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Articles, Systems/Circuits

Synchronous Inhibitory Potentials Precede Seizure-Like Events in Acute Models of Focal Limbic Seizures

Laura Uva, Gian Luca Breschi, Vadym Gnatkovsky, Stefano Taverna and Marco de Curtis
Journal of Neuroscience 18 February 2015, 35 (7) 3048-3055; DOI: https://doi.org/10.1523/JNEUROSCI.3692-14.2015
Laura Uva
1Unit of Epileptology and Experimental Neurophysiology, Fondazione Istituto Neurologico Carlo Besta, 20133 Milano, Italy, and
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Gian Luca Breschi
2Department of Neuroscience and Brain Technologies, Italian Institute of Technology, 16163 Genova, Italy
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Vadym Gnatkovsky
1Unit of Epileptology and Experimental Neurophysiology, Fondazione Istituto Neurologico Carlo Besta, 20133 Milano, Italy, and
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Stefano Taverna
2Department of Neuroscience and Brain Technologies, Italian Institute of Technology, 16163 Genova, Italy
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Marco de Curtis
1Unit of Epileptology and Experimental Neurophysiology, Fondazione Istituto Neurologico Carlo Besta, 20133 Milano, Italy, and
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Abstract

Interictal spikes in models of focal seizures and epilepsies are sustained by the synchronous activation of glutamatergic and GABAergic networks. The nature of population spikes associated with seizure initiation (pre-ictal spikes; PSs) is still undetermined. We analyzed the networks involved in the generation of both interictal and PSs in acute models of limbic cortex ictogenesis induced by pharmacological manipulations. Simultaneous extracellular and intracellular recordings from both principal cells and interneurons were performed in the medial entorhinal cortex of the in vitro isolated guinea pig brain during focal interictal and ictal discharges induced in the limbic network by intracortical and brief arterial infusions of either bicuculline methiodide (BMI) or 4-aminopyridine (4AP). Local application of BMI in the entorhinal cortex did not induce seizure-like events (SLEs), but did generate periodic interictal spikes sensitive to the glutamatergic non-NMDA receptor antagonist DNQX. Unlike local applications, arterial perfusion of either BMI or 4AP induced focal limbic SLEs. PSs just ahead of SLE were associated with hyperpolarizing potentials coupled with a complete blockade of firing in principal cells and burst discharges in putative interneurons. Interictal population spikes recorded from principal neurons between two SLEs correlated with a depolarizing potential. We demonstrate in two models of acute limbic SLE that PS events are different from interictal spikes and are sustained by synchronous activation of inhibitory networks. Our findings support a prominent role of synchronous network inhibition in the initiation of a focal seizure.

  • acute seizure model
  • entorhinal cortex
  • focal seizures
  • in vitro guinea pig brain
  • interictal spikes
  • pre-ictal spikes

Introduction

Epileptiform interictal spikes (ISs) in models of focal seizures and of chronic epilepsy correlate with an intracellular pattern defined as paroxysmal depolarizing shift (PDS; Matsumoto and Ajmone-Marsan, 1964), which is characterized by a sequence of fast action potentials superimposed to a slow depolarization (de Curtis and Avanzini, 2001). In limbic and olfactory cortices, ISs induced by pharmacological manipulations are sustained by the activation of synchronous glutamatergic networks (Hoffman and Haberly, 1991; de Curtis et al., 1999; Avoli et al., 2002). In the presence of glutamate receptor antagonists, GABAA-receptor-mediated ISs have been observed in in vitro models of seizure-like events (SLEs) induced by applications of 4-aminopyridine (4AP; Michelson and Wong, 1991; Perreault and Avoli, 1992; Uva et al., 2009), carbachol (Dickson and Alonso, 1997), and GABAB receptor antagonists (Uusisaari et al., 2002). Moreover, the GABAA receptor antagonist bicuculline abolished spontaneous ISs recorded on postsurgical, in vitro brain slices of subiculum and in CA2 hippocampal regions obtained from patients with focal drug-resistant temporal lobe epilepsy (Huberfeld et al., 2007; Wittner et al., 2009). These data demonstrate that both glutamatergic and GABAergic networks can independently sustain epileptiform spikes in different experimental conditions.

