Publications by authors named "Niceto Luque"

Robots have to adjust their motor behavior to changing environments and variable task requirements to successfully operate in the real world and physically interact with humans. Thus, robotics strives to enable a broad spectrum of adjustable motor behavior, aiming to mimic the human ability to function in unstructured scenarios. In humans, motor behavior arises from the integrative action of the central nervous system and body biomechanics; motion must be understood from a neuromechanics perspective.

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Complex interactions between brain regions and the spinal cord (SC) govern body motion, which is ultimately driven by muscle activation. Motor planning or learning are mainly conducted at higher brain regions, whilst the SC acts as a brain-muscle gateway and as a motor control centre providing fast reflexes and muscle activity regulation. Thus, higher brain areas need to cope with the SC as an inherent and evolutionary older part of the body dynamics.

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Collaborative robots, or cobots, are designed to work alongside humans and to alleviate their physical burdens, such as lifting heavy objects or performing tedious tasks. Ensuring the safety of human-robot interaction (HRI) is paramount for effective collaboration. To achieve this, it is essential to have a reliable dynamic model of the cobot that enables the implementation of torque control strategies.

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The inferior olivary (IO) nucleus makes up the signal gateway for several organs to the cerebellar cortex. Located within the sensory-motor-cerebellum pathway, the IO axons, i.e.

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The vestibulo-ocular reflex (VOR) stabilizes vision during head motion. Age-related changes of vestibular neuroanatomical properties predict a linear decay of VOR function. Nonetheless, human epidemiological data show a stable VOR function across the life span.

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The presence of computation and transmission-variable time delays within a robotic control loop is a major cause of instability, hindering safe human-robot interaction (HRI) under these circumstances. Classical control theory has been adapted to counteract the presence of such variable delays; however, the solutions provided to date cannot cope with HRI robotics inherent features. The highly nonlinear dynamics of HRI cobots (robots intended for human interaction in collaborative tasks), together with the growing use of flexible joints and elastic materials providing passive compliance, prevent traditional control solutions from being applied.

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The work presented here is a novel biological approach for the compliant control of a robotic arm in real time (RT). We integrate a spiking cerebellar network at the core of a feedback control loop performing torque-driven control. The spiking cerebellar controller provides torque commands allowing for accurate and coordinated arm movements.

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Cerebellar Purkinje cells mediate accurate eye movement coordination. However, it remains unclear how oculomotor adaptation depends on the interplay between the characteristic Purkinje cell response patterns, namely tonic, bursting, and spike pauses. Here, a spiking cerebellar model assesses the role of Purkinje cell firing patterns in vestibular ocular reflex (VOR) adaptation.

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Article Synopsis
  • A spiking cerebellar model is integrated into a real-time control system for the iCub robot, enabling it to perform vestibulo-ocular reflex (VOR) tasks.
  • The system experiences nondeterministic computation times due to neural activity, prompting the use of a real-time supervisor that manages simulation speed and neural operations to maintain effective robot functionality.
  • The research explores how the interplay between cerebellar neural dynamics and plasticity contributes to motor adaptation during VOR tasks, emphasizing the importance of a two-stage learning process.
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Supervised learning has long been attributed to several feed-forward neural circuits within the brain, with particular attention being paid to the cerebellar granular layer. The focus of this study is to evaluate the input activity representation of these feed-forward neural networks. The activity of cerebellar granule cells is conveyed by parallel fibers and translated into Purkinje cell activity, which constitutes the sole output of the cerebellar cortex.

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Article Synopsis
  • This pertains to a correction made in a specific article found on page 7 of volume 11.
  • It includes reference number PMID: 28223930 for additional context.
  • The specifics of the correction are not detailed in this synopsis.
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Modeling and simulating the neural structures which make up our central neural system is instrumental for deciphering the computational neural cues beneath. Higher levels of biological plausibility usually impose higher levels of complexity in mathematical modeling, from neural to behavioral levels. This paper focuses on overcoming the simulation problems (accuracy and performance) derived from using higher levels of mathematical complexity at a neural level.

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The cerebellar microcircuit has been the work bench for theoretical and computational modeling since the beginning of neuroscientific research. The regular neural architecture of the cerebellum inspired different solutions to the long-standing issue of how its circuitry could control motor learning and coordination. Originally, the cerebellar network was modeled using a statistical-topological approach that was later extended by considering the geometrical organization of local microcircuits.

