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., climbing fibres (CFs), massively synapse onto the cerebellar Purkinje cells (PCs) regulating motor learning whilst the olivary nucleus receives negative feedback through the GABAergic nucleo-olivary​ (NO) pathway. The NO pathway regulates the electrical coupling (EC) amongst the olivary cells thus facilitating synchrony and timing. However, the involvement of this EC regulation on cerebellar adaptive behaviour is still under debate. In our study we have used a spiking cerebellar model to assess the role of the NO pathway in regulating vestibulo-ocular-reflex (VOR) adaptation. The model incorporates spike-based synaptic plasticity at multiple cerebellar sites and an electrically-coupled olivary system. The olivary system plays a central role in regulating the CF spike-firing patterns that drive the PCs, whose axons ultimately shape the cerebellar output. Our results suggest that a systematic GABAergic NO deactivation decreases the spatio-temporal complexity of the IO firing patterns thereby worsening the temporal resolution of the olivary system. Conversely, properly coded IO spatio-temporal firing patterns, thanks to NO modulation, finely shape the balance between long-term depression and potentiation, which optimises VOR adaptation. Significantly, the NO connectivity pattern constrained to the same micro-zone helps maintain the spatio-temporal complexity of the IO firing patterns through time. Moreover, the temporal alignment between the latencies found in the NO fibres and the sensory-motor pathway delay appears to be crucial for facilitating the VOR. When we consider all the above points we believe that these results predict that the NO pathway is instrumental in modulating the olivary coupling and relevant to VOR adaptation.

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. In this study, we model cerebellum-dependent VOR adaptation to relate structural and functional changes throughout aging. We consider three neurosynaptic factors that may codetermine VOR adaptation during aging: the electrical coupling of inferior olive neurons, the long-term spike timing-dependent plasticity at parallel fiber - Purkinje cell synapses and mossy fiber - medial vestibular nuclei synapses, and the intrinsic plasticity of Purkinje cell synapses Our cross-sectional aging analyses suggest that long-term plasticity acts as a global homeostatic mechanism that underpins the stable temporal profile of VOR function. The results also suggest that the intrinsic plasticity of Purkinje cell synapses operates as a local homeostatic mechanism that further sustains the VOR at older ages. Importantly, the computational epidemiology approach presented in this study allows discrepancies among human cross-sectional studies to be understood in terms of interindividual variability in older individuals. Finally, our longitudinal aging simulations show that the amount of residual fibers coding for the peak and trough of the VOR cycle constitutes a predictive hallmark of VOR trajectories over a lifetime.

Hippocampal place cells and entorhinal grid cells are thought to form a representation of space by integrating internal and external sensory cues. Experimental data show that different subsets of place cells are controlled by vision, self-motion or a combination of both. Moreover, recent studies in environments with a high degree of visual aliasing suggest that a continuous interaction between place cells and grid cells can result in a deformation of hexagonal grids or in a progressive loss of visual cue control over grid fields. The computational nature of such a bidirectional interaction remains unclear. In this work we present a neural network model of the dynamic interaction between place cells and grid cells within the entorhinal-hippocampal processing loop. The model was tested in two recent experimental paradigms involving environments with visually similar compartments that provided conflicting evidence about visual cue control over self-motion-based spatial codes. Analysis of the model behavior suggests that the strength of entorhinal-hippocampal dynamical loop is the key parameter governing differential cue control in multi-compartment environments. Moreover, construction of separate spatial representations of visually identical compartments required a progressive weakening of visual cue control over place fields in favor of self-motion based mechanisms. More generally our results suggest a functional segregation between plastic and dynamic processes in hippocampal processing.

We embed a spiking cerebellar model within an adaptive real-time (RT) control loop that is able to operate a real robotic body (iCub) when performing different vestibulo-ocular reflex (VOR) tasks. The spiking neural network computation, including event- and time-driven neural dynamics, neural activity, and spike-timing dependent plasticity (STDP) mechanisms, leads to a nondeterministic computation time caused by the neural activity volleys encountered during cerebellar simulation. This nondeterministic computation time motivates the integration of an RT supervisor module that is able to ensure a well-orchestrated neural computation time and robot operation. Actually, our neurorobotic experimental setup (VOR) benefits from the biological sensory motor delay between the cerebellum and the body to buffer the computational overloads as well as providing flexibility in adjusting the neural computation time and RT operation. The RT supervisor module provides for incremental countermeasures that dynamically slow down or speed up the cerebellar simulation by either halting the simulation or disabling certain neural computation features (i.e., STDP mechanisms, spike propagation, and neural updates) to cope with the RT constraints imposed by the real robot operation. This neurorobotic experimental setup is applied to different horizontal and vertical VOR adaptive tasks that are widely used by the neuroscientific community to address cerebellar functioning. We aim to elucidate the manner in which the combination of the cerebellar neural substrate and the distributed plasticity shapes the cerebellar neural activity to mediate motor adaptation. This paper underlies the need for a two-stage learning process to facilitate VOR acquisition.

