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J L Stringer

Publications and source records attributed to J L Stringer.

At least 37 records · Page 2Linked to original sources

Is cell death necessary for hippocampal mossy fiber sprouting?

To examine the relationship between cell death and sprouting of the mossy fibers, repeated seizures of the hippocampal-parahippocampal circuit were elicited in anesthetized rats. The presence of mossy fiber growth was assessed with the Timm's stain for zinc. At 4 weeks, after 18 repeated seizures, there was a significant increase in the degree of zinc containing granules in the inner molecular layer of the dentate gyrus. The amount of sprouting was less than that seen four weeks after a single injection of kainic acid. A silver impregnation stain and an assay for damaged DNA were used to detect damaged or dying neurons and immunohistochemistry for a 72 kDa heat shock protein was used to detect any neurons that had suffered potentially injurious stress. The same number of repeated seizures that caused sprouting of the mossy fibers did not cause detectable cell death or severe stress in any cells within the hippocampus, subicular region or adjacent entorhinal cortex. These experiments demonstrate that repeated seizures of the hippocampal-parahippocampal circuits can cause sprouting of mossy fibers in the absence of evidence of cell death. This supports the hypothesis that alterations in intrinsic neural excitability and impulse activity from the dentate gyrus can result in growth of axonal processes in the adult rat brain.

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Role of potassium and calcium in the generation of cellular bursts in the dentate gyrus.

Epileptiform activity, which appears to be endogenous, has been recorded in the granule cells of the dentate gyrus before the onset of synchronized seizure activity and has been termed cellular bursts. It has been postulated that an increase in input to the dentate gyrus causes a local increase in extracellular K+ concentration ([K+]o) and a decrease in [Ca2+]o that results in this cellular bursting. The first test of this hypothesis is to determine whether the cellular bursts appear in ionic conditions that occur in vivo before the onset of synchronized epileptic activity. This hypothesis was tested in vitro by varying the ionic concentrations in the perfusing solution and recording changes in the granule cells of the dentate gyrus. Intra- and extracellular recordings were made in the dentate gyri of hippocampal slices prepared from anesthetized adult Sprague-Dawley rats. Increasing the extracellular potassium or decreasing the extracellular calcium of the perfusing solution caused three forms of spontaneous activity to appear: depolarizing potentials, action potentials, and cellular bursts. Increasing potassium or decreasing calcium also caused the granule cells to depolarize and reduced their input resistance. No synchronized extracellular field activity was detected. Simultaneously increasing potassium and decreasing calcium caused cellular bursts to appear at concentrations recorded in vivo before the onset of synchronized reverberatory seizure activity.

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Repeated seizures increase GFAP and vimentin in the hippocampus.

Reactive gliosis is a response of astrocytes to a variety of insults that is characterized by hypertrophy of the cell bodies and processes and an increase in the expression of glial fibrillary acidic protein (GFAP). The signal that regulates the transition to the reactive state and the role of vimentin in reactive gliosis are unknown. The experiments here used a model of repeated seizures in the hippocampal-parahippocampal circuits to determine the extent and time course of reactive gliosis, including the appearance of vimentin, in response to seizures. Reactive gliosis, detected by immunohistochemistry for the presence of GFAP and vimentin, was present 2-7 days after the repeated seizures. At least 9 seizures, or at least 250 s of seizure discharge, were needed to induce reactive gliosis. After seizures, cells staining for vimentin were found in the dentate gyrus molecular layer and hilar region, as well as in the molecular layer of CA1. Fewer cells were stained in the CA3 region. These experiments demonstrate that repeated discrete seizures of the hippocampal-parahippocampal circuits can cause reactive gliosis and localized induction of a glial protein (vimentin) that is not normally expressed in the adult brain.

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Influence of osmolality on seizure amplitude and propagation in the rat dentate gyrus.

We tested the role of changes in extracellular space on synchronization and propagation of epileptiform activity in the dentate gyrus in vitro by manipulating the osmolality of the perfusing solution. Increasing the osmolality reduced the amplitude of the population spikes and slowed the propagation of the epileptiform activity. Decreasing the osmolality had the opposite effect. Assuming there were significant changes in the size of the extracellular space, and therefore the ease with which ephaptic interactions can occur, these results support the hypothesis that ephaptic interactions play a role in the synchronization and propagation of epileptic activity in the dentate gyrus.

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During afterdischarges in the young rat in vivo extracellular potassium is not elevated above adult levels.

