Network anomaly detection systems encounter several challenges with traditional detectors trained offline. They become susceptible to concept drift and new threats such as zero-day or polymorphic attacks. To address this limitation, we propose a Ca$^{2+}$-modulated learning framework that draws inspiration from astrocytic Ca$^{2+}$ signaling in the brain, where rapid, context-sensitive adaptation enables robust information processing. Our approach couples a multicellular astrocyte dynamics simulator with a deep neural network (DNN). The simulator models astrocytic Ca$^{2+}$ dynamics through three key mechanisms: IP$_3$-mediated Ca$^{2+}$ release, SERCA pump uptake, and conductance-aware diffusion through gap junctions between cells. Evaluation of our proposed network on CTU-13 (Neris) network traffic data demonstrates the effectiveness of our biologically plausible approach. The Ca$^{2+}$-gated model outperforms a matched baseline DNN, achieving up to $\sim$98\% accuracy with reduced false positives and negatives across multiple train/test splits. Importantly, this improved performance comes with negligible runtime overhead once Ca$^{2+}$ trajectories are precomputed. While demonstrated here for cybersecurity applications, this Ca$^{2+}$-modulated learning framework offers a generic solution for streaming detection tasks that require rapid, biologically grounded adaptation to evolving data patterns.

Autonomy is a hallmark of animal intelligence, enabling adaptive and intelligent behavior in complex environments without relying on external reward or task structure. Existing reinforcement learning approaches to exploration in reward-free environments, including a class of methods known as model-based intrinsic motivation, exhibit inconsistent exploration patterns and do not converge to an exploratory policy, thus failing to capture robust autonomous behaviors observed in animals. Moreover, systems neuroscience has largely overlooked the neural basis of autonomy, focusing instead on experimental paradigms where animals are motivated by external reward rather than engaging in ethological, naturalistic and task-independent behavior. To bridge these gaps, we introduce a novel model-based intrinsic drive explicitly designed after the principles of autonomous exploration in animals. Our method (3M-Progress) achieves animal-like exploration by tracking divergence between an online world model and a fixed prior learned from an ecological niche. To the best of our knowledge, we introduce the first autonomous embodied agent that predicts brain data entirely from self-supervised optimization of an intrinsic goal -- without any behavioral or neural training data -- demonstrating that 3M-Progress agents capture the explainable variance in behavioral patterns and whole-brain neural-glial dynamics recorded from autonomously behaving larval zebrafish, thereby providing the first goal-driven, population-level model of neural-glial computation. Our findings establish a computational framework connecting model-based intrinsic motivation to naturalistic behavior, providing a foundation for building artificial agents with animal-like autonomy.

Astrocytes are critical glial cells whose altered morphology and density are hallmarks of many neurological disorders. However, their intricate branching and stain dependent variability make automated detection of histological images a highly challenging task. To address these challenges, we propose a hybrid CNN Transformer detector that combines local feature extraction with global contextual reasoning. A heatmap guided query mechanism generates spatially grounded anchors for small and faint astrocytes, while a lightweight Transformer module improves discrimination in dense clusters. Evaluated on ALDH1L1 and GFAP stained astrocyte datasets, the model consistently outperformed Faster R-CNN, YOLOv11 and DETR, achieving higher sensitivity with fewer false positives, as confirmed by FROC analysis. These results highlight the potential of hybrid CNN Transformer architectures for robust astrocyte detection and provide a foundation for advanced computational pathology tools.

The process is formalized below.

--Preliminary attempts at incorporating the critical role of astrocytes--cells that constitute more than 50% of human brain cells--in brain-inspired neuromorphic computing remain in infancy. This paper seeks to delve deeper into various key aspects of neuron-synapse-astrocyte interactions to mimic self-attention mechanisms in Transformers. The cross-layer perspective explored in this work involves bioplausible modeling of Hebbian and presynaptic plasticities in neuron-astrocyte networks, incorporating effects of non-linearities and feedback along with algorithmic formulations to map the neuron-astrocyte computations to self-attention mechanism and evaluating the impact of incorporating bio-realistic effects from the machine learning application side. Our analysis on sentiment and image classification tasks (IMDB and CIF AR10 datasets) highlights the advantages of Astromorphic Transformers, offering improved accuracy and learning speed. Furthermore, the model demonstrates strong natural language generation capabilities on the WikiT ext-2 dataset, achieving better perplexity compared to conventional models, thus showcasing enhanced generalization and stability across diverse machine learning tasks. STROCYTES, a type of glial cell, play a critical role in brain function, encompassing various processes such as homeostasis, metabolism, and synaptic regulation [1]. Astrocytes detect and regulate synaptic activity in the tripartite synapse through interactions with pre-and postsynaptic neurons. Investigating their impact on neural computation is currently an active research field in neuroscience and underscores the critical need to move beyond the neuro-synaptic perspective of current Artificial Intelligence (AI) systems. Recent experimental findings on neuron-astrocyte interactions and modulation have led to significant progress in computational neuroscience, enabling the development of models that incorporate neuron-astrocyte interactions within neural networks [2], [3]. Astrocytes have been found to modulate bursting in neural circuitry through the release of gliotransmitters, which have an impact on neuronal excitability and synaptic plasticity [4], [5]. Astrocytes possess the ability to encode information through calcium signaling and regulate information processing, thereby actively engaging in neural computation at the tripartite synapse level. Additionally, astrocytes possess inherent capacity as memory components [6], [7] and plasticity regulators that are capable of facilitating local sequential learning [8], [9].

