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Featured researches published by Marco de Curtis.


Progress in Neurobiology | 2011

GABAergic synchronization in the limbic system and its role in the generation of epileptiform activity

Massimo Avoli; Marco de Curtis

GABA is the main inhibitory neurotransmitter in the adult forebrain, where it activates ionotropic type A and metabotropic type B receptors. Early studies have shown that GABA(A) receptor-mediated inhibition controls neuronal excitability and thus the occurrence of seizures. However, more complex, and at times unexpected, mechanisms of GABAergic signaling have been identified during epileptiform discharges over the last few years. Here, we will review experimental data that point at the paradoxical role played by GABA(A) receptor-mediated mechanisms in synchronizing neuronal networks, and in particular those of limbic structures such as the hippocampus, the entorhinal and perirhinal cortices, or the amygdala. After having summarized the fundamental characteristics of GABA(A) receptor-mediated mechanisms, we will analyze their role in the generation of network oscillations and their contribution to epileptiform synchronization. Whether and how GABA(A) receptors influence the interaction between limbic networks leading to ictogenesis will be also reviewed. Finally, we will consider the role of altered inhibition in the human epileptic brain along with the ability of GABA(A) receptor-mediated conductances to generate synchronous depolarizing events that may lead to ictogenesis in human epileptic disorders as well.


Epilepsia Open | 2018

How do we use in vitro models to understand epileptiform and ictal activity? A report of the TASK1-WG4 group of the ILAE/AES Joint Translational Task Force

Chris G. Dulla; Damir Janigro; Premysl Jiruska; Joseph V. Raimondo; Akio Ikeda; Chou Ching K. Lin; Howard P. Goodkin; Aistea S. Galanopoulou; Christophe Bernard; Marco de Curtis

In vitro brain tissue preparations allow the convenient and affordable study of brain networks and have allowed us to garner molecular, cellular, and electrophysiologic insights into brain function with a detail not achievable in vivo. Preparations from both rodent and human postsurgical tissue have been utilized to generate in vitro electrical activity similar to electrographic activity seen in patients with epilepsy. A great deal of knowledge about how brain networks generate various forms of epileptiform activity has been gained, but due to the multiple in vitro models and manipulations used, there is a need for a standardization across studies. Here, we describe epileptiform patterns generated using in vitro brain preparations, focusing on issues and best practices pertaining to recording, reporting, and interpretation of the electrophysiologic patterns observed. We also discuss criteria for defining in vitro seizure‐like patterns (i.e., ictal) and interictal discharges. Unifying terminologies and definitions are proposed. We suggest a set of best practices for reporting in vitro studies to favor both efficient across‐lab comparisons and translation to in vivo models and human studies.


Archive | 2012

Figure 1, Chain reaction

John G. R. Jefferys; Premysl Jiruska; Marco de Curtis; Massimo Avoli


Archive | 2012

Figure 2, IEDs analysed in in vitro models of epileptiform synchronization

Marco de Curtis; John G. R. Jefferys; Massimo Avoli


Archive | 2012

Figure 3, Schematic diagrams to illustrate mechanisms that promote epileptiform synchronization and their broad relationships (left panel in red), and those that reduce epileptiform synchronization (right panel in blue)

John G. R. Jefferys; Premysl Jiruska; Marco de Curtis; Massimo Avoli


Archive | 2012

Figure 6, GABAA receptor function modulates ictal discharges in brain FCD slices

Marco de Curtis; John G. R. Jefferys; Massimo Avoli


Archive | 2012

Figure 4, [A: Effects induced by cutting...].

John G. R. Jefferys; Premysl Jiruska; Marco de Curtis; Massimo Avoli


Archive | 2012

Figure 1, Interictal epileptic discharge (IED) patterns recorded in human partial epilepsies with intracranial electrodes

Marco de Curtis; John G. R. Jefferys; Massimo Avoli


Archive | 2012

Figure 5, Synchronous activity induced by bath application of 4AP in neocortical slices obtained from TLE (i.e., presenting with no architectural anomaly) and FCD patients

Marco de Curtis; John G. R. Jefferys; Massimo Avoli


Archive | 2012

Figure 2, Epileptiform activity recorded in a rodent combined hippocampus-entorhinal cortex slice during continuous application of 4-aminopyridine

John G. R. Jefferys; Premysl Jiruska; Marco de Curtis; Massimo Avoli

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Massimo Avoli

Montreal Neurological Institute and Hospital

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Premysl Jiruska

Charles University in Prague

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Gabriella Panuccio

Sapienza University of Rome

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Giovanni Carriero

Carlo Besta Neurological Institute

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Aistea S. Galanopoulou

Albert Einstein College of Medicine

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Damir Janigro

Case Western Reserve University

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