Different responses of mice and rats hippocampus CA1 pyramidal neurons to in vitro and in vivo-like inputs

Front Cell Neurosci. 2023 Dec 7:17:1281932. doi: 10.3389/fncel.2023.1281932. eCollection 2023.

Abstract

The fundamental role of any neuron within a network is to transform complex spatiotemporal synaptic input patterns into individual output spikes. These spikes, in turn, act as inputs for other neurons in the network. Neurons must execute this function across a diverse range of physiological conditions, often based on species-specific traits. Therefore, it is crucial to determine the extent to which findings can be extrapolated between species and, ultimately, to humans. In this study, we employed a multidisciplinary approach to pinpoint the factors accounting for the observed electrophysiological differences between mice and rats, the two species most used in experimental and computational research. After analyzing the morphological properties of their hippocampal CA1 pyramidal cells, we conducted a statistical comparison of rat and mouse electrophysiological features in response to somatic current injections. This analysis aimed to uncover the parameters underlying these distinctions. Using a well-established computational workflow, we created ten distinct single-cell computational models of mouse CA1 pyramidal neurons, ready to be used in a full-scale hippocampal circuit. By comparing their responses to a variety of somatic and synaptic inputs with those of rat models, we generated experimentally testable hypotheses regarding species-specific differences in ion channel distribution, kinetics, and the electrophysiological mechanisms underlying their distinct responses to synaptic inputs during the behaviorally relevant Gamma and Sharp-Wave rhythms.

Keywords: computational modeling; electrophysiological features; hippocampus; pyramidal neurons; rodent comparison.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research has received funding from the European Union’s Horizon 2020 Framework Program for Research and Innovation under Specific Grant Agreement 945539 (Human Brain Project SGA3); Flag ERA JTC 2019 (MILEDI Project 825207) and from the Italian National Recovery and Resilience Plan (PNRR), M4C2, funded by the European Union – NextGenerationEU (Project IR0000011, CUP B51E22000150006, “EBRAINS-Italy.” (European Brain ReseArch INfrastructureS-Italy). Fenix computing and storage resources under Specific Grant Agreement 800858 (Human Brain Project ICEI), and a grant from the Swiss National Supercomputing Centre (CSCS) under project ID ich002 to MM. AR, MP, and YS were supported by funding to the Blue Brain Project, a research center of the École polytechnique fédérale de Lausanne (EPFL), from the Swiss government’s ETH Board of the Swiss Federal Institutes of Technology.