Sub region-specific modulation of synchronous neuronal burst firing after a kainic acid insult in organotypic hippocampal cultures
- Christopher A Reid†1, 2Email author,
- Brendan EL Adams†1,
- Damian Myers1, 3,
- Terence J O'Brien3 and
- David A Williams1
© Reid et al; licensee BioMed Central Ltd. 2008
Received: 01 November 2007
Accepted: 02 July 2008
Published: 02 July 2008
Excitotoxicity occurs in a number of pathogenic states including stroke and epilepsy. The adaptations of neuronal circuits in response to such insults may be expected to play an underlying role in pathogenesis. Synchronous neuronal firing can be induced in isolated hippocampal slices and involves all regions of this structure, thereby providing a measure of circuit activity. The effect of an excitotoxic insult (kainic acid, KA) on Mg2+-free-induced synchronized neuronal firing was tested in organotypic hippocampal culture by measuring extracellular field activity in CA1 and CA3.
Within 24 hrs of the insult regional specific changes in neuronal firing patterns were evident as: (i) a dramatic reduction in the ability of CA3 to generate firing; and (ii) a contrasting increase in the frequency and duration of synchronized neuronal firing events in CA1. Two distinct processes underlie the increased propensity of CA1 to generate synchronized burst firing; a lack of ability of the CA3 region to 'pace' CA1 resulting in an increased frequency of synchronized events; and a change in the 'intrinsic' properties limited to the CA1 region, which is responsible for increased event duration. Neuronal quantification using NeuN immunoflurescent staining and stereological confocal microscopy revealed no significant cell loss in hippocampal sub regions, suggesting that changes in the properties of neurons within this region were responsible for the KA-mediated excitability changes.
These results provide novel insight into adaptation of hippocampal circuits following excitotoxic injury. KA-mediated disruption of the interplay between CA3 and CA1 clearly increases the propensity to synchronized firing in CA1.
Excitotoxicity is linked to many disease states, the consequences of which are thought to be critical to the pathogenic process [1–8]. Kainic acid (KA), a glutamate receptor agonist is frequently used to model such insults both in vivo and in vitro [9–16]. Excitotoxicity induced by KA initiates a cascade of events at multiple levels, including neuronal death, transcriptional changes in ion channels and altered synaptic plasticity [3, 4, 10, 12, 15, 17–19]. The ultimate pathogenic outcome of an excitotoxic insult is likely to be reflected in changes in neuronal network activity. Identifying changes in network properties is therefore important to our overall understanding of underlying pathogenesis caused by excitotoxcity.
The hippocampal slice preparation is widely used to investigate the cellular and synaptic mechanisms that underlie synchronized network events. In isolated hippocampal slices, network firing is initiated in the CA3 region and propagates along the output pathway of the Schaffer collaterals to the CA1 region where it synchronizes neuronal firing, although CA1-led bursts have been reported [20–26]. Cells within each sub region of the hippocampus are highly heterogeneous and respond quite distinctly to a KA insult. Changes in the hyperpolarization-activated, cyclic nucleotide-gated channels (HCN) that mediate a mixed cationic conductance (Ih) showcase this well. Heterogeneous changes in subtype and extent of HCN mRNA are evident in in vivo  and in vitro  KA models. These changes occur within 24 hours and are likely to impact on network activity in a regional specific manner. KA-mediated changes are unlikely to be limited to HCN, with transcriptional changes in other proteins and structural changes (eg. synaptic reorganization) also able to impact on measures of hippocampal excitability [5, 28–32]. Furthermore, alteration in network properties in one subregion are known to modulate network activity in connecting regions . Synchronized network firing is an encompassing parameter that integrates these various plastic changes.
In this paper, we investigate the impact of KA-mediated excitotoxicity on synchronized network firing in an in vitro model. Within 24 hours following a KA insult the hippocampal slice cultures were essentially unable to generate synchronized neuronal firing in CA3 but recovered this ability by 7 days. Simultaneously, slice cultures showed an increase in synchronized burst firing in CA1 consistent with a hyperexcitable phenotype. This excitability persisted over time. Two distinct mechanisms drive different aspects of the increased propensity to synchronized burst firing in CA1, namely a loss of the 'extrinsic' modulation by the CA3 affects burst timing, and an 'intrinsic' change limited to the CA1 sub region affects burst duration.
