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Experimental prolonged febrile seizures (FS) lead to structural and molecular changes that promote hippocampal hyperexcitability and reduce seizure threshold to further convulsants. However, whether these seizures provoke later-onset epilepsy, as has been suspected in humans, has remained unclear. Previously, intermittent EEGs with behavioural observations for motor seizures failed to demonstrate spontaneous seizures in adult rats subjected to experimental prolonged FS during infancy. Because limbic seizures may be behaviourally subtle, here we determined the presence of spontaneous limbic seizures using chronic video monitoring with concurrent hippocampal and cortical EEGs, in adult rats (starting around 3 months of age) that had sustained experimental FS on postnatal day 10. These subjects were compared with groups that had undergone hyperthermia but in whom seizures had been prevented (hyperthermic controls), as well as with normothermic controls. Only events that fulfilled both EEG and behavioural criteria, i.e. electro-clinical events, were considered spontaneous seizures. EEGs (over 400 recorded hours) were normal in all normothermic and hyperthermic control rats, and none of these animals developed spontaneous seizures. In contrast, prolonged early-life FS evoked spontaneous electro-clinical seizures in 6 out of 17 experimental rats (35.2%). These seizures consisted of sudden freezing (altered consciousness) and typical limbic automatisms that were coupled with polyspike/sharp-wave trains with increasing amplitude and slowing frequency on EEG. In addition, interictal epileptiform discharges were recorded in 15 (88.2%) of the experimental FS group and in none of the controls. The large majority of hippocampally-recorded seizures were heralded by diminished amplitude of cortical EEG, that commenced half a minute prior to the hippocampal ictus and persisted after seizure termination. This suggests a substantial perturbation of normal cortical neuronal activity by these limbic spontaneous seizures. In summary, prolonged experimental FS lead to later-onset limbic (temporal lobe) epilepsy in a significant proportion of rats, and to interictal epileptifom EEG abnormalities in most others, and thus represent a model that may be useful to study the relationship between FS and human temporal lobe epilepsy.
Experimental prolonged febrile seizures (FS) can be evoked in infant rats at the age where hippocampal development is equivalent to that of human infants (Avishai-Eliner et al., 2002). These seizures: (i) are limbic in semiology and involve the hippocampal formation (Dubé et al., 2000); (ii) induce transient neuronal injury but no cell death (Toth et al., 1998; Bender et al., 2003a); (iii) lead to altered MRI T2-signal in several limbic areas (Dubé et al., 2004); (iv) cause profound and enduring alterations in the expression of several channel genes (Brewster et al., 2002, 2005); and, (v) enhance hippocampal excitability long-term (Dubé et al., 2000).
However, whether these prolonged (~20 min) experimental FS result in epilepsy, as has been suspected for the human condition (Annegers et al., 1987; Hesdorffer and Hauser, 2002), has remained unclear. In the human, retrospective analyses have implicated early-life FS as a risk factor for the development of limbic, temporal lobe epilepsy (TLE; Cendes et al., 1993; French et al., 1993). However, whether early-life FS actually cause this TLE, or are simply indicative of other, perhaps genetically determined (Fernandez et al., 1998; Wallace et al., 2001) processes that eventually result in TLE, cannot be determined in correlative clinical studies. This question is particularly complex, because prospective studies in children with FS have not demonstrated the eventual development of TLE in the majority of those involved (Shinnar, 1998).
In the experimental model developed by the authors, adult animals that had endured prolonged FS early in life were originally monitored using intermittent, day-time EEG, without concurrent video recording or close behavioural observation. This approach did not demonstrate the development of spontaneous motor seizures after experimental prolonged FS. The lack of detection of epilepsy could be attributable either to a true absence of epileptogenesis after prolonged FS, or to missed spontaneous seizures. In view of the persistent hyperexcitability and the pro-epileptic molecular changes in hippocampi of rats that had sustained FS (see above), we tested the hypothesis that systematic video-EEG monitoring, particularly at night (Quigg et al., 1998) may provide a more sensitive tool for investigating whether spontaneous seizures result from prolonged experimental FS.
