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Marino, P. J.

Publications and source records attributed to Marino, P. J..

4 recordsLinked to original sources

Reward influences movement vigor through multiple motor cortical mechanisms

The prospect of greater rewards often invigorates movements. What neural mechanisms support this increase of movement vigor for greater rewards? We had three rhesus monkeys perform reaching movements to targets worth different magnitudes of reward. We recorded neural population activity from primary motor and dorsal premotor cortex, brain areas at the output of cortical processing for voluntary movements, and asked how neural activity mediated the translation of reward into increased vigor. We identified features of neural activity during movement preparation, initiation, and execution that were both correlated with vigor and modulated by reward. We also found that the neural metrics that correlate with different aspects of movement vigor exhibit only limited correlation with one another, suggesting that there are multiple mechanisms through which reward modulates vigor. Finally, we note that the majority of rewards modulation of motor cortical activity cannot be accounted for by reward-mediated vigor differences in behavior, indicating that reward modulations within motor cortex may serve roles in addition to affecting vigor. Overall, our results provide insight into the neural mechanisms that link reward-driven motivation to the modulation of the details of movement.

neuroscience↗

A posture subspace in primary motor cortex

To generate movements, the brain must combine information about movement goal and body posture. Motor cortex (M1) is a key node for the convergence of these information streams. How are posture and goal information organized within M1s activity to permit the flexible generation of movement commands? To answer this question, we recorded M1 activity while monkeys performed a variety of tasks with the forearm in a range of postures. We found that posture- and goal-related components of neural population activity were separable and resided in nearly orthogonal subspaces. The posture subspace was stable across tasks. Within each task, neural trajectories for each goal had similar shapes across postures. Our results reveal a simpler organization of posture information in M1 than previously recognized. The compartmentalization of posture and goal information might allow the two to be flexibly combined in the service of our broad repertoire of actions.

neuroscience↗

Dynamical constraints on neural population activity

The manner in which neural activity unfolds over time is thought to be central to sensory, motor, and cognitive functions in the brain. Network models have long posited that the brains computations involve time courses of activity that are shaped by the underlying network. A prediction from this view is that the activity time courses should be difficult to violate. We leveraged a brain-computer interface (BCI) to challenge monkeys to violate the naturally-occurring time courses of neural population activity that we observed in motor cortex. This included challenging animals to traverse the natural time course of neural activity in a time-reversed manner. Animals were unable to violate the natural time courses of neural activity when directly challenged to do so. These results provide empirical support for the view that activity time courses observed in the brain indeed reflect the underlying network-level computational mechanisms that they are believed to implement.

neuroscience↗

A neural basis of choking under pressure

Incentives tend to drive improvements in performance. But when incentives get too high, we can "choke under pressure" and underperform when it matters most. What neural processes might lead to choking under pressure? We studied Rhesus monkeys performing a challenging reaching task in which they underperform when an unusually large "jackpot" reward is at stake. We observed a collapse in neural information about upcoming movements for jackpot rewards: in the motor cortex, neural planning signals became less distinguishable for different reach directions when a jackpot reward was made available. We conclude that neural signals of reward and motor planning interact in the motor cortex in a manner that can explain why we choke under pressure. One-Sentence SummaryIn response to exceptionally large reward cues, animals can "choke under pressure", and this corresponds to a collapse in the neural information about upcoming movements.

neuroscience↗