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Register a new userElectrocorticogram encoding of upper extremity movement trajectories
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Electrocorticogram (ECoG)-based brain computer interfaces (BCI) can potentially control upper extremity prostheses to restore independent function to paralyzed individuals. However, current research is mostly restricted to the offline decoding of finger or 2D arm movement trajectories, and these results are modest. This study seeks to improve the fundamental understanding of the ECoG signal features underlying upper extremity movements to guide better BCI design. Subjects undergoing ECoG electrode implantation performed a series of elementary upper extremity movements in an intermittent flexion and extension manner. It was found that movement velocity, $dottheta$, had a high positive (negative) correlation with the instantaneous power of the ECoG high-$gamma$ band (80-160 Hz) during flexion (extension). Also, the correlation was low during idling epochs. Visual inspection of the ECoG high-$gamma$ band revealed power bursts during flexion/extension events that have a waveform that strongly resembles the corresponding flexion/extension event as seen on $dottheta$. These high-$gamma$ bursts were present in all elementary movements, and were spatially distributed in a somatotopic fashion. Thus, it can be concluded that the high-$gamma$ power of ECoG strongly encodes for movement trajectories, and can be used as an input feature in future BCIs.
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Brain-computer interfaces (BCIs) have shown promising results in restoring motor function to individuals with spinal cord injury. These systems have traditionally focused on the restoration of upper extremity function; however, the lower extremities have received relatively little attention. Early feasibility studies used noninvasive electroencephalogram (EEG)-based BCIs to restore walking function to people with paraplegia. However, the limited spatiotemporal resolution of EEG signals restricted the application of these BCIs to elementary gait tasks, such as the initiation and termination of walking. To restore more complex gait functions, BCIs must accurately decode additional degrees of freedom from brain signals. In this study, we used subdurally recorded electrocorticogram (ECoG) signals from able-bodied subjects to design a decoder capable of predicting the walking state and step rate information. We recorded ECoG signals from the motor cortices of two individuals as they walked on a treadmill at different speeds. Our offline analysis demonstrated that the state information could be decoded from >16 minutes of ECoG data with an unprecedented accuracy of 99.8%. Additionally, using a Bayesian filter approach, we achieved an average correlation coefficient between the decoded and true step rates of 0.934. When combined, these decoders may yield decoding accuracies sufficient to safely operate present-day walking prostheses.
Many cells use calcium signalling to carry information from the extracellular side of the plasma membrane to targets in their interior. Since virtually all cells employ a network of biochemical reactions for Ca2+ signalling, much effort has been devoted to understand the functional role of Ca2+ responses and to decipher how their complex dynamics is regulated by the biochemical network of Ca2+-related signal transduction pathways. Experimental observations show that Ca2+ signals in response to external stimuli encode information via frequency modulation or alternatively via amplitude modulation. Although minimal models can capture separately both types of dynamics, they fail to exhibit different and more advanced encoding modes. By arguments of bifurcation theory, we propose instead that under some biophysical conditions more complex modes of information encoding can also be manifested by minimal models. We consider the minimal model of Li and Rinzel and show that information encoding can occur by amplitude modulation (AM) of Ca2+ oscillations, by frequency modulation (FM) or by both modes (AFM). Our work is motivated by calcium signalling in astrocytes, the predominant type of cortical glial cells that is nowadays recognized to play a crucial role in the regulation of neuronal activity and information processing of the brain. We explain that our results can be crucial for a better understanding of synaptic information transfer. Furthermore, our results might also be important for better insight on other examples of physiological processes regulated by Ca2+ signalling.
Neural coding is a field of study that concerns how sensory information is represented in the brain by networks of neurons. The link between external stimulus and neural response can be studied from two parallel points of view. The first, neural encoding refers to the mapping from stimulus to response, and primarily focuses on understanding how neurons respond to a wide variety of stimuli, and on constructing models that accurately describe the stimulus-response relationship. Neural decoding, on the other hand, refers to the reverse mapping, from response to stimulus, where the challenge is to reconstruct a stimulus from the spikes it evokes. Since neuronal response is stochastic, a one-to-one mapping of stimuli into neural responses does not exist, causing a mismatch between the two viewpoints of neural coding. Here, we use these two perspectives to investigate the question of what rate coding is, in the simple setting of a single stationary stimulus parameter and a single stationary spike train represented by a renewal process. We show that when rate codes are defined in terms of encoding, i.e., the stimulus parameter is mapped onto the mean firing rate, the rate decoder given by spike counts or the sample mean, does not always efficiently decode the rate codes, but can improve efficiency in reading certain rate codes, when correlations within a spike train are taken into account.
Participants in an eye-movement experiment performed a modified version of the Landolt-C paradigm (Williams & Pollatsek, 2007) in which they searched for target squares embedded in linear arrays of spatially contiguous words (i.e., short sequences of squares having missing segments of variable size and orientation). Although the distributions of single- and first-of-multiple fixation locations replicated previous patterns suggesting saccade targeting (e.g., Yan, Kliegl, Richter, Nuthmann, & Shu, 2010), the distribution of all forward fixation locations was uniform, suggesting the absence of specific saccade targets. Furthermore, properties of the words (e.g., gap size) also influenced fixation durations and forward saccade length, suggesting that on-going processing affects decisions about when and where (i.e., how far) to move the eyes. The theoretical implications of these results for existing and future accounts of eye-movement control are discussed.
A good understanding of how neurons use electrical pulses (i.e, spikes) to encode the signal information remains elusive. Analyzing spike sequences generated by individual neurons and by two coupled neurons (using the stochastic FitzHugh-Nagumo model), recent theoretical studies have found that the relative timing of the spikes can encode the signal information. Using a symbolic method to analyze the spike sequence, preferred and infrequent spike patterns were detected, whose probabilities vary with both, the amplitude and the frequency of the signal. To investigate if this encoding mechanism is plausible also for neuronal ensembles, here we analyze the activity of a group of neurons, when they all perceive a weak periodic signal. We find that, as in the case of one or two coupled neurons, the probabilities of the spike patterns, now computed from the spike sequences of all the neurons, depend on the signals amplitude and period, and thus, the patterns probabilities encode the information of the signal. We also find that the resonances with the period of the signal or with the noise level are more pronounced when a group of neurons perceive the signal, in comparison with when only one or two coupled neurons perceive it. Neuronal coupling is beneficial for signal encoding as a group of neurons is able to encode a small-amplitude signal, which could not be encoded when it is perceived by just one or two coupled neurons. Interestingly, we find that for a group of neurons, just a few connections with one another can significantly improve the encoding of small-amplitude signals. Our findings indicate that information encoding in preferred and infrequent spike patterns is a plausible mechanism that can be employed by neuronal populations to encode weak periodic inputs, exploiting the presence of neural noise.
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