- Research article
- Open Access
Gamma oscillation underlies hyperthermia-induced epileptiform-like spikes in immature rat hippocampal slices
© Wu et al; licensee BioMed Central Ltd. 2001
- Received: 24 September 2001
- Accepted: 28 November 2001
- Published: 28 November 2001
Recently a hyperthermic rat hippocampal slice model system has been used to investigate febrile seizure pathophysiology. Our previous data indicates that heating immature rat hippocampal slices from 34 to 41°C in an interface chamber induced epileptiform-like population spikes accompanied by a spreading depression (SD). This may serve as an in vitro model of febrile seizures.
In this study, we further investigate cellular mechanisms of hyperthermia-induced initial population spike activity. We hypothesized that GABAA receptor-mediated 30–100 Hz γ oscillations underlie some aspects of the hyperthermic population spike activity. In 24 rat hippocampal slices, the hyperthermic population spike activity occurred at an average frequency of 45.9 ± 14.9 Hz (Mean ± SE, range = 21–79 Hz, n = 24), which does not differ significantly from the frequency of post-tetanic γ oscillations (47.1 ± 14.9 Hz, n = 34) in the same system. High intensity tetanic stimulation induces hippocampal neuronal discharges followed by a slow SD that has the magnitude and time course of the SD, which resembles hyperthermic responses. Both post-tetanic γ oscillations and hyperthermic population spike activity can be blocked completely by a specific GABAA receptor blocker, bicuculline (5–20 μM). Bath-apply kynurenic acid (7 mM) blocks synaptic transmission, but fails to prevent hyperthermic population spikes, while intracellular diffusion of QX-314 (30 mM) abolishes spikes and produces a smooth depolarization in intracellular recording.
These results suggest that the GABAA receptor-governed γ oscillations underlie the hyperthermic population spike activity in immature hippocampal slices.
- Hippocampal Slice
- Febrile Seizure
- Spreading Depression
- Population Spike
- Kynurenic Acid
Febrile seizures are the most prevalent type of seizures experienced by children, affecting up to 5% of the world's population . Although most febrile seizures are benign and do not require treatment, they are distressing to parents, and in a few circumstances, can increase the risk of subsequent epilepsy . In clinical practice, therapy for febrile seizures presently is unsatisfactory, since clinical data are insufficient to document efficacy of most anti-epileptic drugs . The most commonly used drug, phenobarbital, has significant deleterious effects on learning and behavior.
A better understanding of the underlying mechanisms of febrile seizures might lead to new strategies of prevention or treatment . Recent work has identified several genes associated with familial febrile seizure tendencies [5–7]. Some of these genes code for ion channels that govern excitability of nerve tissue. We recently published a study of the characteristic hyperthermic responses represented as epileptiform-like population spike activity accompanied by spreading depression (SD) in a rat hippocampal slice, which may serve as an in vitro model of febrile seizures . The hyperthermic response was age-dependent, occurring almost exclusively in young, but not newborn, rats. The primary underlying abnormality in this model was inability of neuronal tissue properly to regulate extracellular potassium concentrations. During heating of the slice, extracellular potassium concentrations rose transiently from the normal 5 mM to as high as 40 mM and extracellular field potential shitted about 20 mV negative, a reversible condition known as SD. During the early phases of SD, neurons burst synchronously in a pattern analogous to seizures. Since hyperthermic epileptiform-like population bursts exhibited the frequency of γ oscillations (30–100 Hz), we hypothesized that GABAA receptor-governed γ oscillations might underlie the cellular basis of hyperthermic epileptiform-like population spike activity.
The γ frequency oscillations (30–100 Hz) are characteristic of responses to sensory input measured by cortical EEG . In the hippocampal slice preparation, γ oscillations can be evoked by brief, high frequency tetanic stimuli to region CA1 [10–13]. The extracellular field potential response during these oscillations takes the form of a train of population spikes in stratum pyramidal at γ and β (15–30 Hz) frequencies . Intracellular recordings during γ oscillations induced by tetanic stimulation reveal a slow membrane depolarization in conjunction with GABAA receptor-mediated inhibitory postsynaptic potentials [11, 15]. This synaptic inhibition-based γ activity entrains action potential generation in pyramidal neurons, leading to the population spikes at γ band frequencies. The specific GABAA receptor antagonist, bicuculline, blocks the γ oscillations [14, 16], an action that can be modeled by simulated neuronal networks . The γ band oscillations appear to play an important role in generation of ictal epileptiform activity in hippocampal slices . This study explores the role of γ oscillations in epileptiform activity in the hyperthermic rat hippocampal slice.