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. The model captures the cerebellar microcircuit properties and it incorporates spike-based synaptic plasticity at multiple cerebellar sites. A detailed Purkinje cell model reproduces the three spike-firing patterns that are shown to regulate the cerebellar output. Our results suggest that pauses following Purkinje complex spikes (bursts) encode transient disinhibition of target medial vestibular nuclei, critically gating the vestibular signals conveyed by mossy fibres. This gating mechanism accounts for early and coarse VOR acquisition, prior to the late reflex consolidation. In addition, properly timed and sized Purkinje cell bursts allow the ratio between long-term depression and potentiation (LTD/LTP) to be finely shaped at mossy fibre-medial vestibular nuclei synapses, which optimises VOR consolidation. Tonic Purkinje cell firing maintains the consolidated VOR through time. Importantly, pauses are crucial to facilitate VOR phase-reversal learning, by reshaping previously learnt synaptic weight distributions. Altogether, these results predict that Purkinje spike burst-pause dynamics are instrumental to VOR learning and reversal adaptation.

Studying and understanding the computational primitives of our neural system requires for a diverse and complementary set of techniques. In this work, we use the Neuro-robotic Platform (NRP)to evaluate the vestibulo ocular cerebellar adaptatIon (Vestibulo-ocular reflex, VOR)mediated by two STDP mechanisms located at the cerebellar molecular layer and the vestibular nuclei respectively. This simulation study adopts an experimental setup (rotatory VOR)widely used by neuroscientists to better understand the contribution of certain specific cerebellar properties (i.e. distributed STDP, neural properties, coding cerebellar topology, etc.)to r-VOR adaptation. The work proposes and describes an embodiment solution for which we endow a simulated humanoid robot (iCub)with a spiking cerebellar model by means of the NRP, and we face the humanoid to an r-VOR task. The results validate the adaptive capabilities of the spiking cerebellar model (with STDP)in a perception-action closed-loop (r- VOR)causing the simulated iCub robot to mimic a human behavior.

We set forth an information-theoretical measure to quantify neurotransmission reliability while taking into full account the metrical properties of the spike train space. This parametric information analysis relies on similarity measures induced by the metrical relations between neural responses as spikes flow in. Thus, in order to assess the entropy, the conditional entropy, and the overall information transfer, this method does not require any a priori decoding algorithm to partition the space into equivalence classes. It therefore allows the optimal parameters of a class of distances to be determined with respect to information transmission. To validate the proposed information-theoretical approach, we study precise temporal decoding of human somatosensory signals recorded using microneurography experiments. For this analysis, we employ a similarity measure based on the Victor-Purpura spike train metrics. We show that with appropriate parameters of this distance, the relative spike times of the mechanoreceptors' responses convey enough information to perform optimal discrimination--defined as maximum metrical information and zero conditional entropy--of 81 distinct stimuli within 40 ms of the first afferent spike. The proposed information-theoretical measure proves to be a suitable generalization of Shannon mutual information in order to consider the metrics of temporal codes explicitly. It allows neurotransmission reliability to be assessed in the presence of large spike train spaces (e.g., neural population codes) with high temporal precision.

The interplay between hippocampus and prefrontal cortex (PFC) is fundamental to spatial cognition. Complementing hippocampal place coding, prefrontal representations provide more abstract and hierarchically organized memories suitable for decision making. We model a prefrontal network mediating distributed information processing for spatial learning and action planning. Specific connectivity and synaptic adaptation principles shape the recurrent dynamics of the network arranged in cortical minicolumns. We show how the PFC columnar organization is suitable for learning sparse topological-metrical representations from redundant hippocampal inputs. The recurrent nature of the network supports multilevel spatial processing, allowing structural features of the environment to be encoded. An activation diffusion mechanism spreads the neural activity through the column population leading to trajectory planning. The model provides a functional framework for interpreting the activity of PFC neurons recorded during navigation tasks. We illustrate the link from single unit activity to behavioral responses. The results suggest plausible neural mechanisms subserving the cognitive "insight" capability originally attributed to rodents by Tolman & Honzik. Our time course analysis of neural responses shows how the interaction between hippocampus and PFC can yield the encoding of manifold information pertinent to spatial planning, including prospective coding and distance-to-goal correlates.

A framework to discriminate tactile stimuli delivered to an artificial touch sensor is presented. Following a neuromimetic approach, we encode the signals from a 24-capacitive sensor fingertip into spiking activity through a network of leaky integrate-and-fire neurons. The activity resulting from the stimulation of the touch sensor through Braille-like dot patterns is then analysed by means of a newly defined Information measure which explicitly takes into consideration the metrics of the spike train space. Results show that an optimal discrimination of the entire set of 26 stimuli (i.e. 100% correct classification) is reached early after the stimulus onset. Interestingly, the method proves to be effective with both statically and dynamically delivered stimulation which are hard to decode because of the similarity between encoded firing activity given to the proximity of the patterns presented. The decoding analysis allowed us to corroborate the working hypothesis that human tactile discrimination relies on optimal encoding/decoding processes already at the level of the primary stage neurons in the somatosensory pathway.

