Protocol for dissecting cascade computational components in neural networks of a visual system

Finding the complete functional circuits of neurons is a challenging problem in brain research. Here, we present a protocol, based on visual stimuli and spikes, for obtaining the complete circuit of recorded neurons using spike-triggered nonnegative matrix factorization. We describe steps for data preprocessing, inferring the spatial receptive field of the subunits, and analyzing the module matrix. This approach identifies computational components of the feedforward network of retinal ganglion cells and dissects the network structure based on natural image stimuli.For complete details on the use and execution of this protocol, please refer to Jia et al. (2021).

Spike timing reshapes robustness against attacks in spiking neural networks

The success of deep learning in the past decade is partially shrouded in the shadow of adversarial attacks. In contrast, the brain is far more robust at complex cognitive tasks. Utilizing the advantage that neurons in the brain communicate via spikes, spiking neural networks (SNNs) are emerging as a new type of neural network model, boosting the frontier of theoretical investigation and empirical application of artificial neural networks and deep learning. Neuroscience research proposes that the precise timing of neural spikes plays an important role in the information coding and sensory processing of the biological brain. However, the role of spike timing in SNNs is less considered and far from understood. Here we systematically explored the timing mechanism of spike coding in SNNs, focusing on the robustness of the system against various types of attacks. We found that SNNs can achieve higher robustness improvement using the coding principle of precise spike timing in neural encoding and decoding, facilitated by different learning rules. Our results suggest that the utility of spike timing coding in SNNs could improve the robustness against attacks, providing a new approach to reliable coding principles for developing next-generation brain-inspired deep learning

Neural System Identification with Spike-triggered Non-negative Matrix Factorization

Neuronal circuits formed in the brain are complex with intricate connection patterns. Such complexity is also observed in the retina as a relatively simple neuronal circuit. A retinal ganglion cell receives excitatory inputs from neurons in previous layers as driving forces to fire spikes. Analytical methods are required that can decipher these components in a systematic manner. Recently a method termed spike-triggered non-negative matrix factorization (STNMF) has been proposed for this purpose. In this study, we extend the scope of the STNMF method. By using the retinal ganglion cell as a model system, we show that STNMF can detect various computational properties of upstream bipolar cells, including spatial receptive field, temporal filter, and transfer nonlinearity. In addition, we recover synaptic connection strengths from the weight matrix of STNMF. Furthermore, we show that STNMF can separate spikes of a ganglion cell into a few subsets of spikes where each subset is contributed by one presynaptic bipolar cell. Taken together, these results corroborate that STNMF is a useful method for deciphering the structure of neuronal circuits.Comment: updated versio

Modelling the permeability of random discontinuous carbon fibre preforms

A force-directed algorithm was developed to create representative geometrical models of fibre distributions in directed carbon fibre preforms. Local permeability values were calculated for the preform models depending on the local fibre orientation, distribution and volume fraction. The effect of binder content was incorporated by adjusting the principal permeability values of the meso-scale discontinuous fibre bundles, using corresponding experimental data obtained for unidirectional non-crimp fabrics. The model provides an upper boundary for the permeability of directed carbon fibre preform architectures, where predictions are within one standard deviation of the experimental mean for all architectures studied

Robust Decoding of Rich Dynamical Visual Scenes With Retinal Spikes

Sensory information transmitted to the brain activates neurons to create a series of coping behaviors. Understanding the mechanisms of neural computation and reverse engineering the brain to build intelligent machines requires establishing a robust relationship between stimuli and neural responses. Neural decoding aims to reconstruct the original stimuli that trigger neural responses. With the recent upsurge of artificial intelligence, neural decoding provides an insightful perspective for designing novel algorithms of brain-machine interface. For humans, vision is the dominant contributor to the interaction between the external environment and the brain. In this study, utilizing the retinal neural spike data collected over multi trials with visual stimuli of two movies with different levels of scene complexity, we used a neural network decoder to quantify the decoded visual stimuli with six different metrics for image quality assessment establishing comprehensive inspection of decoding. With the detailed and systematical study of the effect and single and multiple trials of data, different noise in spikes, and blurred images, our results provide an in-depth investigation of decoding dynamical visual scenes using retinal spikes. These results provide insights into the neural coding of visual scenes and services as a guideline for designing next-generation decoding algorithms of neuroprosthesis and other devices of brain-machine interface.</p

Potential biomarkers of Parkinson’s disease revealed by plasma metabolic profiling

The plasma of Parkinson's disease (PD) patients may contain various altered metabolites associated with the risk or progression of the disease. Characterization of the abnormal metabolic pattern in PD plasma is therefore critical for the search for potential PD biomarkers. We collected blood plasma samples from PD patients and used an LC-MS based metabolomics approach to identify 17 metabolites with significantly altered levels. Metabolic network analysis was performed to place the metabolites linked to different pathways. The metabolic pathways involved were associated with tyrosine biosynthesis, glycerol phospholipid metabolism, carnitine metabolism and bile acid biosynthesis, within which carnitine and bile acid metabolites as potential biomarkers are first time reported. These abnormal metabolic changes in the plasma of patients with PD were mainly related to lipid metabolism and mitochondrial function