Abstract

The ventral midbrain supports a variety of functions through the heterogeneity of neurons. Dopaminergic and GABA neurons within this region are particularly susceptible targets of amphetamine-class psychostimulants such as methamphetamine. While this has been evidenced through single-neuron methods, it remains unclear whether and to what extent the local neuronal network is affected and if so, by which mechanisms. Both GABAergic and dopaminergic neurons were heavily featured within the primary ventral midbrain network model system. Using spontaneous calcium activity, our data suggest methamphetamine decreased total network output via a D2 receptor-dependent manner. Over culture duration, functional connectivity between neurons decreased significantly but was unaffected by methamphetamine. However, across culture duration, exposure to methamphetamine significantly altered changes in network assortativity. Here we have established primary ventral midbrain networks culture as a viable model system that reveals specific changes in network activity, connectivity, and topology modulation by methamphetamine. This network culture system enables control over the type and number of neurons that comprise a network and facilitates detection of emergent properties that arise from the specific organization. Thus, the multidimensional properties of methamphetamine can be unraveled, leading to a better understanding of its impact on the local network structure and function.

Highlights

  • The ventral midbrain neurons are one of the main targets of amphetamines

  • This study is aimed to uncover the mechanisms by which the functional connectivity and structure of cultured GABAergic networks is modulated by methamphetamine

  • Clustering coefficient extends upon pair-wise correlations by determining the fraction of complete triangular connections around a neuron

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Summary

Introduction

The ventral midbrain neurons are one of the main targets of amphetamines. Amphetamineclass drugs have been shown to increase extracellular dopamine levels by stimulation of firing activity of dopamine neurons and via stimulation of dopamine efflux through the dopamine transporter [1]. Once in the extracellular space, dopamine rapidly diffuses from the site of release and acts upon both pre- and postsynaptic receptors [2,3,4]. Activation of presynaptic D2 receptors in turn decreases firing activity of dopaminergic neurons and activation of postsynaptic D2 receptors decreases postsynaptic neuronal activity [5].

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