Kably B, Drew T
Centre Hospitalier, Hôpital des Spécialités, Service du Neurophysiologie, BP 6220 Rabat Institute, Morocco.
J Neurophysiol. 1998 Jul;80(1):406-24. doi: 10.1152/jn.1998.80.1.406.
We propose that the descending command from area 4 that is responsible, in part, for the change in limb trajectory required to step over an obstacle in one's path also plays a role in triggering the anticipatory postural modifications that accompany this movement. To test this hypothesis, we recorded the discharge characteristics of identified classes of corticofugal neurons in area 4 of the cat. Neurons were identified either as: pryamidal tract neurons (PTNs) if their axon projected to the caudal pyramidal tract (PT) but not to the pontomedullary reticular formation (PMRF); as corticoreticular neurons (CRNs) if their axon projected to the PMRF but not to the PT; and as PTN/CRNs if their axon projected to both structures. Altogether, the discharge properties of 212 corticofugal neurons (109 PTNs, 66 PTN/CRNs, and 37 CRNs) within area 4 were recorded during voluntary gait modifications. Neurons in all three classes showed increases in their discharge frequency during locomotion and included groups that increased their discharge either during the swing phase of the modified step, during the subsequent stance phase, or in the stance phase of the cycle preceding the step over the obstacle. A slightly higher percentage of CRNs (39%) discharged in the stance phase prior to the gait modification than did the PTNs or PTN/CRNs (20% and 17% respectively). In 37 electrode penetrations, we were able to record clusters of 3 or more neurons within 500 micro(m) of each other. In most cases, PTN/CRNs recorded in close proximity to PTNs had similar receptive fields and discharged in a similar, but not identical, manner during the gait modifications. Compared with adjacent PTNs, CRNs normally showed a more variable pattern of activity and frequently discharged earlier in the step cycle than did the PTNs or PTN/CRNs. We interpret the results as providing support for the original hypothesis. We suggest that the collateral branches to the PMRF from corticofugal neurons with axons that continue at least as far as the caudal PT provide a signal that could be used to trigger dynamic postural responses that are appropriately organized and scaled for the movements that are being undertaken. We suggest that the more variable and earlier discharge activity observed in CRNs might be used to modify the postural support on which the movements and the dynamic postural adjustments are superimposed.
我们提出,来自4区的下行指令在一定程度上负责改变肢体轨迹以跨过路径中的障碍物,它在触发伴随该运动的预期姿势调整中也发挥作用。为了验证这一假设,我们记录了猫4区中已识别的几类皮质传出神经元的放电特性。神经元被识别为:如果其轴突投射到尾侧锥体束(PT)但不投射到脑桥延髓网状结构(PMRF),则为锥体束神经元(PTN);如果其轴突投射到PMRF但不投射到PT,则为皮质网状神经元(CRN);如果其轴突投射到这两个结构,则为PTN/CRN。在自愿改变步态期间,共记录了4区内212个皮质传出神经元(109个PTN、66个PTN/CRN和37个CRN)的放电特性。所有这三类神经元在运动期间其放电频率均增加,并且包括在修改步骤的摆动阶段、随后的站立阶段或跨过障碍物之前的周期的站立阶段放电增加的组。在步态改变之前的站立阶段放电的CRN百分比(39%)略高于PTN或PTN/CRN(分别为20%和17%)。在37个电极穿刺中,我们能够记录到彼此距离在500微米内的3个或更多神经元的集群。在大多数情况下,与PTN紧邻记录的PTN/CRN具有相似的感受野,并且在步态改变期间以相似但不完全相同的方式放电。与相邻的PTN相比,CRN通常表现出更可变的活动模式,并且在步周期中比PTN或PTN/CRN更早放电。我们将这些结果解释为支持了最初的假设。我们认为,轴突至少延伸到尾侧PT的皮质传出神经元向PMRF发出的侧支提供了一个信号,该信号可用于触发动态姿势反应,这些反应针对正在进行的运动进行了适当的组织和调整。我们认为,在CRN中观察到的更可变和更早的放电活动可能用于修改运动和动态姿势调整所叠加的姿势支撑。