The involvement of inhibitory networks at seizure onset is supported by experimental and clinical evidence (de Curtis and Gnatkovsky, 2009; Avoli and de Curtis, 2011). Inhibitory neuron discharges during the transition into a focal seizure were demonstrated in experimental studies performed on in vitro models of SLEs (Avoli, 1990, 1996; Lopantsev and Avoli, 1998; Derchansky et al., 2008; Ziburkus et al., 2006; Gnatkovsky et al., 2008; Lasztoczi et al., 2009; Fujiwara-Tsukamoto et al., 2010). GABAA-mediated synchronization promotes SLEs in postsurgical slices obtained from patients with focal cortical dysplasia treated with 4AP (D'Antuono et al., 2004). In vivo unit recordings in a model of temporal lobe epilepsy demonstrated that principal neurons reduce their firing at the beginning of a seizure whereas interneuron activity increases (Grasse et al., 2013). A reduction of principal neurons firing suggestive of an inhibitory activity during the transition into seizure was also demonstrated with unit recordings performed in the course of presurgical monitoring with intracerebral microelectrodes in patients candidate to epilepsy surgery (Truccolo et al., 2011; Schevon et al., 2012).

The hypothesis that inhibitory network activation sustains seizure onset via the generation of pre-ictal spikes (PSs) is verified here during SLEs induced by two different pharmacological manipulations in the isolated guinea pig brain maintained in vitro. The network determinants of ictogenesis in the limbic region of this close-to-in vivo preparation have been studied extensively (de Curtis et al., 1994; Uva et al., 2005; Gnatkovsky et al., 2008; Trombin et al., 2011; Boido et al., 2014).

Materials and Methods

Brains of adult female Hartley guinea pigs (150–200 g; Charles River) were isolated and maintained in vitro according to the standard procedure described previously (de Curtis et al., 1991; Mühlethaler et al., 1993; de Curtis et al., 1998b). Briefly, the animals were anesthetized with sodium thiopental (125 mg/kg, i.p., Farmotal; Pharmacia) and were transcardially perfused with a cold (10°C), carboxygenated (95% O2/5% CO2) solution containing the following (in mm): 126 NaCl, 3 KCl, 1.2 KH2PO4, 1.3 MgSO4, 2.4 CaCl2, 26 NaHCO3, 15 glucose, and 2.1 HEPES and 3% dextran molecular weight 70,000, pH adjusted at 7.1 with HCl. After decapitation, brains were isolated and transferred into a recording chamber. A cannula was inserted in the basilar artery and brain perfusion with the solution mentioned above (7 ml/min, pH 7.3, 15°C) was restored via a peristaltic pump (Minipulse 3; Gilson). Before starting the electrophysiological experiment, the temperature of both the perfusate and the chamber was slowly (0.2°C/min) raised to 32°C by a temperature controller (PTC 10; NPI).

Extracellular recordings were performed in the medial entorhinal cortex (EC) using 0.9 m NaCl-filled glass pipettes (5–10 MΩ resistance) at 300–500 μm in depth. EC responses evoked by electrical stimulation of the lateral olfactory tract (LOT) through an isolation unit driven by a pulse generator (Telefactor S88; Grass Instruments) were used to monitor the viability of the preparation during the experiment (Biella and de Curtis, 2000). Field potential signals were amplified with a multichannel differential amplifier (Biomedical Engineering) in quasi-DC mode (0.05 Hz high-pass filter). Intracellular recordings in the EC were performed with sharp glass micropipette containing 2 m potassium acetate (input resistance: 60–120 MΩ). Signals recorded with an intracellular bridge amplifier (Neuro Data Instruments) were digitized via an AT-MIO-64E3 National A/D Board (National Instruments) and analyzed with custom-made software (ELPHO) developed in Labview by Dr. Vadym Gnatkovsky.

