The Role of the Dorsal Premotor and Superior Parietal Cortices in Decoupled Visuomotor Transformations

In order to successfully interact with objects located within our environment, the brain must be capable of combining visual information with the appropriate felt limb position (i.e. proprioception) in order compute an appropriate coordinated muscle plan for accurate motor control. Eye-hand coordination is essential to our independence as a species and relies heavily on the reciprocally-connected regions of the parieto-frontal reach network. The dorsal premotor cortex (PMd) and the superior parietal lobule (SPL) remain prime candidates within this network for controlling the transformations required during visually-guided reaching movements. Our brains are primed to reach directly towards a viewed object, a situation that has been termed a “standard” or coupled reach. Such direct eye-hand coordination is common across species and is crucial for basic survival. Humans, however, have developed the capacity for tool-use and thus have learned to interact indirectly with an object. In such “non-standard” or decoupled situations, the directions of gaze and arm movement have been spatially decoupled and rely on both the implementation of a cognitive rule and on online feedback of the decoupled limb. The studies included within this dissertation were designed to further characterize the role of PMd and SPL during situations in which when a reach requires a spatial transformation between the actions of the eyes and the hand. More specifically, we were interested in examining whether regions within PMd (PMdr, PMdc) and SPL (PEc, MIP) responded differently during coupled versus decoupled visuomotor transformations. To address the relative contribution of these various cortical regions during decoupled reaching movements, we trained two female rhesus macaques on both coupled and decoupled visually-guided reaching tasks. We recorded the neural activity (single units and local field potentials) within each region while the animals performed each condition. We found that two separate networks emerged each contributing in a distinct ways to the performance of coupled versus decoupled eye-hand reaches. While PMdr and PEc showed enhanced activity during decoupled reach conditions, PMdc and MIP were more enhanced during coupled reaches. Taken together, these data presented here provide further evidence for the existence of alternate task-dependent neural pathways for visuomotor integration.