Studies have suggested that in the immature brain an unusually high ceiling level for potassium may lead to an increased propensity for seizures. In these experiments, the peak levels of extracellular potassium in the hippocampus in vivo were recorded in immature rats 10-27 days old and compared to levels reached in adults. There was no difference in the peak level of potassium attained during an afterdischarge in any of the age groups tested.

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Ethosuximide specifically antagonizes the effect of pentylenetetrazol in the rat entorhinal cortex.

This study tested two related hypotheses. The first is that the entorhinal cortex has an important role in synchronization and spread of epileptiform activity into the dentate gyrus. The second is that ethosuximide acts by antagonizing the action of pentylenetetrazol (PTZ) in the entorhinal cortex. Experiments were carried out in urethane anesthetized rats. Recording electrodes were placed in the dentate gyrus and stimulating electrodes were placed in the angular bundle. Administration of PTZ reduced the time to onset of maximal dentate activation, which is a marker for synchronized reverberatory seizure activity in the hippocampal-parahippocampal circuits. Since PTZ facilitates the spread of epileptiform activity in, or through, the entorhinal cortex, these results support the hypothesis that the entorhinal cortex can influence the spread of seizure activity from the entorhinal cortex into the hippocampus. Ethosuximide specifically, and dose-dependently, reduced the polysynaptic response in the dentate gyrus that is initiated by PTZ, while having no effect on the response in the dentate gyrus to ipsilateral angular bundle stimulation. These results support the hypotheses that ethosuximide can antagonize this effect of PTZ.

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Burst characteristics of dentate gyrus granule cells: evidence for endogenous and nonsynaptic properties.

1. Hippocampal slices bathed in 8 mM potassium and 0-added calcium exhibited spontaneous epileptiform activity in the dentate gyrus. Extracellular recording revealed recurrent prolonged bursts of population spikes and an associated negative DC shift. These episodes were very similar to the in vivo phenomenon termed maximal dentate activation (MDA). Therefore this in vitro activity will be referred to as MDA-like activity or events. 2. During the MDA-like activity, the individual granule cells exhibited a sustained depolarization that matched the duration of the negative extracellular DC shift. At the beginning of the MDA-like activity, there was a burst of action potentials. After the burst, most granule cells either continued to fire action potentials regularly or in bursts. Some cells exhibited this initial burst of activity and then a dramatic reduction in firing rate. This reduction in rate was followed by a gradual increase in the amplitude and frequency of the epileptiform activity recorded during the remainder of the MDA-like event. 3. Before and between MDA-like events, spontaneous cellular activity consisted of single action potentials and bursts of action potentials on a depolarizing envelope. In addition, depolarizing potentials, up to 13 mV, were recorded. There were no extracellular field potentials associated with these intracellularly recorded potentials. 4. In the 8 mM potassium, 0-added calcium test solution, the membrane potential threshold for burst production was significantly lower than in normal potassium and calcium medium. 5. The effect of depolarizing and hyperpolarizing current injections on the amplitude and frequency of the epileptiform activity was tested. Current injection had no effect on the frequency of the epileptiform activity recorded during the MDA-like events. However, the frequency of the cellular bursts between MDA-like events was very sensitive to current injection. Depolarizing current increased the frequency, and hyperpolarizing current decreased the frequency of the spontaneous activity. 6. This study has shown that in 8 mM potassium and 0-added calcium the granule cells of the dentate gyrus are capable of generating spontaneous bursts that appear to be mediated by endogenous mechanisms. In addition, synchronized epileptiform discharges were recorded from the granule cells at regular intervals that appear were recorded from the granule cells at regular intervals that appear to be mediated by exogenous nonsynaptic mechanisms.

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In the hippocampus in vivo, nitric oxide does not appear to function as an endogenous antiepileptic agent.

Using a reverberatory epilepiform discharge of hippocampal-parahippocampal circuits termed "maximal dentate activation", this study investigated whether the local release of nitric oxide within these circuits functions as an antiepileptic agent. Two nitric oxide synthase inhibitors (L-nitro-arginine methyl ester and 7-nitro-indazole) and a guanylate cyclase inhibitor (methylene blue) were tested, and none had a significant effect on the time to onset or duration of maximal dentate activation. A membrane-permeable analogue of cyclic guanosine monophosphate (cGMP), 8-bromo-cGMP, caused an increase in the time to onset and a decrease in the duration of maximal dentate activation. The number of neurons expressing NADPH diaphorase activity (a marker for nitric oxide synthase) was also examined after repeated elicitation of maximal dentate activation. After 18 seizures there was a significant, but transient, decrease in the number of hilar/subgranular neurons that were NADPH diaphorase-positive. The decrease was only seen at 1 h after the last seizure. There was no induction of NADPH diaphorase activity. These results are not consistent with the hypothesis that, in hippocampal-parahippocampal circuits in vivo, nitric oxide is released in response to neuronal activity and then acts to terminate the neuronal activity.