Immature Sprague Dawley-derived rats were born and maintained in quiet facilities under controlled temperatures and light schedule with unlimited food and water. Cages were monitored every 12 h for the presence of pups and the date of birth was considered as day 0. On postnatal day (P) 2, litters were culled to 12 pups. When weaned (on P21), rats were housed 2–3 per cage. Experimental procedures were approved by Institutional Animal Care Committees and conformed to NIH guidelines.
Prolonged experimental FS were induced as described (Toth et al., 1998; Dubé et al., 2000). On P10, rat pups (n = 17) were placed in a 3 l jar and their core temperature raised using a regulated stream of heated air to ~41°C (simulating high fever). Core temperatures (shown to correlate closely with brain temperatures; Dubé et al., 2005a) were measured at baseline, seizure onset, and every 2 min during the seizures. This procedure leads to seizures in virtually all rats with a threshold at ~40.8°C (Dubé et al., 2000). Hyperthermic temperatures (40.2–41.5°C) were maintained for 30 min, and total seizure time was ~24 min. The behavioural seizures in this paradigm are stereotyped, consisting of arrest of heat-induced hyperkinesis followed by facial automatisms, often followed by body flexion. These behavioural events correlate with electrographic hippocampal seizures (Toth et al., 1998; Dubé et al., 2000; Brewster et al., 2002; Bender et al., 2003a). Hyperthermic controls (n = 6) were generated by subjecting littermates to the same duration of hyperthermia, but blocking the resulting seizures by treating the rats with the rapidly acting barbiturate pentobarbital (37 mg/kg, i.p) 15 min prior to the induction of hyperthermia. In one of these rats, brief behavioural seizures were observed during the first 2 min of hyperthermia, so it was excluded from analysis. An additional control group included littermates of the experimental group that were removed from the cage (to control for potential stress) and their core temperatures kept within the normal range for age (normothermic controls, n = 8).
Two months after prolonged FS (on postnatal day 81 ± 2), rats were implanted unilaterally with twisted wire bipolar electrodes with 0.5 mm vertical tip separation, into the dorsal hippocampus (using the coordinates AP = −3.7, L = 2.7, V = −3.7 mm with reference to bregma). Cortical electrodes (Plastics One, Roanoke, VA, USA) were positioned ipsilaterally over the frontoparietal cortex, and a ground electrode was placed in the cerebellum. The assembly was anchored with dental cement and four stainless steel screws. Hippocampal and cortical recordings were performed via long flexible cables (Plastics One, Roanoke, VA, USA) in freely moving, non-anaesthetized rats.
Starting one week after surgery, digital video-EEG recordings were carried out chronically, using 5 h sessions at night (from 11 p.m. to 4 a.m.; Quigg et al., 1998). A minimum of five recordings was obtained per rat, on postnatal days 90, 105, 120, 135, 165 and 180 (see Fig. 1). Loss of the recording electrode assembly did not permit an equal number of sessions for each rat, and one animal was recorded over 11 sessions. In total, over 200 h of video-EEG were recorded for each control group (normothermic and hyperthermic) and ~400 h were available for analysis for the prolonged FS group.
Electrophysiological data were recorded at a frequency band of 1–50 Hz, and sampled at 100 Hz/channel (4 channels) using Powerlab 8SP (AD Instruments, Grand Junction, CO, USA) equipped with Chart 4 for Windows. The EEG recordings were synchronized with video monitoring using a commercial video camera (camcorder, ZR40, Canon Inc, Japan).
All analyses were carried out without knowledge of treatment. EEGs were first analysed visually, by browsing the digital records on a computer screen for seizures and for interictal events. Electrographic seizures were defined as follows (modified from Galvan et al., 2000 and Nairismagi et al., 2004): EEG parameters of electrographic seizures included the presence of polyspikes or sharp-waves (amplitude >2-fold background) that lasted >6 s. In addition, the progression of the amplitude and the frequencies of the discharges throughout a given seizure were analysed, because typical seizures are characterized by increasing amplitude and slowing frequency as the seizure progresses.
