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ABSTRACT Achieving targeted perturbations of neural activity is essential for dissecting the causal architecture of brain circuits. A crucial challenge in targeted manipulation experiments is the identification ofhigh efficacyperturbation sites whose stimulation exerts desired effects, currently done with costly trial-and-error procedures. Can one predict stimulation effects solely based on observations of the circuit activity, in the absence of perturbation? We answer this question in dissociated neuronal cultures on High-Density Microelectrode Arrays (HD-MEAs), which, compared toin vivopreparations, offer a controllablein vitroplatform that enables precise stimulation and full access to network dynamics. We first reconstruct theperturbome- the full map of network responses to focal electrical stimulation - by sequentially activating individual single sites and quantifying their network-wide effects. The measured perturbome patterns cluster into functional modules, with limited spread across clusters. We then demonstrate that the perturbome can be predicted from spontaneous activity alone. Using short baseline recordings in the absence of perturbations, we estimate Effective Connectivity (EC) and show that it predicts the spatial organization of the perturbome, including spatial clusters and local connectivity. Our results demonstrate that spontaneous dynamics encode the latent causal structure of neural circuits and that EC metrics can serve as effective, model-free proxies for stimulation outcomes. This framework enables data-driven targeting and causal inferencein vitro, with potential applications to more complex preparations such as human iPSC-derived neurons and brain organoids, with implications for both basic research and therapeutic strategies targeting neurological disorders. Significance StatementNeuronal cultures are increasingly used as controllable platforms to study neuronal network dynamics, neuromodulation, and brain-inspired therapies. To fully exploit their potential, we need robust methods to probe and interpret causal interactions. Here, we develop a framework to reconstruct the perturbome—the network-wide map of responses to localized electrical stimulation—and show that it can be predicted from spontaneous activity alone. Using simple, model-free metrics of Effective Connectivity, we reveal that ongoing activity encodes causal structure and provides reliable proxies for stimulation outcomes. This validates EC as a practical measure of causal influence in vitro. Our methodology refines the use of neuronal cultures for brain-on-a-chip approaches, and paves the way for data-driven neuromodulation strategies in human stem cell–derived neurons and brain organoids.
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Birhythmic Analog Circuit Maze: A Nonlinear Neurostimulation Testbed
Brain dynamics can exhibit narrow-band nonlinear oscillations and multistability. For a subset of disorders of consciousness and motor control, we hypothesized that some symptoms originate from the inability to spontaneously transition from one attractor to another. Using external perturbations, such as electrical pulses delivered by deep brain stimulation devices, it may be possible to induce such transition out of the pathological attractors. However, the induction of transition may be non-trivial, rendering the current open-loop stimulation strategies insufficient. In order to develop next-generation neural stimulators that can intelligently learn to induce attractor transitions, we require a platform to test the efficacy of such systems. To this end, we designed an analog circuit as a model for the multistable brain dynamics. The circuit spontaneously oscillates stably on two periods as an instantiation of a 3-dimensional continuous-time gated recurrent neural network. To discourage simple perturbation strategies, such as constant or random stimulation patterns from easily inducing transition between the stable limit cycles, we designed a state-dependent nonlinear circuit interface for external perturbation. We demonstrate the existence of nontrivial solutions to the transition problem in our circuit implementation.
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- Award ID(s):
- 1845836
- PAR ID:
- 10172511
- Date Published:
- Journal Name:
- Entropy
- Volume:
- 22
- Issue:
- 5
- ISSN:
- 1099-4300
- Page Range / eLocation ID:
- 537
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3390/e22050537