Organotypic hippocampal slice cultures exhibit synchronous bursts led by CA3
Kainic acid (KA) treatment dampens CA3 burst firing but increases CA1 excitability
Significant cell death does not account for a loss of CA3 burst firing at the 24 hour time-point following KA treatment
Increased CA1 excitability follows KA treatment
Separation of CA3 increases the rate of occurrence of burst firing in the CA1 region without changing burst duration
Increases in burst duration in the CA1 region following KA insult are maintained in segregated slices
The impact of CA3 segregation on CA1 region excitability was also investigated in slices treated with KA. The IBI of the separated CA1 region did not change (2.05 ± 0.49 s, n = 6) from that measured in intact KA-treated slices (2.32 ± 0.21 s, n = 6. p = 0.63, Fig. 5C). Comparison of this with the reduction in IBI in the CA1 region following separation of untreated slices (1.64 ± 0.19 s, n = 6, p < 0.005), suggests that the reduced IBI of burst events following KA insult is most likely due to a reduction in pacing from the CA3 region.
In untreated cultures, CA1 burst duration tended to decrease when the CA3 was separated from the slice while in KA-treated cultures the duration of the bursts increased. Intriguingly, in KA-treated slices where the CA3 was segregated, the increase in CA1 burst duration was maintained (1.03 ± 0.17 s vs. 1.19 ± 0.17 s, n = 6, Fig. 5D). Therefore, increases in the burst duration post-KA treatment cannot be explained by removal of CA3 input. These results suggest that KA treatment alters the properties of neuronal firing within either the CA1 and/or DG regions of the hippocampal slice to increase burst duration.
DG segregation does not alter CA1 firing
The ability of the DG to display synchronized firing in Mg2+-free ACSF has been reported . The significant reciprocal projections present in hippocampal slice cultures between CA1 and DG raise the possibility that changes in the intrinsic properties of the DG may modulate changes in CA1 burst duration . To establish the relationship between CA1 and DG we recorded from both regions in CA3-deafferented slices. CA1 firing preceded the DG by an average of 15.25 ± 2.34 ms (n = 6), indicating that in the absence of the CA3 region, CA1 paces synchronized firing. However, it remains possible that a reciprocal interplay between CA1 and DG could influence burst duration in CA1 region.
Increases in CA1 region burst duration, but not rate of occurrence, are sustained for up to 7 days following KA insult
To confirm the importance on CA3 input in pacing burst frequency we again separated the CA3 from the CA1 just prior to recording at this later time-point. Following deafferentation we found IBI increased in both control to (2.16 ± 0.08 s to 3.06 ± 0.29 s, p = 0.04, n = 8, Fig. 7C) and KA-treated slices (2.29 ± 0.25 s to 3.41 ± 0.11 s, p = 0.03, n = 8, Fig. 7C). Thus removal of CA3 input again resulted in a disruption in the timing of IBI. However, rather than the decrease seen early after KA insult, we now measured a significant increase in IBI over the intact slices. There remained no significant difference in IBI between treated and control slices (p = 0.63, n = 8, Fig. 7D). Conversely, removal of CA3 input had no significant impact on the burst duration in CA1 of deafferented slices compared to their intact counterparts in control (0.86 ± 0.07 s vs 0.73 ± 0.08, p = 0.08, n = 8, Fig. 7D) or treated slices (1.21 ± 0.11 s vs 1.08 ± 0.12 s, p = 0.11 n = 8, Fig. 7D). The elevated burst duration following KA treatment was maintained regardless of CA3 deafferentation (0.86 ± 0.07 vs 1.21 ± 0.11 s, p = 0.03, n = 8, Fig. 7D).
Here we describe three primary findings. Firstly, that a loss of CA3 pacing 'control' of CA1 can increase excitability in this region. Although not an entirely new concept , this is the first demonstration of such interplay between CA3 and CA1 under pathological conditions. Secondly, that a chemical (KA) rather than a surgical insult is capable of 'isolating' the CA1 region from CA3. Given that KA models excitotoxcity this result provide evidence of a novel hypothesis regarding the mechanisms underlying hippocampal epileptogenesis following an excitotoxic insult that needs further testing in other brain model systems. Finally, that the different aspects of burst behaviour (frequency of events and duration of events) can be modulated by distinct network factors.
Increases in excitability of the CA1 region and hyperexcitable phenotypes
The properties of the CA3 region, including a propensity to bursting and abundant recurrent collaterals, make it an obvious choice for driving a hyperexcitable hippocampus [43–45]. However, hyperexcitability limited to the CA1 region is recognized [16, 32, 46]. An increase in CA1 pyramidal neuron axon sprouting occurs in KA- and pilocarpine-treated animals [5, 28, 29]. De novo recurrent excitatory connections established within the CA1 following an excitotoxic insult are postulated to contribute to a hyperexcitable hippocampus . In this sense the organotypic culture models a hippocampus that has already formed these recurrent CA1 connections. The KA insult therefore may model a further insult under such hyperexcitable conditions, as may be expected in epilepsy cases of multiple and progressively worsening seizures. The sustained changes in burst duration we observe in this model could therefore contribute to overall hippocampal hyperexcitability. Determining the molecular and/or structural basis of a sustained increase in burst duration is therefore important.