Interictal events were shorter than 5 s, and were not associated with behavioural change. They also lacked the typical progression of discharge frequency and amplitude (see Results). Video-taped behaviour concurrent with EEG changes was analysed. Typical behaviours associated with limbic seizures in humans and rodents, i.e. sudden cessation of activity, head bobbing or ‘jerk’, facial automatisms, prolonged immobility with staring, and alternating or bilateral clonus, were sought during these sequences. The final definition of a seizure required both electrographic and behavioural correlates, i.e. only electro-clinical events were considered seizures for the purpose of analysis.
For further analysis, data were exported from Chart 4 for Windows to Wave format and processed using MATLAB. The raw energy spectra of individual rat EEGs were calculated using fast Fourier transform. Each EEG recording was segmented into consecutive one second windows with 0.5 s overlap. Sequences containing severe movement artefacts were identified and excluded from analysis.
At the conclusion of the video-EEG monitoring, rats were sacrificed, brains were rapidly removed and frozen on dry ice. For histological analysis, coronal serial sections (20 μm) were cut throughout the entire hippocampus using a cryostat. Neuronal counts were performed on every 25th section of a hippocampal series (yielding 9–10 sections from septal to caudal poles). These sections were stained with 1% cresyl violet and examined for electrode placement, then used for neuronal counts in hilus and CA1 of the dorsal hippocampus contralateral to the implantation site. Counts (under ×400 magnification) were performed using stereological principles (Gundersen and Jensen, 1987), by an investigator unaware of the experimental group-status of the sections. Areas for analysis were defined as follows (Fig. 8A): the hilus was defined by its borders with the granule cell layer and by straight lines connecting the tips of the granule cell layer with the proximal end of CA3 pyramidal layer (Buckmaster and Dudek, 1997). In CA1, neuronal numbers were analysed in two, 250 μm wide vertical columns, the first positioned above the midpoint of the suprapyramidal blade of the granule cell layer and the second at its tip. Neurons were included when their nucleus was clearly identifiable and was located >50% within the selected area. Abercrombie's correction (Abercrombie, 1946) was applied and neuronal densities (neurons/mm3) were then determined by dividing the extrapolated number of neurons (counts ×25) by the volume calculated according to Cavalieri's principle (Gundersen and Jensen, 1987).
Prolonged FS experiencing animals were compared with age-matched control groups using ANOVA with post hoc tests or with Student's t-test, paired or not, as appropriate, using Prism software (GraphPad, San Diego, CA, USA). Values are reported as means ± SEM.
EEGs (over 400 recorded hours) were normal in the normothermic and hyperthermic control rats. None of the control animals developed spontaneous seizures throughout the period of monitoring (>3 months). Early-life prolonged FS evoked electro-clinical (i.e. both behavioural and electrographic) spontaneous seizures in 6 of the 17 experimental rats (35.2% of total) and interictal events in 15 (88.2% of the group; Fig. 2).
Electrographic seizures recorded from unilateral bipolar hippocampal electrodes (Fig. 3A) consisted of polyspikes or sharp-wave trains with an amplitude that was at least twice the background and a duration of >6 s (consistent with the definitions of Galvan et al., 2000, and Nairismagi et al., 2004). As typical for seizures (Franaszczuk et al., 1998; Bragin et al., 1999) the amplitude of these events rose during the event (0.18 ± 0.01 mV at the onset of the 2nd second of the seizure and 0.41 ± 0.01 mV towards the seizure's end; P < 0.0001; paired t-test n = 36), and the frequency of discharges decreased (median frequency during the 2nd second of seizures was 9 Hz, whereas median frequency during the next-to-last second was 7 Hz. Means were 9.0 ± 0.2 Hz and 7.3 ± 0.2 Hz, respectively; P < 0.0001; paired t-test).
