The clean waveforms are then used to infer the set of neural spike waveform templates through nonparametric Bayesian clustering.

We detail how, in our model, the calcium plateau potential can be interpreted as a backpropagating error signal.

Accurate modeling of neuronal action potential (AP) onset timing is crucial for understanding neural coding of danger signals. Traditional leaky integrate-and-fire (LIF) models, while widely used, exhibit high relative error in predicting AP onset latency, especially under strong or rapidly changing stimuli. Inspired by recent experimental findings and quantum theory, we present a quantum-inspired leaky integrate-and-fire (QI-LIF) model that treats AP onset as a probabilistic event, represented by a Gaussian wave packet in time. This approach captures the biological variability and uncertainty inherent in neuronal firing. We systematically compare the relative error of AP onset predictions between the classical LIF and QI-LIF models using synthetic data from hippocampal and sensory neurons subjected to varying stimulus amplitudes. Our results demonstrate that the QI-LIF model significantly reduces prediction error, particularly for high-intensity stimuli, aligning closely with observed biological responses. This work highlights the potential of quantum-inspired computational frameworks in advancing the accuracy of neural modeling and has implications for quantum engineering approaches to brain-inspired computing.

We detail how, in our model, the calcium plateau potential can be interpreted as a backpropagating error signal.

There is this risk if the corresponding parameter is chosen too small; but it did not seem to be a problem for the data used here.

Many neural circuits are composed of numerous distinct cell types that perform different operations on their inputs, and send their outputs to distinct targets. Therefore, a key step in understanding neural systems is to reliably distinguish cell types. An important example is the retina, for which present-day techniques for identifying cell types are accurate, but very labor-intensive. Here, we develop automated classifiers for functional identification of retinal ganglion cells, the output neurons of the retina, based solely on recorded voltage patterns on a large scale array. We use per-cell classifiers based on features extracted from electro-physiological images (spatiotemporal voltage waveforms) and interspike intervals (autocorrelations). These classifiers achieve high performance in distinguishing between the major ganglion cell classes of the primate retina, but fail in achieving the same accuracy in predicting cell polarities (ON vs. OFF). We then show how to use indicators of functional coupling within populations of ganglion cells (cross-correlation) to infer cell polarities with a matrix completion algorithm. This can result in accurate, fully automated methods for cell type classification.

Technological advances in the past decades have begun to enable neuroscientists to address fundamental questions about consciousness in an unprecedented way. Here we review remarkable recent progress in our understanding of cellular-level mechanisms of conscious processing in the brain. Of particular interest are the cortical pyramidal neurons -- or "psychic cells" called by Ramón y Cajal more than 100 years ago -- which have an intriguing cellular mechanism that accounts for selective disruption of feedback signaling in the brain upon anesthetic-induced loss of consciousness. Importantly, a particular class of metabotropic receptors distributed over the dendrites of pyramidal cells are highlighted as the key cellular mechanism. After all, Cajal's instinct over a century ago may turn out to be correct -- we may have just begun to understand whether and how psychic cells indeed generate and control our consciousness.

The past few years have seen a surge in the application of quantum theory methodologies and quantum-like modeling in fields such as cognition, psychology, and decision-making. Despite the success of this approach in explaining various psychological phenomena such as order, conjunction, disjunction, and response replicability effects there remains a potential dissatisfaction due to its lack of clear connection to neurophysiological processes in the brain. Currently, it remains a phenomenological approach. In this paper, we develop a quantum-like representation of networks of communicating neurons. This representation is not based on standard quantum theory but on generalized probability theory (GPT), with a focus on the operational measurement framework. Specifically, we use a version of GPT that relies on ordered linear state spaces rather than the traditional complex Hilbert spaces. A network of communicating neurons is modeled as a weighted directed graph, which is encoded by its weight matrix. The state space of these weight matrices is embedded within the GPT framework, incorporating effect observables and state updates within the theory of measurement instruments a critical aspect of this model. This GPT based approach successfully reproduces key quantum-like effects, such as order, non-repeatability, and disjunction effects (commonly associated with decision interference). Moreover, this framework supports quantum-like modeling in medical diagnostics for neurological conditions such as depression and epilepsy. While this paper focuses primarily on cognition and neuronal networks, the proposed formalism and methodology can be directly applied to a wide range of biological and social networks.

Neural Information Processing Systems http://nips.cc/

Mathematical modeling in systems toxicology enables a comprehensive understanding of the effects of pharmaceutical substances on cardiac health. However, the complexity of these models limits their widespread application in early drug discovery. In this paper, we introduce a novel approach to solving parameterized models of cardiac action potentials by combining meta-learning techniques with Systems Biology-Informed Neural Networks (SBINNs). The proposed method, HyperSBINN, effectively addresses the challenge of predicting the effects of various compounds at different concentrations on cardiac action potentials, outperforming traditional differential equation solvers in speed. Our model efficiently handles scenarios with limited data and complex parameterized differential equations. The HyperSBINN model demonstrates robust performance in predicting APD90 values, indicating its potential as a reliable tool for modeling cardiac electrophysiology and aiding in preclinical drug development. This framework represents an advancement in computational modeling, offering a scalable and efficient solution for simulating and understanding complex biological systems.