arXiv subjects

Renato Corradetti

Publications and source records attributed to Renato Corradetti.

3 recordsLinked to original sources

arXiv2026

Learning Hippo: Multi-attractor Dynamics and Stability Effects in a Biologically Detailed CA3 Extension of Hopfield Networks

We present a biologically detailed extension of the classical Hopfield/Marr auto-associative memory model for CA3, implementing ten populations (two asymmetric pyramidal subtypes, eight GABAergic interneuron classes), forty-seven compartments, multi-rule plasticity (recurrent Hebb, BCM anti-saturation, mossy-fiber short-term, endocannabinoid iLTD, burst-gated Hebb), and a bimodal cholinergic encoding/consolidation cycle. Evaluated on pattern completion across auto-associative, associative, and temporal regimes, and on a controlled inhibitory-proportion manipulation at $N{=}256$, the full architecture exhibits \emph{three qualitative signatures absent from a minimal Hopfield baseline}: (i)~multi-attractor cross-seed behaviour at $K{=}5$ with biologically realistic inhibitory proportions, where two of five seeds converge to positive attractors with margin ${+}0.10{-}0.22$ (Cohen's $d{=}0.71$, one-sided $p{=}0.08$); (ii)~target-selective associative recall in paired $(A, B)$ memory at $K{\geq}5$, where the full model retrieves $B$ from a partial cue of $A$ while the minimal model echoes $A$ (Pearson margin $\Delta{=}{+}0.163$ at $K{=}5$); (iii)~reduced cross-seed variance of the full model below the minimal baseline under clean upstream, with ratios $1.0{-}3.0$. These three signatures are architecture-specific: they appear consistently across independent regimes and are absent from the minimal control.

cs.NE↗

arXiv2024

Synthetic Data for Discriminating Serotonergic Neurons using Convolutional Neural Networks

Serotonergic neurons in the raphe nuclei exhibit diverse electrophysiological properties and functional roles, yet conventional identification methods rely on restrictive criteria that likely overlook atypical serotonergic cells. The use of convolutional neural network (CNN) for comprehensive classification of both typical and atypical serotonergic neurons is an interesting one, but the key challenge is often given by the limited experimental data available for training. This study presents a procedure for synthetic data generation that combines smoothed spike waveforms with heterogeneous noise masks from real recordings. This approach expanded the training set while mitigating overfitting of background noise signatures. CNN models trained on the augmented dataset achieved high accuracy (96.2% true positive rate, 88.8% true negative rate) on non-homogeneous test data collected under different experimental conditions than the training, validation and testing data.

q-bio.NC↗

arXiv2024

Deep Learning Models for Atypical Serotonergic Cells Recognition

The serotonergic system modulates brain processes via functionally distinct subpopulations of neurons with heterogeneous properties, including their electrophysiological activity. In extracellular recordings, serotonergic neurons to be investigated for their functional properties are commonly identified on the basis of "typical" features of their activity, i.e. slow regular firing and relatively long duration of action potentials. Thus, due to the lack of equally robust criteria for discriminating serotonergic neurons with "atypical" features from non-serotonergic cells, the physiological relevance of the diversity of serotonergic neuron activities results largely understudied. We propose deep learning models capable of discriminating typical and atypical serotonergic neurons from non-serotonergic cells with high accuracy. The research utilized electrophysiological in vitro recordings from serotonergic neurons identified by the expression of fluorescent proteins specific to the serotonergic system and non-serotonergic cells. These recordings formed the basis of the training, validation, and testing data for the deep learning models. The study employed convolutional neural networks (CNNs), known for their efficiency in pattern recognition, to classify neurons based on the specific characteristics of their action potentials.

q-bio.NC↗