The behavioural correlates of these seizures consisted of sudden cessation of activity, accompanied by facial automatisms (stage 1; Racine, 1972). A head-jerk followed by gradual resumption of activity typically signaled the end of the seizure. The EEG changes recorded from unilateral hippocampal leads typically underestimated the duration of the behavioural seizures, and lasted 6–18 s (mean duration 7.8 ± 0.3 s, n = 57; Fig. 3B), consistent with involvement of other limbic regions in the generation of the behavioural phenomena (Ben-Ari et al., 1981). In addition, these hippocampal EEG events were heralded and followed by far more widespread and longer changes in electrographic activity recorded from cortical leads.
In the cortical EEGs, the amplitude decreased substantially starting about half a minute before the hippocampal onset of the seizures (23.9 ± 5.2 s; n = 44). This low amplitude cortical activity endured during the electrographic hippocampal seizures and persisted for 15.2 ± 3.1 s after the apparent end of the paroxysmal hippocampal activity (Fig. 4A). Thus, although the electrographic events recorded from unilateral hippocampal electrodes were short, the overall neuronal disturbance associated with these seizures was substantially longer: reduced amplitude of cortical EEG lasted on average 49 ± 6.4 s, and in some cases up to 4 min (Fig. 4B).
Postictal depression was apparent in hippocampal traces after termination of the seizures (Fig. 5A). This pattern was evident in 50% of rats, and mean duration of this depression was 3.2 ± 0.4 s (Fig. 5B). Note that cortical postictal depression was significantly longer, lasting 15.2 ± 3.1 s (P < 0.05, Fig. 5B).
Spontaneous seizures were already present in the first video-EEG session in 50% of epileptic rats, permitting initial assessment of their progression with time over the 3 month recording period. When feasible, this analysis did not reveal progressive increase of seizure frequency or duration.
Prolonged FS caused interictal events in 15 of 17 rats (88.2%) that were detected primarily during periods of rest. These events were not found in normothermic or hyperthermic control groups, excluding the possibility that they were variants of normal oscillatory activity within hippocampus (Wiest and Nicolelis, 2003; Kelly, 2004). Interictal events were defined using several criteria that clearly distinguished them from seizures: First, when those lasting 4–5 s were analysed, there was no increase of discharge amplitude between the first and last seconds: 0.20 ± 0.01 mV and 0.21 ± 0.01 mV, respectively, n = 26. Frequency of discharges during these events also did not change (8.35 ± 0.32 Hz during the first second versus 8.12 ± 0.31 Hz during the last, n = 26). In addition, the raw spectra of seizures and of interictal events differed: seizures were characterized by a major sharp peak (amplitude >8-fold of basal) of 7 Hz activity, with a minor (~2-fold amplitude increase) additional spike at 23 Hz. In contrast, a similar analysis of the interictal events found a broad ‘hump’ of frequencies at 5–9 Hz, as well as several smaller peaks at ~17–18 Hz, 25 and 26 Hz (data not shown). Both types of events also had components in the gamma, 36–46 Hz range. Thus, the contour of the interictal events was typical of limbic epileptiform interictal discharges, consisting of polyspikes and/or sharp-waves (50–200 ms) in 87% of rats (Fig. 6A). Interestingly, quantitative analysis of the duration of interictal events in epileptic rats (Fig. 6B) revealed a temporal distribution that tended to be consistent for each rat, and different among individual animals (Fig. 6C, e.g. duration of events of rat no. 3 versus nos. 1, 4 or 5, P < 0.05).
We queried whether fundamental neuronal oscillatory activity, outside of periods of frank seizures, was altered by the early-life FS. Therefore, we analysed the raw EEG energy spectra in individual rats that developed spontaneous seizures (n = 6) compared with those manifesting interictal events only (n = 9), and normothermic controls (n = 8). Remarkably, energy spectra of the three groups differed, with a striking reduction of low-frequency (1–10 Hz) energy found in the frankly epileptic rats (Fig. 7). This reduction did not occur in FS-experiencing rats that did not develop spontaneous seizures: in the latter group, energy spectra resembled those of controls.
