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McDougal, R. A.

Publications and source records attributed to McDougal, R. A..

11 recordsLinked to original sources

All Models are Wrong, Some are Annotated: Automating Metadata in Biomedical Repositories

ObjectiveHigh-quality metadata is essential for scientific discovery, yet sparse annotations in rapidly growing repositories leave many biologically relevant details uncaptured. We evaluated whether large language models (LLMs) can accurately infer ion channel and receptor subtype metadata from source code in a neuroscience repository. Materials and MethodsWe extracted 5,133 model files from ModelDB. A subset of 1,100 was manually annotated; 253 were held out for testing, and the remainder split into training (80%) and validation (20%) sets. LLM-based approaches (GPT-5.2 and GPT-mini) were evaluated under zero-shot and heuristic-augmented prompting. Performance was assessed at type and subtype levels using accuracy, precision, recall, and F1 score. A feature-engineered XGBoost model using text- and simulation-derived features served as a baseline. ResultsLLMs outperformed the XGBoost baseline. At the type level, GPT-mini with heuristic augmentation achieved the highest performance (accuracy 96.0%, F1 0.962). At the subtype level, both GPT-5.2+heuristics and GPT-mini+heuristics achieved identical accuracy (88.1%), with GPT-5.2+heuristics achieving the highest F1(0.878). Model outputs were consistent across runs and errors confined to related mechanistic families. Discussion and ConclusionLLMs demonstrate strong potential for metadata annotation directly from source code, outperforming feature-engineering approaches with minimal tuning. However, performance varied across subtypes, and errors often reflected ambiguity or bias toward more common labels. These findings suggest LLMs may serve as practical tools for scalable metadata generation in biomedical repositories, although careful evaluation and domain-specific validation remain important. While demonstrated in computational neuroscience, this approach may generalize to repository-agnostic metadata annotation in other scientific code repositories.

neuroscience↗

Local homeostatic scaling supports stable rate propagation under noise and heterogeneity

Reliable transmission of firing-rate signals through neural circuits requires synaptic coupling to remain within a narrow regime shaped by neuronal heterogeneity and noise. Outside this regime, classical theory predicts that activity will dissipate or amplify into synchrony. Studies have shown that stable rate-code transmission is biologically achievable, but they leave open how the required operating regime is established. Canonical plasticity rules including Hebbian plasticity and conventional homeostatic scaling do not by themselves recover this regime. We therefore introduce relational homeostatic scaling, a local synaptic scaling rule in which each postsynaptic neuron adjusts its total excitatory afferent strength to reduce the discrepancy between a recent AMPA-weighted afferent activity trace and a recent postsynaptic activity trace. Together, these traces capture the recent rate entering and leaving the neuron without requiring a global rate target. Mean-field analysis and simulations show that this rule drives synaptic weights toward the critical regime without precise weight initialization. The rule remains robust to neuronal heterogeneity, composes with spike-timing-dependent plasticity without disrupting Hebbian competition, and stabilizes the eligibility trace required by three-factor learning rules. These findings suggest that relational homeostatic scaling may provide a substrate for stable rate-code transmission in neural circuits. Author SummaryNeural signals often pass through many processing stages, but this is difficult in networks made of noisy and heterogeneous neurons. Classical feedforward models predict that activity will either fade away or become too synchronized unless synaptic strengths fall within a narrow stable regime. Recent studies have shown that biological neural networks can transmit firing-rate information reliably. How do neural circuits find and maintain the operating regime needed for stable rate-code transmission? We propose a simple local mechanism, relational homeostatic scaling, in which each neuron adjusts the strength of its incoming excitatory synapses by comparing a recent trace of its input activity with a trace of its own activity. Unlike conventional homeostatic scaling, the goal is not to force every neuron toward a fixed firing rate. The goal is to preserve the relationship between input drive and output activity. We show that this rule allows layered spiking networks to self-organize into the stable transmission regime, remains robust to neuronal heterogeneity, and works alongside Hebbian spike-timing plasticity. These results suggest that homeostatic plasticity may help establish the circuit conditions under which experimentally observed rate-code transmission can occur.