Structurally, KA-treated organotypic slices have a greater extent of CA1 pyramidal neuron axon sprouting, a feature that could change the dynamics of synchronization . However, increases in axon sprouting occur on relatively slow time scales, and as such, are unlikely to be responsible for changes noted at the 24 hour time-point. While we observe no cell death in our cultures, selective CA1 interneurons are particularly sensitive to the toxic effects of KA, potentially altering the excitation/inhibition balance to render the CA1 hyperexcitable [16, 47, 48]. CA1 pyramidal neurons make recurrent excitatory contacts with interneurons producing feedback inhibition, and a specific loss of this function, through either loss of interneurons or changes in the intrinsic properties of interneurons may prolong burst duration [48, 49]. Burst appear to be terminated by activity-dependent depression at recurrent excitatory synapses, and IBI is predicted to be primarily due to the period of recovery from synaptic depression [50–52]. However, an alternative proposition for the pacing of IBIs is the slow build-up of excitation governed by Ih [20, 53, 54]. As already noted, transcriptional changes in ion channel expression do occur on short time frames and could contribute to changes seen. Two good candidates are alterations in Ih and T-type Ca2+ channels. Increased CA1 neuronal bursting due to the de novo expression of Ni2+-sensitive T-type Ca2+ channels is associated with epilepsy in the pilocarpine model of temporal lobe epilepsy (TLE) [55, 56]. Similarly, increased HCN channel function in CA1 pyramidal neurons of the febrile convulsive model of TLE is predicted to enhance synchronized neuronal firing .
What causes a transient decrease in CA3 excitability?
The basis of the transient absence of Mg2+-free synchronized firing in the CA3 region remains to be determined. KA applied for longer periods to organotypic hippocampal slices do illicit a selective degeneration of CA3 pyramidal cells [10, 57], raising the possibility that rapid cell death may be responsible. However, KA insult had no effect on the count of pyramidal neurons, or stratum lucidium and stratum radiatum inhibitory interneurons at either the 24 hour or 7 day time-points in our study. This is consistent with previous studies that suggest that long-term, (12 to 48 hours) rather than short-term, (4 to 6 hours) KA exposure results in cell death in organotypic cultures at similar concentrations [7, 9, 10, 12]. Furthermore, a return of CA3 bursting activity occurs at 7 days suggesting that neurons required to develop synchronized firing are present at the 24 hour time-point, but are unable to do so. Therefore, the acute reduction in burst activity is more likely to reflect a functional change in CA3 sub-region neurons rather than be a consequence of cell death (or cells in the process of dying). Previous studies of acute KA application have identified a wide range of hippocampal alterations, including changes in GABAA and GABAB receptor expression, matrix metalloproteinase activity, mossy fiber innervation, and expression of neuronal and glial glutamate transporters and ongoing neuronal degeneration [9, 12, 18, 58–60] or transcriptional changes as previously discussed [3, 4, 56, 61–63]. Interneurons play an essential role in neuronal network synchronization and disruption of their input is expected to alter CA3 burst activity . Loss of GABAB receptor-mediated heterosynaptic depression in mossy fibres innervating the CA3, postulated to contribute to maintenance of seizure activity, has also been reported 24 hours after pilocarpine exposure . Therefore changes to the intrinsic properties of excitatory or inhibitory neurons may contribute to the loss of activity in CA3.
Potential pathophysiological implications
In rats in vivo, KA-induced status epilepticus and its sequelae are widely used to model the development of TLE . In vitro, application of KA to organotypic slices results in many of the hallmarks of TLE, including mossy fiber sprouting, eventual hippocampal neuronal death (particularly in the CA3, dentate hilus and CA1 regions), and an enhanced propensity to synchronized neuronal firing [9, 10, 57]. Our results suggest that in the hippocampus, KA-mediated excitotoxic stimuli cause changes in neuronal network firing patterns that are highly region-specific. Paradoxically, reduced excitability in the CA3 region can enhance excitability in the CA1 region. Conceptually, this provides a novel means by which hippocampal excitability can be increased. In this scheme an adaptive process, presumably attempting to limit hyperexcitability in the CA3, engages or affects a mechanism resulting in an increased CA1 excitability. A similar mechanism has been proposed to unmask recurrent entorhinal seizures in intact hippocampal-entorhinal slices in which the Shaffer collateral fibers had been cut [33, 43]. A potential implication of this finding relates to the progressive neuronal death in selected hippocampal subfields including CA3 noted in patients and most models of TLE. This takes on extra significance given that an increase in CA1 pyramidal neuron axon sprouting occurs in KA- and pilocarpine-treated animals [5, 28, 29]. A combination of these factors and 'intrinsic' changes responsible for burst duration in CA1 may contribute to a progressively worsening of seizures noted in TLE.