Epileptiform activities were induced by: (1) local intracortical application of the GABAA receptor antagonist bicuculline methiodide (BMI; Tocris Bioscience; 1–2 mm in 0.9 M sodium chloride) in the EC through an injection pipette (tip diameter 10 μm) connected to a pulse-delivery controlled system (Picospritzer II; Parker Instrumentation); (2) brief arterial application of BMI (50 μm; 3 min perfusions); and (3) arterial application of the K+ channel blocker, 4AP (50 μm; 4 min perfusions; Fluka). Local intracortical application of the non-NMDA receptors antagonist DNQX (2 mm; Abcam) was performed using a Picospritzer.

Two-sample t test was implemented to evaluate the effect of local DNQX application on BMI-induced spikes in 2 portions of EC >2 mm apart. For each test, after DNQX injection, the amplitude of the spikes was measured at the site of BMI injection (EC 1) and at the site of local DNQX injection (EC 2), the mean of the EC 1 and EC 2 spike amplitudes was calculated for each test (n = 9) and the t test was performed comparing the means of EC 1 and EC 2 obtained from 5 to 10 couples of spikes for each test. Arterial applications of DNQX were performed dissolving DNQX in the perfusate (50 μm) and the efficacy of the DNQX block was verified by evaluating the LOT-evoked response.

The number of animals used for the study was minimized according to the international guidelines on ethical use of animals [European Communities Council Directive of 24 November 1986 (86/109/EEC)]. The experimental protocol was reviewed and approved by the Committee on Animal Care and Use and by the Ethics Committee of the Fondazione Istituto Neurologico.

Results

Local injections of BMI (1–2 mm) in the EC (n = 33) generated ISs (Fig. 1) lasting 1128 ± 413 ms (mean ± SD) and recurring at 0.05–0.2 Hz. The periodic IS pattern observed during local BMI application never evolved into SLEs. Intracellular recordings demonstrated that the ISs induced by local BMI corresponded to a depolarizing potential superimposed to a burst of spikes (n = 21); action potential firing was abolished by intracellular injection of negative current that enhanced the amplitude of the underlying depolarizing potential (n = 7; Fig. 1A). Local EC injection of 2 mm DNQX (site EC 2 in Fig. 1B) determined a statistically significant decrease in IS amplitude (amplitude decrease to 73.6 ± 26.4%) compared with EC regions remote to DNQX application where an increase of the ISs amplitude was observed (amplitude increase to 127.4 ± 20.4%; n = 9; 2-sample t test, p-values for all tests were <0.005). The complete abolition of the recorded spikes was not achieved in EC 2 because of the small area of action of DNQX compared with the whole extension of the EC. BMI-induced ISs were completely abolished by arterial application of 50 μm DNQX (n = 4; Fig. 1C) and recovered by 90 min of washout repeating local BMI injections (Fig. 1C, bottom trace). These data suggest that activation of the excitatory glutamatergic circuit is required for the generation of ISs induced by local BMI injection in the EC.

Figure 1.
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Figure 1.

Local application of BMI (1–2 mm) in EC induced glutamatergic spikes. A, Example of ISs recorded in EC after local injection of BMI (bottom traces) and its intracellular correlate (top traces) showing the depolarization and firing of the cell at rest (black trace; resting membrane potential: −69 mV) blocked by hyperpolarizing current injection (gray traces). B, Top, Schematic drawing of the isolated guinea pig brain showing the position of the injecting-pipette-recording electrodes in the EC. As shown at the bottom, ISs were induced in both EC 1 and EC 2 by local application of BMI in EC 1. In EC 2, a decrease in amplitude of the spikes was observed after application of the non-NMDA glutamate receptor blocker DNQX (2 mm). The difference between EC 1 and EC 2 spike amplitude was statistically significant (t test; p = 2.3E-7; DF = 8.80). C, Top, Local injection of BMI-induced ISs. Middle. When 50 μm DNQX was arterially perfused for 45 min, local injection of BMI failed in generating ISs. Bottom, After 90 min washout, BMI local injection was successful in inducing ISs.