A nerve cell receives multiple inputs from upstream neurons by way of its synapses. Neuron processing functions are thus influenced by changes in the biophysical properties of the synapse, such as long-term potentiation (LTP) or depression (LTD). This observation has opened new perspectives on the biophysical basis of learning and memory, but its quantitative impact on the information transmission of a neuron remains partially elucidated. One major obstacle is the high dimensionality of the neuronal input-output space, which makes it unfeasible to perform a thorough computational analysis of a neuron with multiple synaptic inputs. In this work, information theory was employed to characterize the information transmission of a cerebellar granule cell over a region of its excitatory input space following synaptic changes. Granule cells have a small dendritic tree (on average, they receive only four mossy fiber afferents), which greatly bounds the input combinatorial space, reducing the complexity of information-theoretic calculations. Numerical simulations and LTP experiments quantified how changes in neurotransmitter release probability (p) modulated information transmission of a cerebellar granule cell. Numerical simulations showed that p shaped the neurotransmission landscape in unexpected ways. As p increased, the optimality of the information transmission of most stimuli did not increase strictly monotonically; instead it reached a plateau at intermediate p levels. Furthermore, our results showed that the spatiotemporal characteristics of the inputs determine the effect of p on neurotransmission, thus permitting the selection of distinctive preferred stimuli for different p values. These selective mechanisms may have important consequences on the encoding of cerebellar mossy fiber inputs and the plasticity and computation at the next circuit stage, including the parallel fiber-Purkinje cell synapses.

We study an encoding/decoding mechanism accounting for the relative spike timing of the signals propagating from peripheral nerve fibers to second-order somatosensory neurons in the cuneate nucleus (CN). The CN is modeled as a population of spiking neurons receiving as inputs the spatiotemporal responses of real mechanoreceptors obtained via microneurography recordings in humans. The efficiency of the haptic discrimination process is quantified by a novel definition of entropy that takes into full account the metrical properties of the spike train space. This measure proves to be a suitable decoding scheme for generalizing the classical Shannon entropy to spike-based neural codes. It permits an assessment of neurotransmission in the presence of a large output space (i.e. hundreds of spike trains) with 1 ms temporal precision. It is shown that the CN population code performs a complete discrimination of 81 distinct stimuli already within 35 ms of the first afferent spike, whereas a partial discrimination (80% of the maximum information transmission) is possible as rapidly as 15 ms. This study suggests that the CN may not constitute a mere synaptic relay along the somatosensory pathway but, rather, it may convey optimal contextual accounts (in terms of fast and reliable information transfer) of peripheral tactile inputs to downstream structures of the central nervous system.

We study spatial learning and navigation for autonomous agents. A state space representation is constructed by unsupervised Hebbian learning during exploration. As a result of learning, a representation of the continuous two-dimensional (2-D) manifold in the high-dimensional input space is found. The representation consists of a population of localized overlapping place fields covering the 2-D space densely and uniformly. This space coding is comparable to the representation provided by hippocampal place cells in rats. Place fields are learned by extracting spatio-temporal properties of the environment from sensory inputs. The visual scene is modeled using the responses of modified Gabor filters placed at the nodes of a sparse Log-polar graph. Visual sensory aliasing is eliminated by taking into account self-motion signals via path integration. This solves the hidden state problem and provides a suitable representation for applying reinforcement learning in continuous space for action selection. A temporal-difference prediction scheme is used to learn sensorimotor mappings to perform goal-oriented navigation. Population vector coding is employed to interpret ensemble neural activity. The model is validated on a mobile Khepera miniature robot.

We model hippocampal place cells and head-direction cells by combin(cid:173) ing allothetic (visual) and idiothetic (proprioceptive) stimuli. Visual in(cid:173) put, provided by a video camera on a miniature robot, is preprocessed by a set of Gabor filters on 31 nodes of a log-polar retinotopic graph. Unsu(cid:173) pervised Hebbian learning is employed to incrementally build a popula(cid:173) tion of localized overlapping place fields. Place cells serve as basis func(cid:173) tions for reinforcement learning. Experimental results for goal-oriented navigation of a mobile robot are presented.

This paper presents an adaptive method that allows mobile robots to learn cognitive maps of indoor environments incrementally and online. Our approach models the environment. By means of a variable-resolution partitioning that discretizes the world in perceptually homogeneous regions. The resulting model incorporates both a compact geometrical representation of the environment and a topological map of the spatial relationships between its obstacle-free areas. The efficiency of the learning process is based on the use of local memory-based techniques for partitioning and of active learning techniques for selecting the most appropriate region to be explored next. In addition, a feedforward neural network is used to interpret sensor readings. We present experimental results obtained with two different mobile robots, the Nomad 200 and Khepera. The current implementation of the method relies on the assumption that obstacles are parallel or perpendicular to each other. This results in variable-resolution partitioning consisting of simple rectangular partitions and reduces the complexity of treating the underlying geometrical properties.