Hyperthermia-induced epileptiform-like population spike activity
Comparison of post-tetanic γ oscillation and hyperthermic population spike activity
Effects of high intensity tetanic stimulation
Effects of bicuculline
Effects of kynurenic acid and QX 314
This study suggests that GABAA receptor-governed γ oscillations underlie the hyperthermic population spike activity in immature hippocampal slices.
Gamma oscillations underlie hyperthermic epileptiform-like population spikes
Gamma oscillations are defined as coherent cortical oscillations at γ (30–100 Hz) band frequency frequencies in in vivo and in vitro models. In hippocampal slice preparations, γ oscillations can be triggered by high frequency tetanic stimuli, called post-tetanic γ oscillations [10–13]. In addition to post-tetanic γ oscillations, the γ oscillations also can be elicited by metabotropic glutamate receptor agonists, carbacol, or free extracellular Mg2+[18, 19]. In this study, we report that γ oscillations can occur in a model of a clinical disorder, namely hyperthermia. Hyperthermic epileptiform-like population spikes occur within the band of γ frequencies (30–100 Hz). Post-tetanic γ oscillations can be mimicked by hyperthermic stimulation in the same slice. Tetanic stimulation at high intensity induces initial γ oscillations followed by a slow SD which resembles hyperthermic epileptiform-like population spikes followed by a slow SD. Finally, both post-tetanic γ oscillations and hyperthermic epileptiform-like population spikes were completely blocked by a GABAA receptor antagonist, BMI. This experimental evidence suggests that the GABAA receptor-governed γ oscillations underlie the hyperthermic population spikes in our in vitro model system.
Possible mechanisms of hyperthermic γ oscillation
Accumulating lines of evidence demonstrate that the genesis mechanisms for post-tetanic γ oscillations involve slow GABAA receptor-mediated depolarization, extracellular K+ elevation and field effects [10–13]. The present study showed that these three major factors also underlie hyperthermic γ oscillations. As shown in Fig. 1A and 2A, the hyperthermic γ oscillations always overlie the slow membrane depolarizations. For post-tetanic γ oscillations, the slow depolarizations were mediated by tetanic stimulation-induced GABAergic depolarizing action [20–23]. This GABAergic depolarization is attributed to the tetanic stimulation-induced accumulation of intracellular chloride  and extracellular potassium . For hyperthermic γ oscillations, heating causes a Na+/K+ pump failure , in turn resulting in the accumulation of intracellular Na+ and Cl-, as well as extracellular K+, finally causing a slow membrane depolarization. In our previous report, the extracellular K+ indeed elevated dramatically during hyperthermia-induced epileptiform-like population spikes and SDs . Field effects further contribute to post-tetanic γ oscillations [25, 26]. High Frequency tetanic stimuli leads to cellular swelling [27, 28], increasing extracellular resistance. According to Ohm's law, this increases the voltage deflection recorded for a given current flowing through this extracellular resistance. Current generated by the active population travels through the resistances of the extracellular space and of the nearby inactive cells, therefore producing the extracellular population spikes and meanwhile depolarizing the inactive cells. In this manner, inactive cells are brought closer to threshold, enhancing their opportunity to firing together [29–31]. The extracellular resistance is the major determinant of field-effect strength . Since the extracellular volume fraction in CA1 stradium pyramidal is only 12% compared with approximately 18% in CA3 and granule cells , the CA1 pyramidal cells are particularly susceptible to field effects. The accumulation of extracellular K+ during hyperthermic SDs depolarizes membrane potential, which triggers initial γ oscillations. Cell swelling reduces the extracellular space, which triggers slow SDs , (Fig. 1A and 2A). In Fig. 6A, after blockade of synaptic transmission by kynurenic acid (7 mM), heating the slice still induced γ-oscillation followed by SD, suggesting that a non-synaptic mechanism (local field effect) may be involved in the generation of hyperthermic γ-oscillations and SDs. Figure 6B demonstrated that hyperthermic γ-oscillations disappear in the presence of an intracellularly delivered Na+ channel blocker (QX 314, 30 mM).