When BMI (50 μm) was arterially perfused for 3 min in the isolated guinea pig brain, population spikes transiently appeared in EC (Uva et al., 2005; Gnatkovsky et al., 2008; data not shown) and preceded the generation of SLEs (Librizzi and de Curtis, 2003). As demonstrated previously, brief application of 50 μm BMI causes a reduction of GABAA transmission of ∼30%, thus leaving the GABAA system partially operative (Gnatkovsky et al., 2008). As for BMI, arterial perfusion of 50 μm 4AP induced SLEs preceded by PSs (Fig. 2A; n = 50).

Figure 2.
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Figure 2.

Transition to ictal discharge in EC principal neurons and interneurons. Arterial application of proconvulsant compounds induces PSs and ictal activity in EC. A, Top, intracellular and extracellular activities during PSs and SLE onset induced by arterial application of (4AP; 50 μm; 4 min). The cell membrane was artificially depolarized at −40 mV (rmp: −74 mV). B, Example of two PSs (*) that correlate with membrane potential hyperpolarization. Left, Intracellular LOT-evoked potentials recorded at different cell membrane levels (top) demonstrate the presence of an IPSP with a reversal peak potential similar to the hyperpolarizing potential associated to PSs observed in A and B (in the middle and right, see also Gnatkovsky et al., 2006). The corresponding field potential is shown below each trace. C, Average IPSP amplitudes measured at different membrane potentials (MP) are plotted in the diagram. The EREV −59.3 ± 3.4 mV (n = 11 cells) is extrapolated from the point where the gray line intersects the y-axis (mean ± SD). D, Left, Top, Intracellular activity of a putative interneuron and correlated extracellular activity (bottom traces) after arterial application of 4AP (50 μm; 4 min). Right, Activity recorded at the seizure onset is enlarged to show the intense discharge of the interneuron (rmp: −53 mV). Left, Typical high-frequency firing during depolarizing pulse is illustrated. Right insert, Typical interneuron bursting response to LOT stimulation is shown (see also Gnatkovsky et al., 2007).

Intracellular recordings from both superficial and deep principal EC cells (n = 21 in BMI; rmp: −58.3 ± 7.3 mV; n = 22 in 4AP; rmp: −73.9 ± 1.6 mV; mean ±SD) demonstrated that PSs correlated with an inhibitory potential in 33 neurons (35 seizures, 16 in BMI and 19 in 4AP; see Fig. 4A), a few-millivolt depolarization without firing in 6 neurons (4 in BMI and 2 in 4AP; see Fig. 4A), and a burst of action potentials in 4 principal cells (3 in BMI and 1 in 4AP; see Fig. 4A). Intracellular activity showed a PS-associated putative IPSP (Fig. 2A,B) peaking at −65.4 ± 7.4 mV (mean ± SD) during 4AP application and −66.8 ± 7.3 mV during BMI application (Fig. 3). In all (n = 20) but three principal neurons, ISs that occurred at the end or between two SLEs correlated at the intracellular level with a spike or a burst of action potentials superimposed to a paroxysmal depolarizing shift (Fig. 3). These data demonstrate that, in the same principal neuron, spike events occurring just before (pre-ictal) and after a SLE (between two SLEs) were correlated with inhibitory and depolarizing potentials, respectively. The small depolarizing hump seldom recorded before the IPSPs (Fig. 2Bb) was interpreted either as an excitatory PSP or as a passive membrane potential oscillation.

Figure 3.
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Figure 3.

Simultaneous intracellular (top) and extracellular (bottom) recordings performed during a SLE (left and middle) and between two SLEs (right panel) induced by arterial perfusion of 50 μm BMI. In the middle panel, the bursting activity observed during the late phase of the SLE is shown. In the bottom panels, the correlates of PSs (a) and interictal spikes (b) are illustrated as expanded traces (in the outlined boxes).

The mean duration of the PSs was 382.2 ± 139.7 ms in BMI and 184.8 ± 19.7 ms in 4AP (mean ± SD). We analyzed the firing rate before and after 80 PSs in 13 principal neurons (6 during BMI and 7 in 4AP) with background firing activity before seizure initiation. The averaged firing frequency in the 380 ms (in BMI) and 180 ms (in 4AP) before a PS was 11.5 ± 7.1 Hz. This firing frequency measured before a PS decreased to 0.6 ± 0.8 Hz during the PSs (Fig. 4B, left; mean ± SD).