Excitotoxicity is one of the major pathological processes underlying both acute and chronic neurological diseases, including stroke and epilepsy. Here we describe the impact on regional neuronal firing patterns in CA1 and CA3 of an acute KA-induced excitotoxic insult to hippocampal organotypic cultures. A KA insult resulted in a significant dampening of the capacity of CA3 regions to generate Mg2+-free induced burst neuronal firing at the 24 hours time-point. In contrast, this insult lead to increased propensity of the CA1 region to synchronized neuronal burst firing by increasing both the rate of occurrence and duration of the events. A loss of 'pacing' by CA3 of the synchronisation of CA1 accounted for the increased rate of occurrence in bursting events. Changes in the properties limited to the CA1 region were responsible for increased event duration. These findings provide a framework on which to consider potential contributors to hippocampal hyperexcitability in TLE.
All procedures undertaken in this project were ratified by the University of Melbourne animal ethics committee. Transverse 300 μm slices of hippocampus were cut from 7 to 9-day-old Sprague Dawley rat pups and cultured according to published methods  on Millicell CM membranes (Millipore MA, USA) for 7–14 days prior to use, as described previously . A subset of cultures was treated with 6 μM KA (Sigma MI, USA) for 8 hours and returned to normal medium for incubation prior to examination the following day, within 24 hours post insult. Several slices are analyzed during one day therefore the time after insult varies from approximately 16 hours to 24 hours, herein referred to this as the 24 hour time point. Physical separation of CA3/dentate gyrus (DG) regions was achieved by using a scalpel blade under a binocular dissecting microscope. All surgical interventions were made just prior to electrophysiological recordings. The selectivity of this separation procedure is highlighted [see Additional file 1].
Extracellular field potential recordings
Slices and their supporting membranes were transferred to a recording bath where they were continually superfused with oxygenated (95%O2/5%CO2) artificial cerebrospinal fluid (ACSF) maintained at 30°–32°C with a TC-324B temperature controller (Warner Instruments, Hamden, CT). A subset of cultures recorded at room temperature yielded less robust rhythmic firing so a bath temperature of 30–32°C was used. Except where noted the ACSF contained (in mM): 120 NaCl, 3 KCl, 1 MgCl2, 2 CaCl2, 1.2 NaHPO4, 23 NaHCO3, 11 glucose. Slices were viewed through an Olympus BX51WI microscope using a XL Fluor 4X/340 NA 0.28 objective (Olympus, Japan). Simultaneous recordings from the CA3 and CA1 regions were acquired with a MiniDigi 1A two-channel acquisition system (Axon Instruments, CA, USA) using custom-made bipolar 0.025 mm polyimide insulated tungsten (Goodfellow, UK) wire electrodes, through an A-M Systems 3000 AC/DC amplifier (A-M Systems, WA, USA), Gain = 1 K, High Pass = 1 Hz, Low pass = 0.1 kHz, and recorded in AxoScope9 software (Axon Instruments, CA, USA) while sampling at 500 Hz. Recordings electrodes were alternated between region for each successive experiment ensure that differences in timing were not due to electronic delay. Mg2+-free ACSF perfusate, identical in composition to ACSF except for equimolar CaCl2 substitution for MgCl2, was used to promote synchronous firing, presumably by removal of NMDA receptor block, as previously described [34–36].
Neurons were specifically labeled for cell counting with neuronal nuclear antigen (NeuN) antibody. Cultures were washed in phosphate-buffered saline (PBS) 0.1 M, pH 7.4 and treated with blocking buffer (BB) containing 10% foetal calf serum + 1% Triton X-100 for 30 min. Cultures were incubated overnight at 4°C with mouse anti-NeuN (Chemicon International, MAB 377, USA) at 1:1000 in BB, washed and incubated with secondary Alexa 594 donkey anti-mouse antibody (Molecular Probes) for 2 hours. Images were captured on an Olympus FV1000 confocal laser scanning microscope with spectral analysis using a UPLANSApo 20x/0.75 objective lens, running Olympus FV10 ASW Ver 1.6a image acquisition software with 3D analysis (Olympus Australia Pty Ltd). Post-hoc cell density analysis was performed using Image Pro Plus, Ver 6.2 (QImaging, Surrey, BC, Canada).