We have shown previously that experimental prolonged FS lead to transient neuronal injury, but no detectable cell death in hippocampus and amygdala, as well as in limbic cortices (Toth et al., 1998; Bender et al., 2003a). However, in these original studies, we did not distinguish between animals that became epileptic and those that did not. Thus, the question of whether epileptogenesis after prolonged FS is accompanied by (and may require) neuronal loss has not been fully resolved.
This question was addressed in the current study by quantifying neuronal populations specifically in those rats that had developed epilepsy after FS. We chose to examine populations known to be most vulnerable to seizures in animal models of limbic epilepsy (i.e. hilar neurons; Sloviter, 1994), as well as those most affected in human TLE after an early-life precipitating event including prolonged FS (i.e. neurons in Sommer's sector = CA1; Armstrong, 1993). We did not examine neuronal counts in the entorhinal cortex. As shown in Fig. 8, neuronal densities did not differ between the epileptic and the normothermic control group in both the hilus (Fig. 8B; P = 0.16) and CA1 (Fig. 8C; P = 0.93). In addition, no changes of hilar or hippocampal volume were observed that might confound the cell counts (Fig. 8D).
The major findings of these studies are (i) Prolonged experimental FS induce recurrent, spontaneous, behavioural and electrographic (electro-clinical) seizures later in life in 35% of rats (and never in controls). (ii) The ictal events are brief, but perturb normal cortical neuronal activity for significantly longer periods, evident by reduced cortical EEG amplitude. (iii) Fundamental EEG activity of rats rendered epileptic after FS is modified, constituting a potential marker for epileptogenesis after prolonged FS in the human. Taken together, the data indicate that experimental prolonged FS may provoke limbic epilepsy, and may therefore represent a useful model for studying the relationship between FS and human TLE.
Using an established model of early-life prolonged FS (Toth et al., 1998; Brewster et al., 2002; Bender et al., 2003a; Dubé et al., 2004), the current study demonstrates that these convulsions lead to spontaneous hippocampal seizures, i.e. they generate limbic epilepsy. The seizures recorded to date have been brief and were defined as ictal when several conditions coincided: epileptiform hippocampal EEG discharges exceeded 6 s, they were typical of seizure progression, with increasing amplitude and slowing frequency, and were associated with abruptly modified behaviour. The behaviours, in turn, were in accord with those found in human (and experimental) limbic seizures when the seizures are confined to the limbic circuit (Margerison and Corsellis, 1966; Goddard et al., 1969; Racine 1972; Theodore et al., 1983; Williamson et al., 1987). This conservative approach that defined only electro-clinical events involving both behaviour and abnormal neuronal activity as seizures, may have underestimated the number of seizures, because epileptiform EEG activity without clearly evident behavioural changes was observed on occasion.
The events recorded from unilateral hippocampal electrodes in this study were short (6–18 s). In many cases, behavioural changes, typically freezing (Racine-stage 0), preceded the onset of hippocampal discharges by ~1–2 s, and return to normal behaviour was delayed by 2–3 s after termination of hippocampal EEG seizures. This is to be expected if the hippocampus, where the recording electrode was placed, was not the site of origin of the seizures. Indeed, the origin of seizures within the limbic circuit is often outside of the hippocampus (Ben-Ari et al., 1981), not uncommonly in the amygdaloid complex. Therefore, given that we had electrodes only in a single dorsal hippocampus, the apparent dissociation between the onset of the clinical and the EEG onset of the seizures suggests, or is at least consistent with, a seizure origin elsewhere in the limbic circuit. Thus, our results for the duration of these seizures are probably an underestimate.