Figure 4.
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Figure 4.

A, Quantification of the different intracellular correlates of principal cells (left) and interneurons (right) during PSs induced by arterial application of BMI or 4AP. B, Box plots showing the firing frequencies of principal cells (left) and interneurons (right) before and during PSs, represented by white and gray boxes, respectively. The box ranges indicate the 25th and 75th percentile and the whiskers the SD values. Typical intracellular and extracellular activities recorded during PSs in principal cells and interneurons are illustrated in the top inserts. Note that, with the exception of cells 2 and 10, firing rate of principal neurons during PS is decreased to zero.

Putative interneurons identified by neurophysiological criteria (spike rate, firing accommodation, and response to LOT stimulation; Gnatkovsky et al., 2007) recorded after application of BMI and 4AP (n = 3 and n = 1, respectively) generated bursting activity during the PSs (Figs. 2D, 4A). In these 4 putative interneurons, the background firing rate was 13.4 ± 21.8 Hz and increased to 166.2 ± 78.4 Hz during 14 PSs (Fig. 4B, right; mean ± SD). We analyzed separately the correlation between the amplitude of individual PSs and the firing frequency of the interneurons and found a high correlation between these two parameters (r2 > 0.8 in all experiments; Fig. 5). Altogether, these data suggest that, in both 4AP- and BMI-induced epileptogenesis, PSs are associated with IPSPs recorded in principal neurons and generated by spontaneous, burst-like firing activity in interneurons.

Figure 5.
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Figure 5.

Relationship between the firing rate of the four putative interneurons and the amplitudes of extracellular PSs induced by BMI or 4AP administration. Four to eight PSs of different amplitudes were analyzed for each interneuron represented by different symbols. Regression lines and the corresponding correlation coefficients (r2) values are reported for each interneuron.

Discussion

We analyzed population spikes generated in the EC of the isolated guinea pig brain by two different epileptogenic compounds: the GABAA receptor antagonist BMI and the K+ channel blocker 4AP. Regardless of their different mechanisms of action, both drugs induced similar ictal patterns in the temporal/limbic region (Librizzi and de Curtis, 2003; Carriero et al., 2010; Boido et al., 2014) that resemble seizures recorded with intracerebral electrodes in patients with mesial temporal lobe epilepsy (TLE; Engel, 1990; Wendling et al., 2012) and in animal models of mesial TLE (Bragin et al., 1999; Carriero et al., 2012). SLEs induced by arterially applied BMI in the intact brain in vitro initiates with fast activity in the β range (20–30 Hz), followed by irregular spiking and periodic bursting (Uva et al., 2005; Gnatkovsky et al., 2008; Trombin et al., 2011) restricted to the hippocampal and parahippocampal areas (Uva et al., 2005) with a different involvement of subregions during SLE phases (Boido et al., 2014). A similar sequence of ictal events was observed in the isolated guinea pig brain perfused with 4AP via the arterial system (Carriero et al., 2010).

As for human mesial TLE (Bragin et al., 2005; Wendling et al., 2005), PSs initiate both 4AP- and BMI-induced SLEs. These PSs are legitimate ictal events because they were observed exclusively in coincidence with seizure onset. We demonstrate in two different models of SLE that PSs are sustained by network mechanisms different from ISs recorded in the same regions. In the large majority of EC neurons after both BMI and 4AP application, PSs correlated with inhibitory potentials and with the blockade of firing in principal neurons. Because pharmacological manipulations during the few tens of seconds that precede a randomly occurring SLE is not feasible, to understand the nature of PSs, we compared the PS-associated potential with the IPSPs evoked in the same neuron by stimulation of the LOT before the application of the proconvulsive drug. We previously demonstrated that LOT stimulation induces a polisynaptic response in layer II and III neurons of the EC that is mediated by a feedforward GABAergic IPSP (Gnatkovsky and de Curtis, 2006). The reversal potential of LOT-induced IPSP in EC neurons was ∼−67 mV and correlated with the maximal hyperpolarizing deflection observed in EC neurons during PSs. These data are confirmed in neurons in which membrane potential was modified by intracellular current injection during PSs and SLE occurrence. The presence of an inhibitory hyperpolarizing potential during the PS was further confirmed by the demonstration that neuronal firing was abolished in 33 of 43 principal neurons during both in BMI- and 4AP-induced PSs. Moreover, putative interneurons identified by neurophysiological criteria (Gnatkovsky et al., 2007) recorded during the PSs at the onset of BMI- and 4AP-induced SLE showed a bursting discharge, suggesting that IPSPs recorded in principal neurons are due to increased activity of local circuit inhibitory cells. These findings acquire a particular significance for the understanding of human focal epilepsy in the light of the recent demonstration of a reduced unit activity at seizure onset in humans (Truccolo et al., 2011; Schevon et al., 2012) and in epilepsy animal models (Grasse et al., 2013).