Electrophysiological parameter measurements and statistical analysis
Inter-burst interval (IBI) was defined as the interval between the negative peaks of two adjacent events, or when bursts occurred in clusters, the interval between the first events in two consecutive clusters [see Additional file 2] . Measurement of IBI were normalized between recordings and slices to start 2 minutes after bursting had established a rhythmic firing pattern and continued for a minimum of 30 bursts. Burst duration was defined as the time from the negative peaks of the first and last spikes in a burst. The frequency of spikes within a burst was determined by counting the number of spikes occurring during this time. Regularity of the occurrence of synchronized events was measured by the coefficient of variance of IBI (cVIBI), calculated as cV= SD/mean, determined within each recording and averaged per group. The cVIBI was also used to monitor the consistency of recordings to help ensure data was normalized between slices. Data is presented as mean ± standard error of the mean (SEM). A chi-squared test was performed to test proportion of slices oscillating (Fig. 2C). Differences between two means were tested by a two-tailed student's t-test (Figs. 3, 4 and 7). One-way ANOVA was used where more than two means were compared (Figs. 5 and 6). Significance level was set at p < 0.05. Slices with no evidence of burst firing were excluded from the analysis. For figures, bars represent mean ± SEM, *, P < 0.05.
We wish to thank Didier Pinault for critical feedback on this manuscript. CAR, DAW and TOB independently acknowledge the support of NHMRC funding from the Australian Government. DAW and CAR acknowledge the support of ARC funding from the Australian Government. CAR would like to also acknowledge the support of a RD Wright Fellowship awarded by the University of Melbourne. BELA was supported on an MRS PhD studentship.
- Bengzon J, Mohapel P, Ekdahl CT, Lindvall O: Neuronal apoptosis after brief and prolonged seizures. Prog Brain Res. 2002, 135: 111-119.PubMedGoogle Scholar
- Bergold PJ, Casaccia-Bonnefil P, Zeng XL, Federoff HJ: Transsynaptic neuronal loss induced in hippocampal slice cultures by a herpes simplex virus vector expressing the GluR6 subunit of the kainate receptor. Proc Natl Acad Sci U S A. 1993, 90 (13): 6165-6169.PubMed CentralPubMedGoogle Scholar
- Brewster A, Bender RA, Chen Y, Dube C, Eghbal-Ahmadi M, Baram TZ: Developmental febrile seizures modulate hippocampal gene expression of hyperpolarization-activated channels in an isoform- and cell-specific manner. J Neurosci. 2002, 22 (11): 4591-4599.PubMed CentralPubMedGoogle Scholar
- Chen K, Aradi I, Thon N, Eghbal-Ahmadi M, Baram TZ, Soltesz I: Persistently modified h-channels after complex febrile seizures convert the seizure-induced enhancement of inhibition to hyperexcitability. Nat Med. 2001, 7 (3): 331-337.PubMed CentralPubMedGoogle Scholar
- Esclapez M, Hirsch JC, Ben-Ari Y, Bernard C: Newly formed excitatory pathways provide a substrate for hyperexcitability in experimental temporal lobe epilepsy. J Comp Neurol. 1999, 408 (4): 449-460.PubMedGoogle Scholar
- Fujikawa DG, Shinmei SS, Cai B: Kainic acid-induced seizures produce necrotic, not apoptotic, neurons with internucleosomal DNA cleavage: implications for programmed cell death mechanisms. Neuroscience. 2000, 98 (1): 41-53.PubMedGoogle Scholar
- Kristensen BW, Noraberg J, Zimmer J: Comparison of excitotoxic profiles of ATPA, AMPA, KA and NMDA in organotypic hippocampal slice cultures. Brain Res. 2001, 917 (1): 21-44.PubMedGoogle Scholar
- Nadler JV, Cuthbertson GJ: Kainic acid neurotoxicity toward hippocampal formation: dependence on specific excitatory pathways. Brain Res. 1980, 195 (1): 47-56.PubMedGoogle Scholar
- Gatherer M, Sundstrom LE: Mossy fibre innervation is not required for the development of kainic acid toxicity in organotypic hippocampal slice cultures. Neurosci Lett. 1998, 253 (2): 119-122.PubMedGoogle Scholar
- Routbort MJ, Bausch SB, McNamara JO: Seizures, cell death, and mossy fiber sprouting in kainic acid-treated organotypic hippocampal cultures. Neuroscience. 1999, 94 (3): 755-765.PubMedGoogle Scholar