Whereas most human limbic seizures are longer than the seizure duration recorded here, the minimal duration required to consider epileptic events as seizures is not well defined. In humans, absence seizures are often defined as lasting 3 seconds or longer, and thus leading to apparent alteration of consciousness (International League Against Epilepsy, 1981). In animal models, many definitions exist (Bragin et al., 1999; Galvan et al., 2000; Raol et al., 2003; Nairismagi et al., 2004). In addition, seizures have even been recognized, with no lower limit of duration, also in in vitro systems (Khalilov et al., 2003). Common operational definitions of temporal lobe (limbic) seizures in humans rely on epileptiform EEG activity that suffices to alter behaviour (and/or consciousness). In view of these non-uniform approaches, seizures in the current study have been defined operationally, as ictal events that abruptly influence behaviour. In addition, both parameters, the EEG and the behaviour, have further been subjected to biological-relevance constraints: The EEG activity signifying a seizure must be epileptiform, as conventionally defined (amplitude larger than twice the background, spikes/polyspike contour, progression of both amplitude and frequency). In analogy, the behaviour should be consonant with that exhibited by humans and animals (e.g. early phases of kindling) during verified, well accepted seizures that are confined to the limbic circuit (Goddard et al., 1969; Racine 1972; McIntyre and Kelly, 1993). The events described here meet these conservative criteria, and are thus considered seizures.
The ictal events recorded from hippocampal electrodes were associated with longer and more wide-ranging electrographic changes typical of limbic seizures in humans and animal models: starting about half a minute prior to the onset of hippocampal epileptiform discharges, cortical EEG amplitude suddenly declined. This ‘depression’ persisted during the hippocampal seizures and into the hippocampal postictal period, lasting up to 4 min. In addition, slowing of frontoparietal EEG activity during the seizures occurred in a quarter of the events, reminiscent of ictal slowing in frontal and ipsilateral parietal EEGs of human temporal lobe seizures (Lieb et al., 1991; Blumenfeld et al., 2004). This slowing is considered to derive from surround inhibition of the structures outside the area of seizure onset (Engel et al., 1982; VanLandigham and Lothman, 1991; Schwartz and Bonhoeffer, 2001). In addition, postictal depression, i.e. reduced amplitude of EEG discharges, was evident in hippocampal EEGs in 50% of animals and a third of the ictal events, as found in human postictal EEGs (Ajmone-Marsan and Ralston, 1957; Kaibara and Blume, 1988; Franaszczuk et al., 1998; Olejniczak et al., 2001). These findings suggest that these spontaneous seizures evoked by early-life experimental FS perturbed normal neuronal oscillatory activity in cortical and limbic circuits for substantially longer periods than their apparent duration.
In addition, power spectral analysis of the EEGs of rats that developed spontaneous seizures suggested remarkable alterations in the overall rhythm spectrum of neuronal activity. Thus, EEGs from epileptic rats were characterized by a significant reduction of energy in the low frequencies (1–10 Hz). This was unique to this group, and distinguished it from the group with interictal events alone, where EEG spectra resembled those in controls. Whereas the precise relationship of the loss of the low-frequency oscillation (typically associated with sleep) and the presence of spontaneous seizures is not clear, it is tempting to speculate that the seizures may disrupt these normal brain activities, potentially via alteration of sleep architecture (Besset, 1982; Bazil et al., 2000).
Prolonged FS led to interictal events in 88.2% of the rats (and to frank seizures in 40% of this group). These data suggest that the seizures influenced neuronal inter-communication in the limbic circuit in the majority of animals. Whereas the mechanisms underlying these FS-evoked changes are not well understood, previous studies have excluded potential candidate mechanisms and implicated others. Thus, experimental prolonged FS did not result in death of any of the neuronal populations that are vulnerable to prolonged seizures in adult (Ben-Ari, 1985; Sutula et al., 1988; Sloviter et al., 1994; Pitkänen et al., 2002) and juvenile rats (Sankar et al., 1998; Kubova et al., 2001), or are injured or lost in human TLE (Falconer et al., 1964; Armstrong, 1993; Mathern et al., 2002). Interestingly, transient cytoskeletal changes in several of these populations, including hippocampal CA1 and CA3 pyramidal cells and some hilar neurons were found after experimental FS (Toth et al., 1998). In addition, MRI studies have demonstrated acute T2 signal changes after these seizures in limbic structures, partially overlapping those involved in the cytoskeletal studies. These occurred in a majority of FS-rats, and were not a result of neuronal death (Dubé et al., 2004, Fig. 4).
