Cromer Jason A, Waitzman David M
University of Connecticut Health Center, Department of Neurology, Farmington, Connecticut 06030, USA.
J Neurophysiol. 2007 Aug;98(2):835-50. doi: 10.1152/jn.00308.2007. Epub 2007 May 30.
The oculomotor system must convert signals representing the target of an intended eye movement into appropriate input to drive the individual extraocular muscles. Neural models propose that this transformation may involve either a decomposition of the intended eye displacement signal into horizontal and vertical components or an implicit process whereby component signals do not predominate until the level of the motor neurons. Thus decomposition models predict that premotor neurons should primarily encode component signals while implicit models predict encoding of off-cardinal optimal directions by premotor neurons. The central mesencephalic reticular formation (cMRF) and paramedian pontine reticular formation (PPRF) are two brain stem regions that likely participate in the development of motor activity since both structures are anatomically connected to nuclei that encode movement goal (superior colliculus) and generate horizontal eye movements (abducens nucleus). We compared cMRF and PPRF neurons and found they had similar relationships to saccade dynamics, latencies, and movement fields. Typically, the direction preference of these premotor neurons was horizontal, suggesting they were related to saccade components. To confirm this supposition, we studied the neurons during a series of oblique saccades that caused "component stretching" and thus allowed the vectorial (overall) saccade velocity to be dissociated from horizontal component velocity. The majority of cMRF and PPRF neurons encoded component velocity across all saccades, supporting decomposition models that suggest horizontal and vertical signals are generated before the level of the motoneurons. However, we also found novel vectorial eye velocity encoding neurons that may have important implications for saccade control.
动眼系统必须将代表预期眼球运动目标的信号转换为适当的输入,以驱动各个眼外肌。神经模型提出,这种转换可能涉及将预期眼球位移信号分解为水平和垂直分量,或者是一个隐式过程,即分量信号直到运动神经元水平才占主导地位。因此,分解模型预测,运动前神经元应主要编码分量信号,而隐式模型预测运动前神经元对非主要最优方向进行编码。中脑中央网状结构(cMRF)和脑桥旁正中网状结构(PPRF)是两个脑干区域,它们可能参与运动活动的发展,因为这两个结构在解剖学上都与编码运动目标的核(上丘)和产生水平眼球运动的核(展神经核)相连。我们比较了cMRF和PPRF神经元,发现它们与扫视动力学、潜伏期和运动野具有相似的关系。通常,这些运动前神经元的方向偏好是水平的,这表明它们与扫视分量有关。为了证实这一假设,我们在一系列倾斜扫视过程中研究了这些神经元,这些扫视导致了“分量拉伸”,从而使矢量(整体)扫视速度与水平分量速度分离。大多数cMRF和PPRF神经元在所有扫视过程中都编码分量速度,这支持了分解模型,即水平和垂直信号在运动神经元水平之前就已产生。然而,我们还发现了新的矢量眼速度编码神经元,它们可能对扫视控制具有重要意义。