neuroscience↗

Computer models predict differential dendritic vulnerability with ischemia and spreading depression

Ischemia, whether abrupt or chronic, limits ATP production and disrupts ATP-dependent homeostatic mechanisms, leading to alterations in both intracellular and extracellular ion concentrations. Inadequate neuronal ATP triggers K+ release and increased extracellular K+ depolarizes neurons, leading to additional K+ release; this positive feedback phenomenon is known as spreading depolarization (SD). When the depolarizing effects are strong enough, the cells undergo depolarization blockade, known as spreading depression. Excess extracellular K+ increases energy demand from the Na+-K+ pump, producing a pathological confluence of increased demand with reduced delivery of energy. The resulting changes have profound effects at subcellular, cellular, and network scales of brain function. We hypothesized that consequences of ischemic or SD homeostatic failure would differ on the subcellular scale, with differences between disjunct dendritic regions of a hippocampal CA1 pyramidal neuron. To evaluate the interplay between morphology and ion concentrations, we used a mechanistic simulation incorporating neuronal morphology, pumps, exchangers, voltage-, and Ca2+-sensitive ion channels. In both cases, calcium accumulation was greatest in the basilar dendrites, suggesting these dendrites would show the greatest effects of excitotoxicity. By contrast, ischemia, but not SD showed that distal apical dendrites were exposed to greater intracellular chloride concentrations, which may lead to dendritic beading.

neuroscience↗

Automating literature screening and curation with applications to computational neuroscience

ObjectiveModelDB (https://modeldb.science) is a discovery platform for computational neuroscience, containing over 1800 published model codes with standardized metadata. These codes were mainly supplied from unsolicited model author submissions, but this approach is inherently limited. We estimate we have captured only around one-third of NEURON models and lower fractions for other simulators. To more completely characterize the state of computational neuroscience modeling work, we aim to identify works containing results derived from computational neuroscience approaches and their standardized associated metadata (e.g. cell types, research topics). Materials and MethodsKnown computational neuroscience work from ModelDB and identified neuroscience work queried from PubMed were included in our study. After pre-screening with SPECTER2, GPT-3.5 and GPT-4 were used to identify likely computational neuroscience work and their relevant metadata. ResultsSPECTER2, GPT-4, and GPT-3.5 demonstrated varied but high abilities in identification of computational neuroscience work. GPT-4 achieved 96.9% accuracy and GPT-3.5 improved from 54.2% to 85.5% through instruction-tuning and Chain of Thought. GPT-4 also showed high potential in identifying relevant metadata annotations. DiscussionDue to computational limitations, we only used each papers title and abstract, partially leading to false negatives. Further efforts should be devoted to including more training data and further improving current LLMs through fine-tuning approaches. ConclusionNLP and LLM techniques can be added to ModelDB to facilitate further model discovery, and will contribute to a more standardized and comprehensive framework for establishing domain-specific resources.

neuroscience↗

Reproducibility of biophysical in silico neuron states and spikes from event-based partial histories

Biophysically detailed simulations attempting to reproduce neuronal activity often rely on solving large systems of differential equations; in some models, these systems have tens of thousands of states per cell. Numerically solving these equations is computationally intensive and requires making assumptions about the initial cell states. Additional realism from incorporating more biological detail is achieved at the cost of increasingly more states, more computational resources, and more modeling assumptions. We show that for both point and morphologically-detailed cell models, the presence and timing of future action potentials is probabilistically well-characterized by the relative timings of a small number of recent synaptic events alone. Knowledge of initial conditions or full synaptic input history is not a requirement. While model time constants, etc. impact the specifics, we demonstrate that for both individual spikes and sustained cellular activity, the uncertainty in spike response decreases to the point of approximate determinism. Further, we show cellular model states are reconstructable from ongoing synaptic events, despite unknown initial conditions. We propose that a strictly event-based modeling framework is capable of representing the full complexity of cellular dynamics of the differential-equations models with significantly less per-cell state variables, thus offering a pathway toward utilizing modern data-driven modeling to scale up to larger network models while preserving individual cellular biophysics.