In rat slices bathed in 4AP, population spikes sustained exclusively by GABAergic networks have been demonstrated in hippocampus (Avoli, 1990; Perreault and Avoli, 1992) and EC (Lopantsev and Avoli, 1998; Avoli and de Curtis, 2011). Similarly, when glutamatergic transmission was blocked during arterial administration of 4AP in the isolated guinea pig brain, GABAA-mediated synchronous potentials were uncovered (Uva et al., 2009). These GABAergic spikes correlated with membrane hyperpolarization in principal EC neurons and were blocked by BMI. In these conditions of blockade of excitatory transmission, GABAergic spikes were not sufficient to generate SLEs (Uva et al., 2009). Similar network events could subtend PSs.

We hypothesize that 4AP generates GABAergic PSs by enhancing spontaneous interactions predominantly within inhibitory networks. 4AP blockade of repolarizing potassium conductance may elongate action potential repolarization in presynaptic terminals, thus reinforcing synaptic release at inhibitory synapses. GABAergic spikes during the BMI incomplete impairment of GABAa receptor function (see Fig. 1 in Gnatkovsky et al., 2008) could be due to a reduction of interneuron-to-interneuron inhibition. These two hypothetical mechanisms could promote inhibitory network synchronization underlying PSs.

Enhanced inhibitory neuron activity preceding SLE onset have been also documented in rat and mouse cortical brain slices (Trevelyan et al., 2006; Ziburkus et al., 2006; Cammarota et al., 2013). Such inhibitory network activation has been interpreted as a hyperpolarizing wave of inhibition that entrains interneuronal networks to confine the spreading of ictal activity. In another study, it has been proposed that ictal activity occurs when excitatory inputs overcome the inhibitory drive (Derchansky et al., 2008). All of these studies present a conventional interpretation of the phenomenon (i.e., activation of GABAergic cells has an inhibitory function) and do not consider the possibility that increased interneuronal network activity just ahead of a focal seizure could be directly responsible for seizure precipitation.

The role of GABAergic networks in promoting SLEs in EC has been proposed by experiments conducted on hippocampal-entorhinal slices (Avoli, 1996; Lopantsev and Avoli, 1998 Fujiwara-Tsukamoto et al., 2006; Köhling et al., 2000; Ziburkus et al., 2006; see for review de Curtis and Gnatkovsky, 2009; Fujiwara-Tsukamoto et al., 2010; Avoli and de Curtis, 2011). In the rat and human neocortex perfused with 4AP, ictal discharges are initiated by GABAA receptor activation (Avoli et al., 1996; D'Antuono et al., 2004). In rat brain slices exposed to 4AP or 0 mm Mg2+, GABAA-mediated spikes or oscillations anticipating the ictal discharge were recorded and the interference with GABAA transmission determined their abolition together with ictal discharge suppression (Avoli, 1996; Köhling et al., 2000). The progression of a seizure from the initial enhanced inhibitory network activity is presumably mediated either by an increase in extracellular K+ associated with interneuronal activity (Avoli, 1996; D'Antuono et al., 2004; Trombin et al., 2011) or by an excitatory rebound caused by the synchronous inhibition (Cobb et al., 1995; Wendling et al., 2002).

