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O'Buckley, T. K.

Publications and source records attributed to O'Buckley, T. K..

2 recordsLinked to original sources

ABEL: an active-learning behavior estimation and labeling platform

Detailed behavior analysis is essential for thorough characterization of ethologically relevant behaviors in model organisms, yet manual annotation of the full behavioral repertoire remains subjective, time intensive, and susceptible to observer error. Advances in machine learning have enabled high-throughput pose estimation on recorded video, but tools for behavior classification from pose and video data are still developing. Instead of hand-scoring every frame of video, experimenters can instead label a small subset of video frames and software trained through machine learning makes predictions on the rest. Here, we present an Active-learning Behavior Estimation and Labeling (ABEL) platform that uses clip-level active learning (i.e., human labeling of short video snippets) with multimodal features (pose, video, context/ROI) to train robust behavior classifiers. We rigorously validated ABEL-derived behavior predictions against expert human observers and field-standard automated software, across diverse rodent behavioral assays. Across eight assays and 45 behaviors, model training required 19.5 hours of human annotation in total, with the reviewer scoring ~8% of available video. Models trained in ABEL achieved a mean precision-recall area under the curve (PR-AUC - a 0-1 score of how well a model balances missed detections against false alarms, with 1 being perfect) of 0.90 (SD 0.09, range 0.60-0.99), with no association between performance and behavior prevalence (r = 0.20). This was aided by custom tools, Essence Extractor and UMAP Interactive Selection, for targeted discovery of high probability clips which reduce the clip review needed to find a rare behavior 6-fold relative to random sampling and 10-fold relative to labeling whole videos. As a biological validation, we assessed how ABEL-derived behaviors relate to underlying neuronal calcium dynamics. Behavior labels were tightly synced with neuronal signatures distinct from ambiguous behavior and randomly chosen, behavior-unrelated time windows (shuffle control). Together, these data indicate that ABEL provides an efficient platform for frame-precise classification of distinct ethologically relevant behaviors.

neuroscience↗

Sex- and Subtype-Specific Adaptations in Excitatory Signaling Onto Deep-Layer Prelimbic Cortical Pyramidal Neurons After Chronic Alcohol Exposure

Long-term alcohol use results in behavioral deficits including impaired working memory, elevated anxiety, and blunted inhibitory control that are associated with prefrontal cortical (PFC) dysfunction. Preclinical observations demonstrate multiple impairments in GABAergic neurotransmission onto deep-layer principal cells (PCs) in prelimbic cortex that suggest dependence-related cortical dysfunction is the product of elevated excitability in these cells. Despite accumulating evidence showing alcohol-induced changes in interneuron signaling onto PCs differ between sexes, there is limited data explicitly evaluating sex-specific ethanol effects on excitatory signaling onto deep-layer PCs that may further contribute to deficits in PFC-dependent behaviors. To address this, we conducted electrophysiological and behavioral tests in both male and female Sprague-Dawley rats to evaluate the effects of chronic ethanol exposure. Among our observations, we report a marked enhancement in glutamatergic signaling onto deep-layer PCs in male, but not female, rats after alcohol exposure. This phenomenon was furthermore specific to a sub-class of PC, sub-cortically projecting Type-A cells, and coincided with enhanced anxiety-like behavior, but no observable deficit in working memory. In contrast, female rats displayed an alcohol-induced facilitation in working memory performance with no change in expression of anxiety-like behavior. Together, these results suggest fundamental differences in alcohol effects on cell activity, cortical sub-circuits, and PFC-dependent behaviors across male and female rats.

neuroscience↗