neuroscience↗

Modernizing the NEURON Simulator for Sustainability, Portability, and Performance

AO_SCPLOWBSTRACTC_SCPLOWThe need for reproducible, credible, multiscale biological modeling has led to the development of standardized simulation platforms, such as the widely-used NEURON environment for computational neuroscience. Developing and maintaining NEURON over several decades has required attention to the competing needs of backwards compatibility, evolving computer architectures, the addition of new scales and physical processes, accessibility to new users, and efficiency and flexibility for specialists. In order to meet these challenges, we have now substantially modernized NEURON, providing continuous integration, an improved build system and release workflow, and better documentation. With the help of a new source-to-source compiler of the NMODL domain-specific language we have enhanced NEURONs ability to run efficiently, via the CoreNEURON simulation engine, on a variety of hardware platforms, including GPUs. Through the implementation of an optimized in-memory transfer mechanism this performance optimized backend is made easily accessible to users, providing training and model-development paths from laptop to workstation to supercomputer and cloud platform. Similarly, we have been able to accelerate NEURONs reaction-diffusion simulation performance through the use of just-in-time compilation. We show that these efforts have led to a growing developer base, a simpler and more robust software distribution, a wider range of supported computer architectures, a better integration of NEURON with other scientific workflows, and substantially improved performance for the simulation of biophysical and biochemical models.

neuroscience↗

Multiscale computer modeling of spreading depolarization in brain slices

Spreading depolarization (SD) is a slow-moving wave of neuronal depolarization accompanied by a breakdown of ion concentration homeostasis, followed by long periods of neuronal silence (spreading depression), and associated with several neurological conditions. We developed multiscale (ions to tissue slice) computer models of SD in brain slices using the NEURON simulator: 36,000 neurons (2 voltage-gated ion channels; 3 leak channels; 3 ion exchangers/pumps) in the extracellular space (ECS) of a slice (1 mm sides, varying thickness) with ion (K+, Cl-, Na+) and O2 diffusion and equilibration with a surrounding bath. Glia and neurons cleared K+ from the ECS via Na+/K+ pumps. SD propagated through the slices at realistic speeds of 2-4 mm/min, which increased by as much as 50% in models incorporating the effects of hypoxia or propionate. In both cases, the speedup was mediated principally by ECS shrinkage. Our model allows us to make testable predictions, including: 1. SD can be inhibited by enlarging ECS volume; 2. SD velocity will be greater in areas with greater neuronal density, total neuronal volume, or larger/more dendrites; 3. SD is all-or-none: initiating K+ bolus properties have little impact on SD speed; 4. Slice thickness influences SD due to relative hypoxia in the slice core, exacerbated by SD in a pathological cycle; 5. SD and high neuronal spike rates will be observed in the core of the slice. Cells in the periphery of the slice near an oxygenated bath will resist SD. SignificanceSpreading depolarization (SD) is a slow moving wave of electrical and ionic imbalances in brain tissue and is a hallmark of several neurological disorders. We developed a multiscale computer model of brain slices with realistic neuronal densities, ions, and oxygenation. Our model shows that SD is exacerbated by and causes hypoxia, resulting in strong SD dependence on slice thickness. Our model also predicts that the velocity of SD propagation is not dependent on its initiation, but instead on tissue properties, including the amount of extracellular space and the total area of neuronal membrane, suggesting faster SD following ischemic stroke or traumatic brain injury.