Because arterial application of both BMI and 4AP did not induce sustained ISs in the limbic region, we studied ISs induced by local intracortical application of BMI. As for the olfactory cortex of the isolated guinea pig brain (de Curtis et al., 1994; de Curtis et al., 1998a; de Curtis et al., 1999), this procedure promoted periodic interictal spiking in the EC, but never generated SLEs. It is well known that the direct local injection of BMI (and other convulsants) into the cortex in vivo generates large interictal events that periodically recur, but fails to induce seizures (Prince and Wilder, 1967; Ma et al., 2004). Previous findings obtained in the olfactory cortex of the isolated guinea pig brain strongly suggested that BMI- or picrotoxin-induced ISs are generated by a transient and brief synchronization of excitatory circuits, followed by synchronization of inhibition possibly mediated by intrinsic K+ conductances and GABAB receptor activation that prevents seizure precipitation (de Curtis et al., 1998a). The intracellular activity pattern associated to ISs in the piriform cortex (de Curtis et al., 1998a; de Curtis et al., 1999) was confirmed for the EC in the present report. ISs induced by local BMI application in the EC corresponded to a long-lasting membrane depolarization coupled to the discharge of a burst of action potentials. We demonstrated that these ISs are sustained by glutamatergic networks because they were blocked by the non-NMDA glutamate receptor blocker DNQX (see also de Curtis et al., 1999). Local DNQX was associated with an increase in the amplitude of ISs recorded at a distance from its application. This could be due to the natural evolution of ISs that progressively become larger to reach a plateau amplitude; this increase is blocked at the site of DNQX action. Alternatively, DNQX could block recurrent excitation on remotely acting interneurons, thus reducing inhibition in principal cells out of the area of DNQX influence.

We confirmed that ISs induced by local drug applications and ISs observed between two seizures in our experimental conditions correlate with a PDS (Ayala et al., 1973; Traub and Wong, 1982) mediated by activation of glutamate receptors, as was demonstrated previously in slices of hippocampus (Stanton et al., 1987), neocortex (Hablitz, 1984; Hwa and Avoli, 1991), piriform cortex (Hoffman and Haberly, 1991; Forti et al., 1997), and EC (Jones and Heinemann, 1988).

In conclusion, local activation of the EC with proconvulsive drugs abolishes GABAergic transmission and generates PDS-associated glutamatergic ISs that recur but do not evolve into seizure-like activity. Conversely, brief arterial administration of BMI or 4AP induces a strong activation and synchronization of GABAergic circuits that generate PSs consistently developing into SLEs. These results support the concept that GABAergic circuit synchronization plays a pivotal role in the initiation of focal epileptic seizures in the entorhinal cortex. Our findings support the novel concept that synchronization of inhibitory networks is associated with and could be causally linked to seizure initiation.

Footnotes

  • This work was supported by the Italian Health Ministry (Grant Giovani Ricercatori RF 114, Ricerca Corrente) and by Telethon (Grants GGP07278 and GGP 12265).

  • The authors declare no competing financial interests.

  • Correspondence should be addressed to Marco de Curtis, Unit of Epileptology and Experimental Neurophysiology, Fondazione Istituto Neurologico, 20133 Milano, Italy. decurtis{at}istituto-besta.it

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Journal of Neuroscience
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18 Feb 2015
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Synchronous Inhibitory Potentials Precede Seizure-Like Events in Acute Models of Focal Limbic Seizures
Laura Uva, Gian Luca Breschi, Vadym Gnatkovsky, Stefano Taverna, Marco de Curtis
Journal of Neuroscience 18 February 2015, 35 (7) 3048-3055; DOI: 10.1523/JNEUROSCI.3692-14.2015

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Synchronous Inhibitory Potentials Precede Seizure-Like Events in Acute Models of Focal Limbic Seizures
Laura Uva, Gian Luca Breschi, Vadym Gnatkovsky, Stefano Taverna, Marco de Curtis
Journal of Neuroscience 18 February 2015, 35 (7) 3048-3055; DOI: 10.1523/JNEUROSCI.3692-14.2015
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Keywords

  • acute seizure model
  • entorhinal cortex
  • focal seizures
  • in vitro guinea pig brain
  • interictal spikes
  • pre-ictal spikes

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