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Pentylenetetrazol causes polysynaptic responses to appear in the dentate gyrus.

In a particular brain region specific changes in inhibition or excitation may be the basis of seizure initiation. Alternatively, changes in the balance of excitation and inhibition in the circuit, which may be detectable as polysynaptic responses may be more important indicators of epileptogenesis. That the appearance of polysynaptic responses precedes the initiation and, therefore, may be necessary for the onset of epileptiform activity in the hippocampal-parahippocampal circuit was tested using the chemical convulsant pentylenetetrazol. Excitation and paired-pulse inhibition were measured in CA1 and the dentate gyrus of the urethane-anaesthetized rat before and after administration of pentylenetetrazol. In addition, three polysynaptic responses were monitored. In both CA1 and the dentate gyrus, pentylenetetrazol, 100 mg/kg, caused a trend towards increased excitability and caused a relatively mild loss of inhibition. Two polysynaptic responses appeared in the dentate gyrus after the administration of pentylenetratrazol, both apparently mediated through the entorhinal cortex. A polysynaptic response of the CA1 pyramidal neurons to contralateral angular bundle stimulation was not observed. These experiments demonstrate that pentylenetetrazol will facilitate only the appearance of polysynaptic responses mediated through the entorhinal cortex. These results support the hypothesis that pentylenetetrazol has a specific action within the entorhinal cortex that may facilitate the synchronization and spread of epileptiform activity. These results are also consistent with the hypothesis that the appearance of polysynaptic responses may be necessary for the onset of epileptogenesis in the hippocampal-parahippocampal circuit.

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Spreading depression and reverberatory seizures induce the upregulation of mRNA for glial fibrillary acidic protein.

The present study evaluates the relative roles of seizure activity and spreading depression in upregulating glial fibrillary acidic protein (GFAP) mRNA expression. Stimulating electrodes were placed bilaterally in the angular bundle, and recording electrodes were placed bilaterally in the dentate gyrus of adult rats. Intense electrographic seizures were induced by delivering stimulus trains through one stimulating electrode. In some cases, spreading depression accompanied the seizures, while in other cases, the seizures occurred in the absence of spreading depression. Animals were killed 24 h following the last stimulus train, and the forebrains were prepared for quantitative in situ hybridization. Seizure activity and spreading depression led to significant increases in GFAP mRNA levels in the hippocampal formation. Seizure activity alone (without spreading depression) induced a 4-fold increase in GFAP mRNA levels in the hilus and molecular layer of the dentate gyrus and in stratum lacunosum-moleculare of the hippocampus. When seizure activity was accompanied by spreading depression, there was a 10-fold increase in GFAP mRNA levels in these same regions. Regional differences within the hippocampal formation in glial cell response were evident. While GFAP mRNA levels in stratum lacunosum-moleculare of the hippocampus were upregulated by seizure activity and spreading depression, levels in hippocampal stratum radiatum of the hippocampus remained unchanged. The results suggest that abnormal neuronal activity can influence glial cell gene expression and that spreading depression is a stronger signal than seizure activity in upregulating GFAP mRNA levels.

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Analysis of field potentials evoked in Ca1 by angular bundle stimulation in the rat.

Anatomical data and in vitro electrophysiological data suggest that entorhinal cortical efferents monosynaptically excite CA1 pyramidal cells. In vivo stimulation of the angular bundle (AB) evokes an extracellular waveform, suggestive of a population spike. Previously, this waveform has been claimed to be activation of the direct entorhinal cortex to CA1 pathway and a volume-conducted response from the dentate gyrus. This study sought to distinguish between these two possibilities using several techniques in urethane anesthetized rats. A comparison of waveforms evoked in the dentate gyrus (DG) and in CA1 by a single-shock test stimulus to the AB revealed that the early positive-to-negative phase of the waveform recorded in CA1 correlated in time and amplitude to the population spike recorded in the DG. When the AB test stimulus was preceded by a single shock to the AB or to the contralateral hilus, the amplitudes of the DG population spike and the early phase of the CA1 waveform decreased equally. Current source density analysis of the response to the AB test stimulus revealed that early current sinks localized only to the DG. Finally, focal application of the local anesthetic tetracaine into CA1 did not decrease the amplitude of the waveform evoked by the AB test stimulus. Tetracaine, however, greatly deceased the population spike evoked in CA1 by stimulating the contralateral CA3. Together these data indicate that the early positive-to-negative phase of the waveform in CA1 evoked by the AB test stimulus reflects events in the DG and not direct activation of CA1 by entorhinal cortical afferents.