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The majority of operations carried out by the brain require learning complex signal patterns for future recognition, retrieval and reuse. Although learning is thought to depend on multiple forms of long-term synaptic plasticity, the way this latter contributes to pattern recognition is still poorly understood. Here, we have used a simple model of afferent excitatory neurons and interneurons with lateral inhibition, reproducing a network topology found in many brain areas from the cerebellum to cortical columns.

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Article Synopsis
  • Deep cerebellar nuclei neurons integrate inhibitory signals from Purkinje cells and excitatory signals from mossy fibers to support precise motor control and adaptive learning.
  • The study introduces a new spiking model that highlights the dual role of deep cerebellar nuclei in gain adaptation and memory consolidation.
  • By utilizing both excitatory and inhibitory spike-timing-dependent plasticity (STDP) mechanisms, the cerebellum can adjust synaptic memories and optimize output firing rates for better motor function.
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Article Synopsis
  • The study aimed to create a realistic cerebellar model using artificial spiking neural networks to simulate motor tasks, focusing on associative learning and extinction across multiple sessions.
  • Evolutionary algorithms were employed to fine-tune the parameters of the cerebellar microcircuit, comparing two models: one with only cortical plasticity and another incorporating additional nuclear plasticity sites, both demonstrating human-like behavioral responses in eye blink conditioning.
  • Results indicated that the model with distributed plasticity exhibited superior learning capabilities, resulting in faster and more stable acquisition and reacquisition of conditioned responses, suggesting the importance of multiple neural mechanisms in complex learning processes.
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The cerebellum is involved in learning and memory of sensory motor skills. However, the way this process takes place in local microcircuits is still unclear. The initial proposal, casted into the Motor Learning Theory, suggested that learning had to occur at the parallel fiber-Purkinje cell synapse under supervision of climbing fibers.

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Article Synopsis
  • The cerebellum plays a key role in associative learning and fine motor control, contributing to a better understanding of how our brain processes movement and learning.
  • Researchers have created a realistic cerebellar spiking neural network (SNN) that interacts with a robot to tackle various sensorimotor tasks, demonstrating how these neural processes can drive complex behaviors.
  • The SNN successfully adapts its motor responses in real-time by adjusting timing and gain, mimicking human learning in a dynamic environment and showing effective robustness and generalizability across different tasks.
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The cerebellum is known to play a critical role in learning relevant patterns of activity for adaptive motor control, but the underlying network mechanisms are only partly understood. The classical long-term synaptic plasticity between parallel fibers (PFs) and Purkinje cells (PCs), which is driven by the inferior olive (IO), can only account for limited aspects of learning. Recently, the role of additional forms of plasticity in the granular layer, molecular layer and deep cerebellar nuclei (DCN) has been considered.

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Time-driven simulation methods in traditional CPU architectures perform well and precisely when simulating small-scale spiking neural networks. Nevertheless, they still have drawbacks when simulating large-scale systems. Conversely, event-driven simulation methods in CPUs and time-driven simulation methods in graphic processing units (GPUs) can outperform CPU time-driven methods under certain conditions.

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Adaptable gain regulation is at the core of the forward controller operation performed by the cerebro-cerebellar loops and it allows the intensity of motor acts to be finely tuned in a predictive manner. In order to learn and store information about body-object dynamics and to generate an internal model of movement, the cerebellum is thought to employ long-term synaptic plasticity. LTD at the PF-PC synapse has classically been assumed to subserve this function (Marr, 1969).

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The cerebellum is thought to mediate sensorimotor adaptation through the acquisition of internal models of the body-environment interaction. These representations can be of two types, identified as forward and inverse models. The first predicts the sensory consequences of actions, while the second provides the correct commands to achieve desired state transitions.

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In this work, a basic cerebellar neural layer and a machine learning engine are embedded in a recurrent loop which avoids dealing with the motor error or distal error problem. The presented approach learns the motor control based on available sensor error estimates (position, velocity, and acceleration) without explicitly knowing the motor errors. The paper focuses on how to decompose the input into different components in order to facilitate the learning process using an automatic incremental learning model (locally weighted projection regression (LWPR) algorithm).

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This study proposes an adaptive control architecture based on an accurate regression method called Locally Weighted Projection Regression (LWPR) and on a bio-inspired module, such as a cerebellar-like engine. This hybrid architecture takes full advantage of the machine learning module (LWPR kernel) to abstract an optimized representation of the sensorimotor space while the cerebellar component integrates this to generate corrective terms in the framework of a control task. Furthermore, we illustrate how the use of a simple adaptive error feedback term allows to use the proposed architecture even in the absence of an accurate analytic reference model.

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