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Query: UMLS:C0036572 (seizures)
 80,221 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. Three different cortical areas were found with respect to the development, by repeated electrical stimulation, of electrographic and motor seizures in rats. Paleocortical areas responded similarly to subcorticallimbic structures. Initial after-discharges (ADs) were accompanied by little or no behavioral response. With spaced reptition ADs became longer, propagated more strongly, and were eventually accompanied by a convulsive response in which the dominant components were forelimb clonus and rearing. Anterior neocortical placements, on the other hand, yielded convulsive responses from the first AD. These convulsive responses became stronger with repeated stimulation until a mild form of extension was triggered. ADs remained relatively short. Posterior neocortical areas showed electrographic developments very similar to those found in anterior neocortical areas but convulsive responses never developed. 2. All areas tested showed similar reductions in AD thresholds when repeatedly stimulated. Initial thresholds were lower in paleocortical than in neocortical areas. 3. Motor seizures developed more rapidly with stimulation of contralateral homologous sites after seizures had been developed in the primary (initially stimulated) focus. AD thresholds, on the other hand, were not significantly affected in contralateral sites after being lowered in primary sites.
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PMID:Modification of seizure activity by electrical stimulation: cortical areas. 4 98

Procaine HCl and diphenylhydantoin (DPH) increased the duration and propagation of epileptiform afterdischarges (ADs) produced by electrical stimulation of the amygdala in rats. Procaine and DPH also increased the rate of seizure development (kindling) produced by repeated stimulation of the amygdala. Procaine and to a limited extentDPH would themselves act as convulsants in well kindled subjects. Diazepam, on the other hand, retarded or blocked amygdaloid kindling. Diazepam trigered a high frequency (20-30 c/sec) rhtthm in the amygdala, hippocampus and preoptic area. None of these drugs had any significant effect on potentials evoked in secondary limbic sites by single electrical pulses applied to the amygdala. Also, none of these drugs had any effect on recruiting or post-tetanic potentiation (PTP) in secondary sites produced by amygdala stimulation and none of the drugs had any effect on amygdaloid AD thresholds. The effects of these drugs on the responses evoked by anterior neocortex stimulation were quite different. Diazepam had no effect on any of the characteristics of the discharge or convulsion even at twice the dose levels used for the amygdala group. Procaine and DPH, however, blocked not only the eonvulsion but the AD as well. Eighty percent of the procaine- and DPH-treated rats failed to respond with neocortical AD even at current levels as high as 2000 muA. The few cortically stimulated subjects that did respond with an AD showed a subcortical rather than a neocortical seizure response. DPH had no effect on recruiting or PTP of the transcallosal response. Both procaine and DPH produced a weak but significant increase in the amplitude of the transcallosal evoked potential, while diazepam produce a weak decrement in that response.
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PMID:Effects of procaine hydrochloride, diazepam, and diphenylhydantoin on seizure development in cortical and subcortical structures in rats. 4 16

The effects of cerebellar stimulation were studied in monkeys with chronic alumina-cream epileptogenic foci in motor cortex. Low-frequency stimulation (5-15 c/sec) was ineffective in altering spontaneous cortical spiking. Clinical and electrographic seizures were elicited following high-frequency cerebellar stimulation (100 c/sec). This was a consistent finding following cerebellar stimulation, although no spontaneous seizures had been seen in these animals. These studies suggest the existence of facilitatory cerebellar mechanisms and indicate the need for further studies in chronic animal models.
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PMID:Cortical seizures following cerebellar stimulation in primates. 4 22

Late-onset chronic progressive panencephalitis developed in a 12-year-old boy with congenital rubella syndrome from whose brain rubella virus was isolated. Progressive dementia began at eight, and ataxia, choreiform movements, myoclonic seizures, and fine perimacular pigmentation appeared at 11 years of age. The cerebrospinal fluid was minimally pleocytotic and had a total protein of 156 mg per deciliter, of which 52 per cent was gamma globulin. Electroencephalography demonstrated generalized medium and occasional high-voltage slowing without burst suppression. The antibody titer to rubella virus (hemagglutination inhibition) was 1:8192 in serum and 1:256 in cerebrospinal fluid. Antibody titer to measles virus (complement fixation) was less than 1:8 in serum. Microscopical study of biopsied brain tissue at the age of 11 disclosed panencephalitis similar to subacute sclerosing panencephalitis, but with perivascular deposits and without inclusion bodies. Rubella virus was isolated from the brain by cocultivation with CV-1 cells.
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PMID:Chronic progressive panencephalitis due to rubella virus simulating subacute sclerosing panencephalitis. 4 49