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Pentylenetetrazol elicits epileptiform activity in the dentate gyrus of the urethane anesthetized rat by activation of the entorhinal cortex.

Pentylenetetrazol is a chemical convulsant, often used to generate experimental seizures, that is thought to act as a GABA antagonist. In the urethane anesthetized rat, pentylenetetrazol produces a characteristic epileptiform discharge in the dentate gyrus. The hypothesis that this discharge is generated by activity in the entorhinal cortex was examined in this study. Recording electrodes were placed in the dentate gyrus bilaterally and neuronal activity was recorded after administration of pentylenetetrazol. A laminar analysis of the convulsant-induced activity was compared to responses evoked by angular bundle stimulation (n = 6). Both convulsant-induced and evoked activity were negative-going in the molecular layer of the dentate gyrus. In other animals tetrodotoxin (TTX) was injected into the right entorhinal cortex before the onset of epileptiform activity (n = 5). The TTX prevented epileptiform activity in the right dentate gyrus. Injection of TTX after the onset of epileptiform activity caused the epileptiform activity to cease on the side of injection (n = 5). These experiments support the hypothesis that pentylenetetrazol specifically activates the entorhinal cortex to produce the epileptiform activity recorded in the dentate gyrus. This selective activation suggests that the mechanism of action of pentylenetetrazol, as a convulsant, is not simply as an antagonist of GABA receptors.

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Pharmacological characterization of the afterdischarge that precedes the onset of maximal dentate activation in the rat.

Two types of afterdischarges have been recorded in the dentate gyrus after trains of electrical stimulation. The first afterdischarge contains predominantly broad positive potentials. The second afterdischarge contains bursts of large amplitude population spikes and has been termed maximal dentate activation. It has been proposed that the first afterdischarge is a precursor to maximal dentate activation and, therefore, it is termed a pre-MDA afterdischarge. The effects of several drugs on these afterdischarges were compared in adult male rats anesthetized with urethane. Stimulus trains (50 Hz) designed to elicit the pre-MDA afterdischarge were administered to the left CA3 region while recording in the ipsilateral dentate gyrus and contralateral CA1 cell layer. Phenytoin (80 mg/kg), phenobarbital (60 mg/kg), ethosuximide (300 mg/kg) and sodium valproate (300 mg/kg) had no effect on the duration or characteristics of the discharge. Carbamazepine (50-60 mg/kg) and ketamine (30 mg/kg) reversibly blocked the discharge. Diazepam (3 mg/kg) reduced the duration of the discharge and also reduced the amplitude of population spikes recorded in CA1. Baclofen (10 mg/kg) and bicuculline (0.5 mg/kg) increased the duration of the discharge. The effects of dizocilpine (MK-801, 2 mg/kg) were inconsistent. These results were compared to the effects of the same drugs on the time-to-onset and duration of maximal dentate activation. The pharmacological sensitivities of maximal dentate activation and pre-MDA discharges were found to be qualitatively different.

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Kainic acid, bicuculline, pentylenetetrazol and pilocarpine elicit maximal dentate activation in the anesthetized rat.

Patterns of epileptiform activity in the hippocampus induced by chemical convulsants were recorded in the urethane-anesthetized rat. Previously, two epileptiform discharges have been recorded in the dentate gyrus after electrical stimulation, one consisting of broad positive potentials and the second consisting of bursts of large amplitude population spikes (termed maximal dentate activation). In the present study, convulsant-induced epileptiform activity was documented and compared to stimulus-evoked activity. Four systemically active convulsants--kainic acid, bicuculline, pentylenetetrazol and pilocarpine--were used in this study. One of the convulsants was administered and the animal was monitored for the development of epileptiform activity in CA1, CA3 and the dentate gyrus. The epileptiform activity that first appeared after each of the convulsants was grouped into four categories. With extended monitoring, or an increase in dose, each of the chemical convulsants produced maximal dentate activation in the majority of the animals tested (72-90%). When maximal dentate activation was present bursts of population spikes were also recorded in CA3 and CA1. These observations suggest that the early discharges are related to the mechanism of action of the convulsant and that the appearance of maximal dentate activation is independent of the mechanism of action. In addition, there does not appear to be a fixed evolution of epileptic discharges in these circuits when comparing seizure induction by different mechanisms.

