Abstract

Spontaneous network activity plays a fundamental role in the formation of functional networks during early development. The landmark of this activity is the recurrent emergence of intensive time-limited network bursts (NBs) rapidly spreading across the entire dissociated culture in vitro. The main excitatory mediators of NBs are glutamatergic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) and N-Methyl-D-aspartic-acid receptors (NMDARs) that express fast and slow ion channel kinetics, respectively. The fast inhibition of the activity is mediated through gamma-aminobutyric acid type A receptors (GABAARs). Although the AMPAR, NMDAR and GABAAR kinetics have been biophysically characterized in detail at the monosynaptic level in a variety of brain areas, the unique features of NBs emerging from the kinetics and the complex interplay of these receptors are not well understood. The goal of this study is to analyze the contribution of fast GABAARs on AMPAR- and NMDAR- mediated spontaneous NB activity in dissociated neonatal rat cortical cultures at 3 weeks in vitro. The networks were probed by both acute and gradual application of each excitatory receptor antagonist and combinations of acute excitatory and inhibitory receptor antagonists. At the same time, the extracellular network-wide activity was recorded with microelectrode arrays (MEAs). We analyzed the characteristic NB measures extracted from NB rate profiles and the distributions of interspike intervals, interburst intervals, and electrode recruitment time as well as the similarity of spatio-temporal patterns of network activity under different receptor antagonists. We show that NBs were rapidly initiated and recruited as well as diversely propagated by AMPARs and temporally and spatially maintained by NMDARs. GABAARs reduced the spiking frequency in AMPAR-mediated networks and dampened the termination of NBs in NMDAR-mediated networks as well as slowed down the recruitment of activity in all networks. Finally, we show characteristic super bursts composed of slow NBs with highly repetitive spatio-temporal patterns in gradually AMPAR blocked networks. To the best of our knowledge, this study is the first to unravel in detail how the three main mediators of synaptic transmission uniquely shape the NB characteristics, such as the initiation, maintenance, recruitment and termination of NBs in cortical cell cultures in vitro.

Highlights

  • Spontaneous network activity plays a fundamental role in the formation of functional networks during early development of the central nervous system (Feller, 1999; O’Donovan, 1999; BenAri, 2001; Blankenship and Feller, 2010; Egorov and Draguhn, 2013; Luhmann et al, 2016)

  • The data studied in this work spontaneously exhibit stereotypical network bursting (NB), the periods of intensive activity engaging the majority of neurons and followed by longer silent periods of sparse activity of single spikes

  • We systematically analyzed the unique features of NBs, including the initiation, maintenance, propagation and termination of NBs, which emerge from a complex interplay between fast alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and slow N-Methyl-D-aspartic acid (NMDA) glutamatergic and fast GABAA gabaergic receptors when embedded into a self-organized network

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Summary

Introduction

Spontaneous network activity plays a fundamental role in the formation of functional networks during early development of the central nervous system (Feller, 1999; O’Donovan, 1999; BenAri, 2001; Blankenship and Feller, 2010; Egorov and Draguhn, 2013; Luhmann et al, 2016). Considering that the bursting dynamics are an essential feature of the activity both in vivo and in vitro and that the complex underlying mechanisms that shape this activity are not well understood, their better characterization is highly important. Since in vitro networks are easy to control under several pharmacological conditions with simultaneous long-term recordings of the evolution of the extracellular network-wide activity with microelectrode arrays (MEAs), they provide a model system that helps to unravel and compare the receptor mechanisms that modulate the dynamics of cortical circuits in vivo. In this work we study how the spontaneous NBs are shaped by the underlying interplay of the excitatory and inhibitory receptors of synaptic transmission to modify excitation-inhibition balance in dissociated in vitro cultures extracted from both hemispheres of postnatal (P0) rats. The goal of the study is to analyze the contribution of fast gamma-aminobutyric acid type A receptors (GABAARs) on alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic

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