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1.
J Neural Eng ; 10(4): 046019, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23883543

RESUMO

OBJECTIVE: Fine touch sensing relies on peripheral-to-central neurotransmission of somesthetic percepts, as well as on active motion policies shaping tactile exploration. This paper presents a novel neuroengineering framework for robotic applications based on the multistage processing of fine tactile information in the closed action-perception loop. APPROACH: The integrated system modules focus on (i) neural coding principles of spatiotemporal spiking patterns at the periphery of the somatosensory pathway, (ii) probabilistic decoding mechanisms mediating cortical-like tactile recognition and (iii) decision-making and low-level motor adaptation underlying active touch sensing. We probed the resulting neural architecture through a Braille reading task. MAIN RESULTS: Our results on the peripheral encoding of primary contact features are consistent with experimental data on human slow-adapting type I mechanoreceptors. They also suggest second-order processing by cuneate neurons may resolve perceptual ambiguities, contributing to a fast and highly performing online discrimination of Braille inputs by a downstream probabilistic decoder. The implemented multilevel adaptive control provides robustness to motion inaccuracy, while making the number of finger accelerations covariate with Braille character complexity. The resulting modulation of fingertip kinematics is coherent with that observed in human Braille readers. SIGNIFICANCE: This work provides a basis for the design and implementation of modular neuromimetic systems for fine touch discrimination in robotics.


Assuntos
Biorretroalimentação Psicológica/instrumentação , Biorretroalimentação Psicológica/fisiologia , Biomimética/instrumentação , Mecanorreceptores/fisiologia , Mecanotransdução Celular/fisiologia , Robótica/instrumentação , Tato/fisiologia , Simulação por Computador , Desenho de Equipamento , Análise de Falha de Equipamento , Retroalimentação Fisiológica/fisiologia , Humanos , Modelos Biológicos , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Processamento de Sinais Assistido por Computador/instrumentação
2.
Neuroscience ; 165(3): 692-704, 2010 Feb 03.
Artigo em Inglês | MEDLINE | ID: mdl-19922773

RESUMO

The intact brain is continuously targeted by a wealth of stimuli with distinct spatio-temporal patterns which modify, since the very beginning of development, the activity and the connectivity of neuronal networks. In this paper, we used dissociated neuronal cultures coupled to microelectrode arrays (MEAs) to study the response of cortical neuron assemblies to low-frequency stimuli constantly delivered over weeks in vitro. We monitored the spontaneous activity of the cultures before and after the stimulation sessions, as well as their evoked response to the stimulus. During in vitro development, the vast majority of the cultures responded to the stimulation by significantly increasing the bursting activity and a widespread stabilization of electrical activity was observed after the third week of age. A similar trend was present between the spontaneous activity of the networks observed over 30 min after the stimulus and the responses evoked by the stimulus itself, although no significant differences in spontaneous activity were detected between stimulated and non-stimulated cultures belonging to the same preparations. The data indicate that the stimulation had a delayed effect modulating responsiveness capability of the network without directly affecting its intrinsic in vitro development.


Assuntos
Córtex Cerebral/fisiologia , Neurônios/fisiologia , Potenciais de Ação , Animais , Técnicas de Cultura de Células , Células Cultivadas , Estimulação Elétrica , Microeletrodos , Ratos , Ratos Sprague-Dawley , Fatores de Tempo
3.
Neuroscience ; 153(4): 1354-69, 2008 Jun 02.
Artigo em Inglês | MEDLINE | ID: mdl-18448256

RESUMO

Dissociated cortical neurons from rat embryos cultured onto micro-electrode arrays exhibit characteristic patterns of electrophysiological activity, ranging from isolated spikes in the first days of development to highly synchronized bursts after 3-4 weeks in vitro. In this work we analyzed these features by considering the approach proposed by the self-organized criticality theory: we found that networks of dissociated cortical neurons also generate spontaneous events of spreading activity, previously observed in cortical slices, in the form of neuronal avalanches. Choosing an appropriate time scale of observation to detect such neuronal avalanches, we studied the dynamics by considering the spontaneous activity during acute recordings in mature cultures and following the development of the network. We observed different behaviors, i.e. sub-critical, critical or super-critical distributions of avalanche sizes and durations, depending on both the age and the development of cultures. In order to clarify this variability, neuronal avalanches were correlated with other statistical parameters describing the global activity of the network. Criticality was found in correspondence to medium synchronization among bursts and high ratio between bursting and spiking activity. Then, the action of specific drugs affecting global bursting dynamics (i.e. acetylcholine and bicuculline) was investigated to confirm the correlation between criticality and regulated balance between synchronization and variability in the bursting activity. Finally, a computational model of neuronal network was developed in order to interpret the experimental results and understand which parameters (e.g. connectivity, excitability) influence the distribution of avalanches. In summary, cortical neurons preserve their capability to self-organize in an effective network even when dissociated and cultured in vitro. The distribution of avalanche features seems to be critical in those cultures displaying medium synchronization among bursts and poor random spiking activity, as confirmed by chemical manipulation experiments and modeling studies.


Assuntos
Córtex Cerebral/citologia , Rede Nervosa/fisiologia , Neurônios/fisiologia , Acetilcolina/farmacologia , Potenciais de Ação/efeitos dos fármacos , Potenciais de Ação/fisiologia , Animais , Células Cultivadas , Embrião de Mamíferos , Modelos Neurológicos , Rede Nervosa/efeitos dos fármacos , Neurônios/efeitos dos fármacos , Ratos , Fatores de Tempo
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