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Tecuapetla, F.

Publications and source records attributed to Tecuapetla, F..

2 recordsLinked to original sources

Basal ganglia output - entopeduncular nucleus - coding of contextual kinematics and reward in the freely moving mouse

The entopeduncular nucleus (EPN) is often termed as one of the output nuclei of the basal ganglia owing to their highly convergent anatomy. The rodent EPN has been implicated in reward and value coding whereas the primate analogue internal Globus Pallidus has been found to be modulated by some movements and in some circumstances. In this study we sought to understand how the rodent EPN might be coding kinematic, reward, and difficulty parameters, particularly during locomotion. Furthermore, we aimed to understand the level of movement representation: whole-body or specific body parts. To this end, mice were trained in a freely moving two-alternative forced choice task with two periods of displacement (return and go trajectories) and performed electrophysiological recordings together with video-based tracking. We found 1) robust reward coding but not difficulty. 2) Spatio-temporal variables better explain EPN activity during movement compared to kinematic variables, while both types of variables were more robustly represented in reward-related movement. 3) Reward sensitive units encode kinematics similarly to reward insensitive ones. 4) Population dynamics that best account for differences between these two periods of movement can be explained by allocentric references like distance to reward port. 5) The representation of paw and licks is not mutually exclusive, discarding a somatotopic muscle-level representation of movement in the EPN. Our data suggest that EPN activity represents movements and reward in a complex way: highly multiplexed, influenced by the objective of the displacement, where trajectories that lead to reward better represent spatial and kinematic variables. Interestingly, there are intertwining representations of whole-body movement kinematics with single paw and licking variables. Further, reward sensitive units encode kinematics similarly to reward insensitive ones, challenging the notion of distinct pathways for reward and movement processing. Significance StatementThe entopeduncular nucleus is one of the main outputs of the basal ganglia whose activity has been hypothesized to be inversely correlated with movement. This study examines motor and reward coding simultaneously, finding that besides the great level of multiplexing of these variables, spatio-temporal coding is better represented than kinematic coding. The level of movement representation seems to be greatly influenced by the goal of a movement, with spatially biased variables influencing the population dynamics of this nucleus. Further, we uncover the coexistence of EPN modulation by movement at different timescales and body parts. The simple overall activity of this output nucleus cannot explain kinematic coding, challenging leading theories of basal ganglia function.

neuroscience↗

Context dependent contributions of the direct and indirect pathways in the associative and sensorimotor striatum

To determine whether the contributions of striatal projection neurons from the direct (dSPNs) and indirect (iSPNs) pathways of the basal ganglia to action selection and locomotion can be generalized across the associative (DMS) and sensorimotor (DLS) striatum we compared the optogenetic activation or inhibition of these pathways on different tests. We show that self-modulation of dSPNs or iSPNs in either compartment has opposite contributions to real-time place preference, and to selecting an action in the DMS but not in the DLS. During reward seeking displacements, activation of either pathway in both compartments, or inhibition of dSPNs in the DMS slows movement. During spontaneous displacements, dSPNs activation showed opposing effects depending on the compartment modulated. Remarkably, inhibition of either pathway in the DLS decreases while only iSPNs inhibition in the DMS facilitates these displacements. These findings support a model of opposite, complementary and undescribed contributions of the striatal pathways depending on the compartment and context.

neuroscience↗