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An in silico model for determining the influence of neuronal co-activity on rodent spatial behavior.
Srinivasan, Aditya; Srinivasan, Arvind; Riceberg, Justin S; Goodman, Michael R; Guise, Kevin G; Shapiro, Matthew L.
Afiliación
  • Srinivasan A; Department of Neuroscience and Experimental Therapeutics, Albany Medical College, 47 New Scotland Ave, Mail Code 126, Albany, NY 12208, United States. Electronic address: sriniva1@amc.edu.
  • Srinivasan A; Department of Neuroscience and Experimental Therapeutics, Albany Medical College, 47 New Scotland Ave, Mail Code 126, Albany, NY 12208, United States; College of Health Sciences, California Northstate University, 2910 Prospect Park Drive, Rancho Cordova, CA 95670, United States.
  • Riceberg JS; Department of Neuroscience and Experimental Therapeutics, Albany Medical College, 47 New Scotland Ave, Mail Code 126, Albany, NY 12208, United States; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, Hess Center for Science and Medicine, 1470 Madison Avenue, New York, NY 10029, Uni
  • Goodman MR; Department of Neuroscience and Experimental Therapeutics, Albany Medical College, 47 New Scotland Ave, Mail Code 126, Albany, NY 12208, United States.
  • Guise KG; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, Hess Center for Science and Medicine, 1470 Madison Avenue, New York, NY 10029, United States.
  • Shapiro ML; Department of Neuroscience and Experimental Therapeutics, Albany Medical College, 47 New Scotland Ave, Mail Code 126, Albany, NY 12208, United States. Electronic address: shapirm@amc.edu.
J Neurosci Methods ; 377: 109627, 2022 07 15.
Article en En | MEDLINE | ID: mdl-35609789
ABSTRACT

BACKGROUND:

Neuropsychological and neurophysiological analyses focus on understanding how neuronal activity and co-activity predict behavior. Experimental techniques allow for modulation of neuronal activity, but do not control neuronal ensemble spatiotemporal firing patterns, and there are few, if any, sophisticated in silico techniques which accurately reconstruct physiological neural spike trains and behavior using unit co-activity as an input parameter. NEW

METHOD:

Our approach to simulation of neuronal spike trains is based on using state space modeling to estimate a weighted graph of interaction strengths between pairs of neurons along with separate estimations of spiking threshold voltage and neuronal membrane leakage. These parameters allow us to tune a biophysical model which is then employed to accurately reconstruct spike trains from freely behaving animals and then use these spike trains to estimate an animal's spatial behavior. The reconstructed spatial behavior allows us to confirm the same information is present in both the recorded and simulated spike trains.

RESULTS:

Our method reconstructs spike trains (98 ± 0.0013% like original spike trains, mean ± SEM) and animal position (9.468 ± 0.240 cm, mean ± SEM) with high fidelity. COMPARISON WITH EXISTING METHOD(S) To our knowledge, this is the first method that uses empirically derived network connectivity to constrain biophysical parameters and predict spatial behavior. Together, these methods allow in silico quantification of the contribution of specific unit activity and co-activity to animal spatial behavior.

CONCLUSIONS:

Our novel approach provides a flexible, robust in silico technique for determining the contribution of specific neuronal activity and co-activity to spatial behavior.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Roedores / Modelos Neurológicos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Neurosci Methods Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Roedores / Modelos Neurológicos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Neurosci Methods Año: 2022 Tipo del documento: Article