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Francis, J. T.

Publications and source records attributed to Francis, J. T..

3 recordsLinked to original sources

Motor Cortex Encodes A Value Function Consistent With Reinforcement Learning

Temporal difference reinforcement learning (TDRL) accurately models associative learning observed in animals, where they learn to associate outcome predicting environmental states, termed conditioned stimuli (CS), with the value of outcomes, such as rewards, termed unconditioned stimuli (US). A component of TDRL is the value function, which captures the expected cumulative future reward from a given state. The value function can be modified by changes in the animals knowledge, such as by the predictability of its environment. Here we show that primary motor cortical (M1) neurodynamics reflect a TD learning process, encoding a state value function and reward prediction error in line with TDRL. M1 responds to the delivery of reward, and shifts its value related response earlier in a trial, becoming predictive of an expected reward, when reward is predictable due to a CS. This is observed in tasks performed manually or observed passively, as well as in tasks without an explicit CS predicting reward, but simply with a predictable temporal structure, that is a predictable environment. M1 also encodes the expected reward value associated with a set of CS in a multiple reward level CS-US task. Here we extend the Microstimulus TDRL model, reported to accurately capture RL related dopaminergic activity, to account for M1 reward related neural activity in a multitude of tasks.\n\nSignificance statementThere is a great deal of agreement between aspects of temporal difference reinforcement learning (TDRL) models and neural activity in dopaminergic brain centers. Dopamine is know to be necessary for sensorimotor learning induced synaptic plasticity in the motor cortex (M1), and thus one might expect to see the hallmarks of TDRL in M1, which we show here in the form of a state value function and reward prediction error during. We see these hallmarks even when a conditioned stimulus is not available, but the environment is predictable, during manual tasks with agency, as well as observational tasks without agency. This information has implications towards autonomously updating brain machine interfaces as others and we have proposed and published on.

neuroscience

Near Perfect Neural Critic from Motor Cortical Activity Toward an Autonomously Updating Brain Machine Interface

We are developing an autonomously updating brain machine interface (BMI) utilizing reinforcement learning principles. One aspect of this system is a neural critic that determines reward expectations from neural activity. This critic is then used to update a BMI decoder towards an improved performance from the users perspective. Here we demonstrate the ability of a neural critic to classify trial reward value given activity from the primary motor cortex (M1), using neural features from single/multi units (SU/MU), and local field potentials (LFPs) with prediction accuracies up to 97% correct. A nonhuman primate subject conducted a cued center out reaching task, either manually, or observationally. The cue indicated the reward value of a trial. Features such as power spectral density (PSD) of the LFPs and spike-field coherence (SFC) between SU/MU and corresponding LFPs were calculated and used as inputs to several classifiers. We conclude that hybrid features of PSD and SFC show higher classification performance than PSD or SFC alone (accuracy was 92% for manual tasks, and 97% for observational). In the future, we will employ these hybrid features towards our autonomously updating BMI.

neuroscience

Layer-Specific Molecular Dynamics of PKMζ in Sensorimotor Cortex During Acquisition and Storage of Procedural Memory

Procedural memories, such as for riding a bicycle, can be maintained without practice for long periods of time and are thought to be supported by the persistent reorganization of sensorimotor cortices (S1/M1). Whereas enhanced synaptic strength and structural changes accompany the learning of motor tasks, the persistent molecular modifications that store long-term procedural memories within specific layers of sensorimotor cortex have not been identified. The persistent increase in the autonomously active, atypical PKC isoform, PKM{zeta}, is a putative molecular mechanism for maintaining enhanced synaptic strength during long-term potentiation (LTP) and several forms of long-term memory. Here we examine whether persistent increases in PKM{zeta} store long-term memory for a reaching task in rat sensorimotor cortex that could reveal the sites of procedural memory storage. Perturbing PKM{zeta} synthesis with PKM{zeta} -antisense oligodeoxynucleotides or blocking atypical PKC activity with zeta inhibitory peptide (ZIP) in S1/M1 disrupts and erases the maintenance of long-term motor memories. Only memories that are maintained without daily reinforcement are affected, indicating atypical PKCs (via ZIP) and PKM{zeta} specifically (via antisense) stores consolidated long-term procedural memories. Analysis of changes in the amount of PKM{zeta} in S1/M1 reveals PKM{zeta} increases in layers II/III and V of both S1 and M1 cortices as performance improves to an asymptote during training. After storage for 1 month without reinforcement, the increase in M1 layer V but not other layers persists without decrement. Thus, the sustained increases in PKM{zeta} reveal that the persistent molecular changes storing long-term procedural memory are localized to the descending output layer of primary motor cortex.

neuroscience