动的区域在内的感觉区域之外的神经元活动。此外,它们表明与运动准备和执行相关的神经元活动至少结合了两个方向参数:手臂运动方向和空间中的注视方向。有人提出,相当一部分PMd细胞以头部中心参考系编码肢体运动方向。