Gamma oscillations and seizures
Epileptic activity can result from an imbalance between glutamatergic excitation and GABAergic inhibition. However, this simple balance model has been challenged by findings that GABAergic transmission remains effective in some epilepsy models, in epileptogenic human tissue [34–40], and by current findings of the excitatory effects of GABA [18, 22, 23]. Therefore, the GABA excitatory effects may work as a possible ictogenic mechanism under some special condition such as tetanic stimulation. Indeed, recently Köhling et al. reported that under epileptogenic condition (free Mg 2+ in ACSF), γ band oscillations arise from GABAergic depolarizations and that this activity may lead to the generation of ictal discharges . It has been reported that prolonged periods of γ oscillations are associated with temporal lobe seizures in in vivo rats . Furthermore, human EEG studies with subdural recording electodes showed that a γ band oscillation could be recorded at the start of typical seizure activity . In this respect, the hyperthermic γ oscillations may also play a critical role in generation of neuronal epileptiform activity. The extent to which the hyperthermic slice serves as a model of febrile seizures remains to be determined. If γ oscillations do prove to be important in clinical febrile seizures, then future work might profitably examine the therapeutic potential of mild disinhibition to disrupt inhibitory GABA-mediated synchrony at the start of ictal activity.
In the in vitro hippocampal slice preparation, hyperthermia-induced epileptiform-like population spikes are at γ band frequencies, and can be blocked by BMI. Therefore, the GABAA receptor-governed γ oscillations underlie the hyperthermic population spikes in immature hippocampal slices.
Experiments were performed on transverse hippocampal slices prepared from Sprague-Dawley rats, ages 17 to 29 days. Rats were anesthetized with halothane and decapitated. The brain tissue was removed rapidly and placed in iced artificial cerebrospinal fluid (ACSF). Brain tissue was then glued to a cryotome, and a few 450–500 μ transverse slices were cut through the hippocampal formations. Slices were allowed to incubate and recover for at least an hour in room temperature ACSF comprised of the following composition (mM): NaCl 117; KCl 5.4; NaHCO3 26; MgSO4 1.3; NaH2PO4 1.2; CaCl2 2.5; glucose 10, continuously bubbled with 95% O2 plus 5% CO2.
Slice were transferred one at a time to the recording chamber (FST, air-liquid interface chamber), and suspended on nylon net at the interface. Carbogen (95% O2 plus 5% CO2) was bubbled across the upper surface of the slice. Temperature was regulated by a feedback circuit, accurate to 0.5 ± 0.2°C. Baseline temperature was 34°C. After verification of evoked population spike stability for three consecutive stimuli over a time course of 15–30 minutes, bath temperature set-point was increased to 41°C and notation was made of actual temperature measured by a thermistor probe.
Extracellular field potentials were recorded with a borosilicate glass micropipette pulled to a tip diameter of 1 μ, filled with 2 M sodium chloride and with resistance approximately 1–10 MΩ. Intracellular recordings were performed with a pulled-glass fine tip micropipette (< 1 μ), with resistance approximately 80–110 MΩ, filled with 4 M potassium acetate. Hyperthermic spreading depressions (SDs) were considered to have occurred when all of the following conditions were met: 1. At least 10 mV extracellular negativity; 2. Duration of extracellular negativity at the half-height of at least 10 seconds; 3. Loss of evoked field in CA1; and recovery of field to at least 50% of control amplitude within 30 minutes of cooling to baseline temperature. Electrophysiological data were stored on a computer (Axon scope), and played back on a laser printer. Slow potentials, including extracellular field during SD also were recorded on a continuous rectilinear chart recorder. To measure oscillation frequency, we chose a slice oscillation range beginning at 200 ms, then used the "frequency count" function of the Origin program to get average frequency from each slice. Chemicals used in the experiment consisted of bicuculline methiodide (BMI), kynurenic acid (Sigma, St. Louis, MO) and QX-314 (Tocris). All animal experiments were in accord with Institutional animal welfare committee guidelines.
All authors were supported by the Marjorie Newsome and Sandra Solheim Aiken Funds for Epilepsy and the Womens' Board of the Barrow Neurological Institute. RSF was supported by the Maslah Saul Chair and the James and Carrie Anderson Laboratory fund for epilepsy research.
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