- Bausch SB, McNamara JO: Contributions of mossy fiber and CA1 pyramidal cell sprouting to dentate granule cell hyperexcitability in kainic acid-treated hippocampal slice cultures. J Neurophysiol. 2004, 92 (6): 3582-3595.PubMedGoogle Scholar
- Holopainen IE, Jarvela J, Lopez-Picon FR, Pelliniemi LJ, Kukko-Lukjanov TK: Mechanisms of kainate-induced region-specific neuronal death in immature organotypic hippocampal slice cultures. Neurochem Int. 2004, 45 (1): 1-10.PubMedGoogle Scholar
- Shah MM, Anderson AE, Leung V, Lin X, Johnston D: Seizure-induced plasticity of h channels in entorhinal cortical layer III pyramidal neurons. Neuron. 2004, 44 (3): 495-508.PubMed CentralPubMedGoogle Scholar
- Pollard H, Charriaut-Marlangue C, Cantagrel S, Represa A, Robain O, Moreau J, Ben-Ari Y: Kainate-induced apoptotic cell death in hippocampal neurons. Neuroscience. 1994, 63 (1): 7-18.PubMedGoogle Scholar
- Lauren HB, Lopez-Picon FR, Korpi ER, Holopainen IE: Kainic acid-induced status epilepticus alters GABA receptor subunit mRNA and protein expression in the developing rat hippocampus. J Neurochem. 2005, 94 (5): 1384-1394.PubMedGoogle Scholar
- Sanon N, Carmant L, Emond M, Congar P, Lacaille JC: Short-term effects of kainic acid on CA1 hippocampal interneurons differentially vulnerable to excitotoxicity. Epilepsia. 2005, 46 (6): 837-848.PubMedGoogle Scholar
- Furtinger S, Bettler B, Sperk G: Altered expression of GABAB receptors in the hippocampus after kainic-acid-induced seizures in rats. Brain Res Mol Brain Res. 2003, 113 (1-2): 107-115.PubMedGoogle Scholar
- Jourquin J, Tremblay E, Decanis N, Charton G, Hanessian S, Chollet AM, Le Diguardher T, Khrestchatisky M, Rivera S: Neuronal activity-dependent increase of net matrix metalloproteinase activity is associated with MMP-9 neurotoxicity after kainate. Eur J Neurosci. 2003, 18 (6): 1507-1517.PubMedGoogle Scholar
- Jung S, Jones TD, Lugo JN, Sheerin AH, Miller JW, D'Ambrosio R, Anderson AE, Poolos NP: Progressive Dendritic HCN Channelopathy during Epileptogenesis in the Rat Pilocarpine Model of Epilepsy. J Neurosci. 2007, 27 (47): 13012-13021.PubMed CentralPubMedGoogle Scholar
- Agmon A, Wells JE: The role of the hyperpolarization-activated cationic current I(h) in the timing of interictal bursts in the neonatal hippocampus. J Neurosci. 2003, 23 (9): 3658-3668.PubMedGoogle Scholar
- Cobb SR, Bulters DO, Suchak S, Riedel G, Morris RG, Davies CH: Activation of nicotinic acetylcholine receptors patterns network activity in the rodent hippocampus. J Physiol. 1999, 518 ( Pt 1): 131-140.Google Scholar
- Cobb SR, Larkman PM, Bulters DO, Oliver L, Gill CH, Davies CH: Activation of Ih is necessary for patterning of mGluR and mAChR induced network activity in the hippocampal CA3 region. Neuropharmacology. 2003, 44 (3): 293-303.PubMedGoogle Scholar
- Fisahn A, Pike FG, Buhl EH, Paulsen O: Cholinergic induction of network oscillations at 40 Hz in the hippocampus in vitro. Nature. 1998, 394 (6689): 186-189.PubMedGoogle Scholar
- Gutierrez R, Armand V, Schuchmann S, Heinemann U: Epileptiform activity induced by low Mg2+ in cultured rat hippocampal slices. Brain Res. 1999, 815 (2): 294-303.PubMedGoogle Scholar
- Williams JH, Kauer JA: Properties of carbachol-induced oscillatory activity in rat hippocampus. J Neurophysiol. 1997, 78 (5): 2631-2640.PubMedGoogle Scholar
- Lewis DV, Jones LS, Mott DD: Hippocampal epileptiform activity induced by magnesium-free medium: differences between areas CA1 and CA2-3. Epilepsy Res. 1990, 6 (2): 95-101.PubMedGoogle Scholar
- Richichi C, Brewster AL, Bender RA, Simeone TA, Zha Q, Yin HZ, Weiss JH, Baram TZ: Mechanisms of seizure-induced 'transcriptional channelopathy' of hyperpolarization-activated cyclic nucleotide gated (HCN) channels. Neurobiol Dis. 2008, 29 (2): 297-305.PubMed CentralPubMedGoogle Scholar
- Perez Y, Morin F, Beaulieu C, Lacaille JC: Axonal sprouting of CA1 pyramidal cells in hyperexcitable hippocampal slices of kainate-treated rats. Eur J Neurosci. 1996, 8 (4): 736-748.PubMedGoogle Scholar
