ArticleJournal of computational neuroscience2015
Examining the limits of cellular adaptation bursting mechanisms in biologically-based excitatory networks of the hippocampus.
Article in Journal of computational neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Modular architecture facilitates noise-driven control of synchrony in neuronal networks.Science advances · 2023Article
- Exact mean-field models for spiking neural networks with adaptation.Journal of computational neuroscience · 2022Article
- A Hypothesis for Theta Rhythm Frequency Control in CA1 Microcircuits.Frontiers in neural circuits · 2021Article
- Understanding the Generation of Network Bursts by Adaptive Oscillatory Neurons.Frontiers in neuroscience · 2018Article
- Different roles for inhibition in the rhythm-generating respiratory network.Journal of neurophysiology · 2017Article
- CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging.PeerJ · 2017Article
- Interaction between synaptic inhibition and glial-potassium dynamics leads to diverse seizure transition modes in biophysical models of human focal seizures.Journal of computational neuroscience · 2016Article
- Combining Theory, Model, and Experiment to Explain How Intrinsic Theta Rhythms Are Generated in aneNeuroArticle
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Authors and funding
5 authors.
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Abstract
Determining the biological details and mechanisms that are essential for the generation of population rhythms in the mammalian brain is a challenging problem. This problem cannot be addressed either by experimental or computational studies in isolation. Here we show that computational models that are carefully linked with experiment provide insight into this problem. Using the experimental context of a whole hippocampus preparation in vitro that spontaneously expresses theta frequency (3-12 Hz) population bursts in the CA1 region, we create excitatory network models to examine whether cellular adaptation bursting mechanisms could critically contribute to the generation of this rhythm. We use biologically-based cellular models of CA1 pyramidal cells and network sizes and connectivities that correspond to the experimental context. By expanding our mean field analyses to networks with heterogeneity and non all-to-all coupling, we allow closer correspondence with experiment, and use these analyses to greatly extend the range of parameter values that are explored. We find that our model excitatory networks can produce theta frequency population bursts in a robust fashion.Thus, even though our networks are limited by not including inhibition at present, our results indicate that cellular adaptation in pyramidal cells could be an important aspect for the occurrence of theta frequency population bursting in the hippocampus. These models serve as a starting framework for the inclusion of inhibitory cells and for the consideration of additional experimental features not captured in our present network models.
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