Biological systems are non-linear, include unobserved variables and the physical principles that govern their dynamics are partly unknown. This makes the characterization of their behavior very challenging. Notably, their activity occurs on multiple interdependent spatial and temporal scales that require linking mechanisms across scales. To address the challenge of bridging gaps between scales, we leverage partial differential equations (PDE) discovery. PDE discovery suggests meso-scale dynamics characteristics from micro-scale data. In this article, we present our framework combining particle-based simulations and PDE discovery and conduct preliminary experiments to assess equation discovery in controlled settings. We evaluate five state-of-the-art PDE discovery methods on particle-based simulations of calcium diffusion in astrocytes. The performances of the methods are evaluated on both the form of the discovered equation and the forecasted temporal variations of calcium concentration. Our results show that several methods accurately recover the diffusion term, highlighting the potential of PDE discovery for capturing macroscopic dynamics in biological systems from microscopic data.

Machine learning models achieve high precision, but their decision-making processes often lack explainability. Furthermore, as model complexity increases, explainabil-ity typically decreases. Existing efforts to improve explain-ability primarily involve developing new eXplainable artificial intelligence (XAI) techniques or incorporating explain-ability constraints during training. While these approaches yield specific improvements, their applicability remains limited. In this work, we propose the Vision Transformer with artificial Astrocytes (ViTA). This training-free approach is inspired by neuroscience and enhances the reasoning of a pretrained deep neural network to generate more human-aligned explanations. W e evaluated our approach employing two well-known XAI techniques, Grad-CAM and Grad-CAM++, and compared it to a standard Vision Transformer (ViT). Using the ClickMe dataset, we quantified the similarity between the heatmaps produced by the XAI techniques and a (human-aligned) ground truth. Our results consistently demonstrate that incorporating artificial astrocytes enhances the alignment of model explanations with human perception, leading to statistically significant improvements across all XAI techniques and metrics utilized.

Traditional artificial neural networks take inspiration from biological networks, using layers of neuron-like nodes to pass information for processing. More realistic models include spiking in the neural network, capturing the electrical characteristics more closely. However, a large proportion of brain cells are of the glial cell type, in particular astrocytes which have been suggested to play a role in performing computations. Here, we introduce a modified spiking neural network model with added astrocyte-like units in a neural network and asses their impact on learning. We implement the network as a liquid state machine and task the network with performing a chaotic time-series prediction task. We varied the number and ratio of neuron-like and astrocyte-like units in the network to examine the latter units effect on learning. We show that the combination of neurons and astrocytes together, as opposed to neural- and astrocyte-only networks, are critical for driving learning. Interestingly, we found that the highest learning rate was achieved when the ratio between astrocyte-like and neuron-like units was roughly 2 to 1, mirroring some estimates of the ratio of biological astrocytes to neurons. Our results demonstrate that incorporating astrocyte-like units which represent information across longer timescales can alter the learning rates of neural networks, and the proportion of astrocytes to neurons should be tuned appropriately to a given task.

Within the complex neuroarchitecture of the brain, astrocytes play crucial roles in development, structure, and metabolism. These cells regulate neural activity through tripartite synapses, directly impacting cognitive processes such as learning and memory. Despite the growing recognition of astrocytes' significance, traditional Spiking Neural Network (SNN) models remain predominantly neuron-centric, overlooking the profound influence of astrocytes on neural dynamics. Inspired by these biological insights, we have developed an Astrocyte-Modulated Spiking Unit (AM-SU), an innovative framework that integrates neuron-astrocyte interactions into the computational paradigm, demonstrating wide applicability across various hardware platforms. Our Astrocyte-Modulated Spiking Neural Network (AstroSNN) exhibits exceptional performance in tasks involving memory retention and natural language generation, particularly in handling long-term dependencies and complex linguistic structures. The design of AstroSNN not only enhances its biological authenticity but also introduces novel computational dynamics, enabling more effective processing of complex temporal dependencies. Furthermore, AstroSNN shows low latency, high throughput, and reduced memory usage in practical applications, making it highly suitable for resource-constrained environments. By successfully integrating astrocytic dynamics into intelligent neural networks, our work narrows the gap between biological plausibility and neural modeling, laying the groundwork for future biologically-inspired neural computing research that includes both neurons and astrocytes.