- Smith BN, Dudek FE: Network interactions mediated by new excitatory connections between CA1 pyramidal cells in rats with kainate-induced epilepsy. J Neurophysiol. 2002, 87 (3): 1655-1658.PubMedGoogle Scholar
- Meier CL, Dudek FE: Spontaneous and stimulation-induced synchronized burst afterdischarges in the isolated CA1 of kainate-treated rats. J Neurophysiol. 1996, 76 (4): 2231-2239.PubMedGoogle Scholar
- Meier CL, Obenaus A, Dudek FE: Persistent hyperexcitability in isolated hippocampal CA1 of kainate-lesioned rats. J Neurophysiol. 1992, 68 (6): 2120-2127.PubMedGoogle Scholar
- Williams S, Vachon P, Lacaille JC: Monosynaptic GABA-mediated inhibitory postsynaptic potentials in CA1 pyramidal cells of hyperexcitable hippocampal slices from kainic acid-treated rats. Neuroscience. 1993, 52 (3): 541-554.PubMedGoogle Scholar
- Barbarosie M, Louvel J, Kurcewicz I, Avoli M: CA3-Released entorhinal seizures disclose dentate gyrus epileptogenicity and unmask a temporoammonic pathway. J Neurophysiol. 2000, 83 (3): 1115-1124.PubMedGoogle Scholar
- Collingridge GL, Herron CE, Lester RA: Synaptic activation of N-methyl-D-aspartate receptors in the Schaffer collateral-commissural pathway of rat hippocampus. J Physiol. 1988, 399: 283-300.PubMed CentralPubMedGoogle Scholar
- Mody I, Lambert JD, Heinemann U: Low extracellular magnesium induces epileptiform activity and spreading depression in rat hippocampal slices. J Neurophysiol. 1987, 57 (3): 869-888.PubMedGoogle Scholar
- Stanton PK, Jones RS, Mody I, Heinemann U: Epileptiform activity induced by lowering extracellular [Mg2+] in combined hippocampal-entorhinal cortex slices: modulation by receptors for norepinephrine and N-methyl-D-aspartate. Epilepsy Res. 1987, 1 (1): 53-62.PubMedGoogle Scholar
- Walther H, Lambert JD, Jones RS, Heinemann U, Hamon B: Epileptiform activity in combined slices of the hippocampus, subiculum and entorhinal cortex during perfusion with low magnesium medium. Neurosci Lett. 1986, 69 (2): 156-161.PubMedGoogle Scholar
- Borck C, Jefferys JG: Seizure-like events in disinhibited ventral slices of adult rat hippocampus. J Neurophysiol. 1999, 82 (5): 2130-2142.PubMedGoogle Scholar
- Ishizuka N, Cowan WM, Amaral DG: A quantitative analysis of the dendritic organization of pyramidal cells in the rat hippocampus. J Comp Neurol. 1995, 362 (1): 17-45.PubMedGoogle Scholar
- Williams S, Samulack DD, Beaulieu C, LaCaille JC: Membrane properties and synaptic responses of interneurons located near the stratum lacunosum-moleculare/radiatum border of area CA1 in whole-cell recordings from rat hippocampal slices. J Neurophysiol. 1994, 71 (6): 2217-2235.PubMedGoogle Scholar
- Andersen P: Inhibitory circuits in the thalamus and hippocampus--an appraisal after 40 years. Prog Neurobiol. 2006, 78 (3-5): 264-271.PubMedGoogle Scholar
- Andersen P: The hippocampus book. 2007, Oxford ; New York , Oxford University Press, xx, 832 p..Google Scholar
- Barbarosie M, Avoli M: CA3-driven hippocampal-entorhinal loop controls rather than sustains in vitro limbic seizures. J Neurosci. 1997, 17 (23): 9308-9314.PubMedGoogle Scholar
- Bausch SB, McNamara JO: Synaptic connections from multiple subfields contribute to granule cell hyperexcitability in hippocampal slice cultures. J Neurophysiol. 2000, 84 (6): 2918-2932.PubMedGoogle Scholar
- Mohajerani MH, Cherubini E: Spontaneous recurrent network activity in organotypic rat hippocampal slices. Eur J Neurosci. 2005, 22 (1): 107-118.PubMedGoogle Scholar
- Reid CA, Coleman HA, Finkelstein DI, Horne MK, Drago J: Null mutation of the alpha4 nicotinic receptor subunit increases the propensity of muscarinic-mediated neuronal bursting in mouse hippocampal slices. Neuropharmacology. 2006, 51 (3): 587-596.PubMedGoogle Scholar
- Oliva AA, Lam TT, Swann JW: Distally directed dendrotoxicity induced by kainic Acid in hippocampal interneurons of green fluorescent protein-expressing transgenic mice. J Neurosci. 2002, 22 (18): 8052-8062.PubMedGoogle Scholar
- Mann EO, Paulsen O: Role of GABAergic inhibition in hippocampal network oscillations. Trends Neurosci. 2007, 30 (7): 343-349.PubMedGoogle Scholar
