Muhammad, Naseer (2026) Mathematical Modeling of Neuronal Dynamics And Population Heterogeneity For Large-Scale Neuronal Networks. [Tesi di dottorato]
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| Tipologia del documento: | Tesi di dottorato |
|---|---|
| Lingua: | English |
| Titolo: | Mathematical Modeling of Neuronal Dynamics And Population Heterogeneity For Large-Scale Neuronal Networks |
| Autori: | Autore Email Muhammad, Naseer muhammad.naseer@unina.it |
| Data: | 10 Febbraio 2026 |
| Numero di pagine: | 85 |
| Istituzione: | Università degli Studi di Napoli Federico II |
| Dipartimento: | Matematica e Applicazioni "Renato Caccioppoli" |
| Dottorato: | Matematica e Applicazioni |
| Ciclo di dottorato: | 38 |
| Coordinatore del Corso di dottorato: | nome email Carlo, Nitsch carlo.nitsch@unina.it |
| Tutor: | nome email Addolorata, Marasco [non definito] |
| Data: | 10 Febbraio 2026 |
| Numero di pagine: | 85 |
| Parole chiave: | Mathematical modeling; Neuronal dynamics; Large-scale neuronal networks |
| Settori scientifico-disciplinari del MIUR: | Area 01 - Scienze matematiche e informatiche > MAT/07 - Fisica matematica |
| Informazioni aggiuntive: | My Phd cycle is 38, but its not here in the list of Phd cycle. |
| Depositato il: | 17 Giu 2026 21:02 |
| Ultima modifica: | 12 Ago 2026 05:37 |
| URI: | https://www.fedoa.unina.it/id/eprint/16216 |
Abstract
This thesis develops and evaluates a data-driven modeling framework for reproducing the firing behavior of hippocampal CA1 pyramidal neurons using the Adaptive Generalized Leaky Integrate-and-Fire (A-GLIF) model. The framework was applied to whole-cell patch-clamp recordings from 109 neurons obtained from GFP-expressing mice, wild-type Control mice, WT-Volkmar mice, and APPPS1 transgenic mice. A-GLIF parameters were individually fitted for each neuron, and model performance was validated by comparing experimental and simulated spike trains across multiple stimulation currents. Mann–Whitney U-tests revealed no statistically significant differences in spike timing (p > 0.05), indicating strong agreement between recorded and simulated activity. Model accuracy was further quantified using the Spike Train Similarity Measure (STSimM), which consistently demonstrated high temporal accuracy (≥ 70%) and F-scores (≥ 60%). The fitted models were subsequently used to reconstruct missing stimulation ranges, providing initial estimates of permissible firing boundaries and spike-time variability. Based on these estimates, heterogeneous neuron populations for all groups were generated by perturbing 12 key A-GLIF parameters. To ensure biological plausibility, only neuron copies whose firing patterns remained within experimentally observed variability envelopes were retained. Overall, this work presents a computationally efficient and biologically grounded approach for generating realistic neuronal populations, enabling scalable and physiologically consistent large-scale simulations, while also providing insight into excitability alterations associated with Alzheimer’s disease.
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