University of Parma, Department of Neuroscience, via Volturno 39/E, 43100 Parma, Italy.
Neuroimage. 2013 Jan 1;64:425-36. doi: 10.1016/j.neuroimage.2012.09.026. Epub 2012 Sep 17.
While there have been several studies investigating the neural correlates of action observation associated with hand grasping movements, comparatively little is known about the neural bases of observation of reaching movements. In two experiments, using functional magnetic resonance imaging (fMRI), we defined the cortical areas encoding reaching movements and assessed their sensitivity to biological motion and to movement velocity. In the first experiment, participants observed video-clips showing either a biological effector (an arm) or a non-biological object (rolling cylinder) reaching toward a target with a biological and a non-biological motion, respectively. In the second experiment, participants observed video-clips showing either a biological effector (an arm) or a non-biological object (an arrow) reaching toward a target with the same biological motion profiles. The results of the two experiments revealed activation of superior parietal and dorsal premotor sites during observation of the biological motion only, independent of whether it was performed by a biological effector (reaching arm) or a non-biological object (reaching arrow). These areas were not activated when participants observed the non-biological movement (rolling cylinder). To assess the responsiveness of parietal and frontal sites to movement velocity, the fMRI repetition-suppression (RS) technique was used, in which movement was shown with same or different velocities between consecutive videos, and observation of identical stimuli was contrasted with observation of different stimuli. Regions of interest were defined in the parietal and frontal cortices, and their response to stimulus repetition was analyzed (same vs. different velocities). The results showed an RS effect for velocity only during the observation of movements performed by the biological effector and not by the non-biological object. These data indicate that dorsal premotor and superior parietal areas represent a neural substrate involved in the encoding of reaching movements and that their responsiveness to movement velocity of a biological effector could be instrumental to the discrimination of movements performed by others.
虽然已经有几项研究调查了与手抓握运动相关的动作观察的神经相关性,但对于观察伸手运动的神经基础知之甚少。在两项实验中,我们使用功能磁共振成像(fMRI)定义了编码伸手运动的皮质区域,并评估了它们对生物运动和运动速度的敏感性。在第一个实验中,参与者观察了视频片段,这些片段分别显示了一个生物效应器(手臂)或一个非生物物体(滚动圆柱体)以生物和非生物运动分别伸向目标。在第二个实验中,参与者观察了视频片段,这些片段分别显示了一个生物效应器(手臂)或一个非生物物体(箭头)以相同的生物运动模式伸向目标。两个实验的结果显示,在观察生物运动时,只有 Superior Parietal 和 Dorsal Premotor 区域被激活,而不管它是由生物效应器(伸手臂)还是非生物物体(伸手箭头)执行的。当参与者观察非生物运动(滚动圆柱体)时,这些区域不会被激活。为了评估顶叶和额叶区域对运动速度的反应性,使用 fMRI 重复抑制(RS)技术,在该技术中,在连续的视频中显示相同或不同的速度,并且观察相同的刺激与观察不同的刺激进行对比。在顶叶和额叶皮质中定义了感兴趣区域,并分析了它们对刺激重复的反应(相同速度与不同速度)。结果表明,只有在观察生物效应器执行的运动时,才会出现速度的 RS 效应,而不是非生物物体。这些数据表明,背侧运动前区和顶叶区代表了参与编码伸手运动的神经基质,并且它们对生物效应器运动速度的反应性可能有助于区分他人执行的运动。