Whereas the studies described above analysed all animals after experimental FS, here we counted vulnerable neuronal populations specifically in rats that became epileptic after experimental FS, compared with normal controls. Again, we found little evidence of cell loss in the epileptic animals, although, in the absence of rigorous stereological methodology in this study, loss of a minimal number of neurons cannot be absolutely excluded. This lack of significant neuronal loss suggests that other mechanisms, not requiring cell loss, become operative after experimental FS to provoke epilepsy in these animals (Baram et al., 2002). These probably include substantial functional changes in the properties of hippocampal neurons. For example, early and sustained increase in GABAergic inhibition was found in animals that had experienced experimental FS (Chen et al., 1999). Importantly, neuronal excitability was augmented (Dubé et al., 2000) at least in part by increased hyperpolarization-activated current, Ih, promoting rebound depolarization in response to hyperpolarizing input (Chen et al., 2001; Santoro and Baram, 2003). The basis for this increase of Ih, carried by the hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, involved seizure-evoked alteration of expression of HCN channel isoforms, with a consequent change of the current they carry. Enhanced expression of the cyclic-AMP (cAMP) sensitive slow-deactivating HCN2 isoform, reduced expression of the fast-deactivating, relatively cAMP insensitive HCN1, and formation of heteromeric channels composed of these two isoforms probably contribute to augmented hyperpolarization-dependent rebound depolarization in hippocampal neurons (Brewster et al., 2002, 2005; Santoro and Baram, 2003).
This is the first study that directly addresses the causal relationship of long FS and the development of TLE. In the animal model, where predisposing factors, both genetic (e.g. Fernandez et al., 1998; Wallace et al., 2001) and acquired, have largely been excluded, the answer is in the affirmative. However, many caveats and further questions remain. First, spontaneous seizures developed only in a subgroup of rats experiencing prolonged FS (a minimum 35%, although this may be an underestimate, as discussed above), and the reasons are not clear. Whereas occult genetic factors may have not been fully excluded and might contribute to such variability, model-related parameters are more likely to account for the development of epilepsy only in a subset of animals. For example, sub-clinical, longer-duration seizures may have persisted beyond the original hyperthermia-evoked ‘FS’ in some animals, promoting the development of epilepsy. Alternatively, subtle undetected seizures may have recurred during the first few hours after the inciting hyperthermia-induced FS. These questions will be addressed in future studies. Larger group sizes will also better estimate the precise proportion of animals that develop TLE, and, to eliminate the possibility that electro-clinical seizures were missed because the EEG-epileptiform discharges originated from the hemisphere contralateral to that of the recording electrodes, bilateral hippocampal electrodes will be employed, as well as extra-hippocampal (such as amygdala) leads (Gloor, 1991). Finally, whereas the current recordings were prolonged, they were mainly carried out at night and not continuously for weeks and months. The availability of telemetric devices should facilitate future continuous-recording studies. These studies will also permit us to determine the exact time when the ‘pro-epileptic’ EEG features of the seizure-experiencing rats arise.
In summary, this is the first direct study examining the consequences of the most common seizures of childhood on the development of TLE. In this study, prolonged experimental FS provoked limbic (temporal lobe) epilepsy. Therefore, this seizure model provides a powerful tool for further addressing important questions in human epilepsy. These include the mechanisms by which these seizures promote epileptogenesis (Bender et al., 2003b; Dubé et al., 2005b), the presence of markers for this process (Roch et al., 2002; Dubé et al., 2004; Nairismagi et al., 2004), and the potential for interventions in the epileptogenic process (White, 2002).
We thank M. Hinojosa for expert editorial assistance and K. Fenoglio for her help and support. Supported by NIH NS35439, NS49618 and an AES research initiative award (T.Z.B.) and by an Epilepsy Foundation of America postdoctoral research fellowship (C.D.).