- Morin F, Beaulieu C, Lacaille JC: Cell-specific alterations in synaptic properties of hippocampal CA1 interneurons after kainate treatment. J Neurophysiol. 1998, 80 (6): 2836-2847.PubMedGoogle Scholar
- Lebovitz RM: Autorhythmicity of spontaneous interictal spike discharge at hippocampal penicillin foci. Brain Res. 1979, 172 (1): 35-55.PubMedGoogle Scholar
- Staley KJ, Bains JS, Yee A, Hellier J, Longacher JM: Statistical model relating CA3 burst probability to recovery from burst-induced depression at recurrent collateral synapses. J Neurophysiol. 2001, 86 (6): 2736-2747.PubMedGoogle Scholar
- Staley KJ, Longacher M, Bains JS, Yee A: Presynaptic modulation of CA3 network activity. Nat Neurosci. 1998, 1 (3): 201-209.PubMedGoogle Scholar
- Luthi A, Bal T, McCormick DA: Periodicity of thalamic spindle waves is abolished by ZD7288,a blocker of Ih. J Neurophysiol. 1998, 79 (6): 3284-3289.PubMedGoogle Scholar
- Soltesz I, Lightowler S, Leresche N, Jassik-Gerschenfeld D, Pollard CE, Crunelli V: Two inward currents and the transformation of low-frequency oscillations of rat and cat thalamocortical cells. J Physiol. 1991, 441: 175-197.PubMed CentralPubMedGoogle Scholar
- Sanabria ER, Su H, Yaari Y: Initiation of network bursts by Ca2+-dependent intrinsic bursting in the rat pilocarpine model of temporal lobe epilepsy. J Physiol. 2001, 532 (Pt 1): 205-216.PubMed CentralPubMedGoogle Scholar
- Pitkanen A, Sutula TP: Is epilepsy a progressive disorder? Prospects for new therapeutic approaches in temporal-lobe epilepsy. Lancet Neurol. 2002, 1 (3): 173-181.PubMedGoogle Scholar
- Silva AP, Pinheiro PS, Carvalho AP, Carvalho CM, Jakobsen B, Zimmer J, Malva JO: Activation of neuropeptide Y receptors is neuroprotective against excitotoxicity in organotypic hippocampal slice cultures. Faseb J. 2003, 17 (9): 1118-1120.PubMedGoogle Scholar
- Holopainen IE, Lauren HB: Neuronal activity regulates GABAA receptor subunit expression in organotypic hippocampal slice cultures. Neuroscience. 2003, 118 (4): 967-974.PubMedGoogle Scholar
- Montpied P, de Bock F, Lerner-Natoli M, Bockaert J, Rondouin G: Hippocampal alterations of apolipoprotein E and D mRNA levels in vivo and in vitro following kainate excitotoxicity. Epilepsy Res. 1999, 35 (2): 135-146.PubMedGoogle Scholar
- Simantov R, Crispino M, Hoe W, Broutman G, Tocco G, Rothstein JD, Baudry M: Changes in expression of neuronal and glial glutamate transporters in rat hippocampus following kainate-induced seizure activity. Brain Res Mol Brain Res. 1999, 65 (1): 112-123.PubMedGoogle Scholar
- Bender RA, Soleymani SV, Brewster AL, Nguyen ST, Beck H, Mathern GW, Baram TZ: Enhanced expression of a specific hyperpolarization-activated cyclic nucleotide-gated cation channel (HCN) in surviving dentate gyrus granule cells of human and experimental epileptic hippocampus. J Neurosci. 2003, 23 (17): 6826-6836.PubMed CentralPubMedGoogle Scholar
- Magee JC, Carruth M: Dendritic voltage-gated ion channels regulate the action potential firing mode of hippocampal CA1 pyramidal neurons. J Neurophysiol. 1999, 82 (4): 1895-1901.PubMedGoogle Scholar
- Mody I, Heinemann U: NMDA receptors of dentate gyrus granule cells participate in synaptic transmission following kindling. Nature. 1987, 326 (6114): 701-704.PubMedGoogle Scholar
- Chandler KE, Princivalle AP, Fabian-Fine R, Bowery NG, Kullmann DM, Walker MC: Plasticity of GABA(B) receptor-mediated heterosynaptic interactions at mossy fibers after status epilepticus. J Neurosci. 2003, 23 (36): 11382-11391.PubMedGoogle Scholar
- Morimoto K, Fahnestock M, Racine RJ: Kindling and status epilepticus models of epilepsy: rewiring the brain. Prog Neurobiol. 2004, 73: 1-60.PubMedGoogle Scholar
- Stoppini L, Buchs PA, Muller D: A simple method for organotypic cultures of nervous tissue. J Neurosci Methods. 1991, 37 (2): 173-182.PubMedGoogle Scholar
- Reid CA, Fabian-Fine R, Fine A: Postsynaptic calcium transients evoked by activation of individual hippocampal mossy fiber synapses. J Neurosci. 2001, 21 (7): 2206-2214.PubMedGoogle Scholar
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