neuroscience↗

Efficient simulation of 3D reaction-diffusion in models of neurons and networks

Neuronal activity is the result of both the electrophysiology and chemophysiology. A neuron can be well represented for the purposes of electrophysiological simulation as a tree composed of connected cylinders. This representation is also apt for 1D simulations of their chemophysiology, provided the spatial scale is larger than the diameter of the cylinders and there is radial symmetry. Higher dimensional simulation is necessary to accurately capture the dynamics when these criteria are not met, such as with wave curvature, spines, or diffusion near the soma. We have developed a solution to enable efficient finite volume method simulation of reaction-diffusion kinetics in intracellular 3D regions in neuron and network models and provide an implementation within the NEURON simulator. An accelerated version of the CTNG 3D reconstruction algorithm transforms morphologies suitable for ion-channel based simulations into consistent 3D voxelized regions. Kinetics are then solved using a parallel algorithm based on Douglas-Gunn that handles the irregular 3D geometry of a neuron; these kinetics are coupled to NEURONs 1D mechanisms for ion channels, synapses, etc. The 3D domain may cover the entire cell or selected regions of interest. Simulations with dendritic spines and of the soma reveal details of dynamics that would be missed in a pure 1D simulation. We describe and validate the methods and discuss their performance.

neuroscience↗

Pipeline for retrieval of COVID-19 immune signatures

ObjectiveThe accelerating pace of biomedical publication has made retrieving papers and extracting specific comprehensive scientific information a key challenge. A timely example of such a challenge is to retrieve the subset of papers that report on immune signatures (coherent sets of biomarkers) to understand the immune response mechanisms which drive differential SARS-CoV-2 infection outcomes. A systematic and scalable approach is needed to identify and extract COVID-19 immune signatures in a structured and machine-readable format. Materials and MethodsWe used SPECTER embeddings with SVM classifiers to automatically identify papers containing immune signatures. A generic web platform was used to manually screen papers and allow anonymous submission. ResultsWe demonstrate a classifier that retrieves papers with human COVID-19 immune signatures with a positive predictive value of 86%. Semi-automated queries to the corresponding authors of these publications requesting signature information achieved a 31% response rate. This demonstrates the efficacy of using a SVM classifier with document embeddings of the abstract and title, to retrieve papers with scientifically salient information, even when that information is rarely present in the abstract. Additionally, classification based on the embeddings identified the type of immune signature (e.g., gene expression vs. other types of profiling) with a positive predictive value of 74%. ConclusionCoupling a classifier based on document embeddings with direct author engagement offers a promising pathway to build a semistructured representation of scientifically relevant information. Through this approach, partially automated literature mining can help rapidly create semistructured knowledge repositories for automatic analysis of emerging health threats.

immunology↗

Human Neocortical Neurosolver (HNN): A new software tool for interpreting the cellular and network origin of human MEG/EEG data

Magneto- and electro-encephalography (MEG/EEG) non-invasively record human brain activity with millisecond resolution providing reliable markers of healthy and disease states. Relating these macroscopic signals to underlying cellular- and circuit-level generators is a limitation that constrains using MEG/EEG to reveal novel principles of information processing or to translate findings into new therapies for neuropathology. To address this problem, we built Human Neocortical Neurosolver (HNN, https://hnn.brown.edu) software. HNN has a graphical user interface designed to help researchers and clinicians interpret the neural origins of MEG/EEG. HNNs core is a neocortical circuit model that accounts for biophysical origins of electrical currents generating MEG/EEG. Data can be directly compared to simulated signals and parameters easily manipulated to develop/test hypotheses on a signals origin. Tutorials teach users to simulate commonly measured signals, including event related potentials and brain rhythms. HNNs ability to associate signals across scales makes it a unique tool for translational neuroscience research.

neuroscience↗

Open Source Brain: a collaborative resource for visualizing, analyzing, simulating and developing standardized models of neurons and circuits

Computational models are powerful tools for investigating brain function in health and disease. However, biologically detailed neuronal and circuit models are complex and implemented in a range of specialized languages, making them inaccessible and opaque to many neuroscientists. This has limited critical evaluation of models by the scientific community and impeded their refinement and widespread adoption. To address this, we have combined advances in standardizing models, open source software development and web technologies to develop Open Source Brain, a platform for visualizing, simulating, disseminating and collaboratively developing standardized models of neurons and circuits from a range of brain regions. Model structure and parameters can be visualized and their dynamical properties explored through browser-controlled simulations, without writing code. Open Source Brain makes neural models transparent and accessible and facilitates testing, critical evaluation and refinement, thereby helping to improve the accuracy and reproducibility of models, and their dissemination to the wider community.

neuroscience↗