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Valproic acid and ethosuximide slow the onset of maximal dentate activation in the rat hippocampus.

Valproic acid and ethosuximide are commonly used to treat absence seizures, but their mechanisms of action have not been clearly defined. This is partly due to testing in different experimental models and different species. We re-examined the effect of valproic acid and ethosuximide in an experimental model of reverberatory seizures in the hippocampus of the urethane-anesthetized rat, maximal dentate activation. Valproic acid, at 450 and 600 mg/kg i.p., caused an increase in the time to onset of seizure discharges, but only the changes with 600 mg/kg reached statistical significance. Both doses of valproic acid shortened the seizure duration. Serum levels of valproic acid were determined and it appears that in this system at least 200-400 micrograms/ml are needed to produce an effect on seizure onset and duration. Ethosuximide, at 600 mg/kg i.p., delayed the onset of the seizure discharge and blocked the increase in seizure duration. Both ethosuximide and valproic acid delayed the onset of the seizure discharge in this model suggesting that these drugs may help to determine the mechanisms behind seizure initiation in the hippocampal-parahippocampal circuits.

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Repeated seizures cause a generalized increase in excitability in the hippocampus.

Changes in excitability within the hippocampus were examined by recording in CA3 and in CA1 or the dentate gyrus and stimulating in the angular bundle (fiber bundle connecting the entorhinal cortex with the dentate gyrus) before and after 36 electrographic seizures in urethane anesthetized rats. The responses recorded in CA3 or CA1 to stimulation of the angular bundle every 30 s were unchanged after repeated seizures, while the responses in the dentate gyrus were augmented. When the angular bundle was stimulated every 200 ms, population spikes appeared in CA3 and CA1, with CA1 producing multiple population spikes before CA3. The results indicate that after repeated seizures there is a general enhancement of excitability throughout the hippocampus.

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Alterations in both excitation and inhibition occur before the onset of seizure activity in the hippocampus.

Excitatory and inhibitory mechanisms have been implicated in the onset of seizures and as underlying kindling. In this study, changes in responses to single stimuli and paired pulse stimuli were used to monitor postsynaptic excitability before the onset of seizure activity in limbic circuits of urethane-anesthetized rats. With sufficient stimulus intensity, a stimulus paradigm of seven pulses every second for 10 s led to seizure activity, as indicated by the appearance of maximal dentate activation, and afterdischarges. An increase in the evoked response was found in both CA1 and the dentate gyrus during stimulus trains to either CA3 or the angular bundle and there was the appearance of a polysynaptic response. There was an increase in paired pulse inhibition in the dentate gyrus and a decrease in paired pulse inhibition in the CA1 region during the stimulus protocol. Since repeated seizures and a number of pharmacological agents are known to alter the onset and duration of seizure activity, a relationship between the changes in excitability and the onset of the seizure activity was tested using MK-801, ketamine, bicuculline, diazepam, phenobarbital, baclofen and repeated seizures. Overall, alteration of the amplitude of the polysynaptic response in CA1 to angular bundle stimulation correlated best with the effects of the drugs and the seizures on the duration of maximal dentate activation.

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Ontogeny of hippocampal afterdischarges in the urethane-anesthetized rat.

Experimental studies have shown that seizure manifestations vary as the brain develops. This study investigated the characteristics of afterdischarges in the hippocampal circuits at various ages in the developing rat. Rats from the following post-natal periods were tested: PN 10-11, PN 14-15, PN 17-19, PN 21-23 and PN 25-27. Animals were anesthetized with urethane and recording electrodes placed in the hippocampus bilaterally. Stimulating electrodes were placed in the left CA3 region and in the angular bundle. Afterdischarges were produced in all animals using stimulus trains of 20 or 50 Hz. Rats in the PN 10-11 and 14-15 age groups had afterdischarges that consisted of population spikes in CA1 and broad positive potentials in the dentate gyrus. Between PN 17 and 19, maximal dentate activation, which consists of bursts of large amplitude population spikes in the dentate gyrus, first appeared in response to 20 Hz stimulation to CA3 or either 20 or 50 Hz stimulation to the angular bundle. Rats older than 21 days had afterdischarge patterns like those recorded in the adult. These data indicate that, in the rat, the seizure capabilities of the limbic circuits go through a major transition period around PN 17-19. The appearance of maximal dentate activation marks the ability of the developing rat brain to produce and sustain reverberatory seizure discharges.

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