Fifty infants and young preschool children seen in a pediatric developmental service and diagnosed as having "autism" all had evidence of organic disease of the brain and three fourths had mental deficiency of varying degrees. They did not differ in any respect from a comparison group of patients with central nervous system dysfunction unassociated with the symptom complex of autism. Both groups of patients had a high incidence of low birthweight, complications of pregnancy and the neonatal period, seizure disorders, and a variety of specific disease entities associated with developmental defects. Follow-up of 40 of the 45 survivors for a mean of five years showed that none of the patients had had treatment directed to their psychotic symptoms. However, three fourths had established social responses appropriate to their level of function; those who did not generally were over 3 years of age at the time of their first examination or had initial DQs of 35 or less. The degree of mental deficiency was as great or greater at follow-up than it was initially.
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PMID:Some etiologic and prognostic factors in early infantile autism and psychosis. 4 57

Temporal-lobe epilepsy commonly has its origins in childhood, particularly when the lesion involved is mesial temporal (Ammon's horn) Sclerosis. Evidence suggests that this lesion is probably a common cause of chronic epilepsy in adults and that often it is probably the result of a severe febrile convulsion in infancy. 40 children, fifteen years of age and younger, who had an anterior temporal lobectomy were followed up for one to twenty-four years. The findings confirm those already established in adults, that the best results of surgery, not only in seizure relief but also in behaviour, are obtained when mesial temporal sclerosis is the lesion found at operation, and also indicate that a severe febrile convulsion in infancy is often the chief provocative factor in the development of epilepsy.
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PMID:Outcome of surgery in 40 children with temporal-lobe epilepsy. 4 95

Four cases, given in some detail, illustrate the effort to compare scalp EEGs taken before surgery for intractable seizures with those recorded some years postoperatively, and to relate these, together with the computer analyses of seizure activity recorded in depth, with the pathology found in the removed tissue and, importantly, with the postoperative clinical state of the patient. These four cases illustrate the following results: (1) Confirmation by histology and ultrastructure studies of abnormal neuronal tissue at the site pinpointed by computer analysis of EEGs as the driving focus for the electrical seizure discharge. (2) Correlation of clinical and behavioral improvement with normalization of the EEG, objectively quantified by computer analysis. Examples are given of excellent recovery (3 cases) and one of, at present, partial recovery.
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PMID:Long term follow-up of EEG changes following therapeutic surgery in epilepsy. 5 Jan 73

EEG recordings have been made from freely moving, seizure sensitive gerbils during seizures of varying severity. The localization of seizure activity in various brain areas and the generalization of this activity could be correlated with the observed motor manifestations. Paroxysmal observed motor manifestations. Paroxysmal bursting has also been recorded in the parietal cortex of a xeizure sensitive animal in which no concomitant peripheral motor activity was evident. These observations strengthen the suggestion that selectively bred epileptic strains of Meriones unguiculatus may be a suitable animal model for the study of the epilepsies.
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PMID:The Mongolian gerbil (Meriones unguiculatus) as a model for the study of the epilepsies: EEG records of seizures. 5 Jan 85

Fifty-five patients with intractable partial seizures whose on-medication EEGs demonstrated either predominantly focal epileptiform lesions or absence of paroxysmal activity, were studied, and the effect of withdrawing all anticonvulsive drugs on their EEGs was observed. Four types of response were encountered: (1) no effect (20%); (2) specific (focal) activation (25%); (3) complex activation (29%) with widespread of the initial on-medication focus or appearance of the additional independent epileptogenic foci; and (4) "non-specific" activation (63%), consisting of bursts of either bilaterally synchronous and frontally dominant spike and waves, triphasic waves, or sharp slow complexes, or smaller amplitude rapid and diffuse spike-and-wave complexes. This latter effect is thought to be secondary to metabolic derangements resulting from the withdrawal of neurotropic agents and not directly related to the specific epileptogenic process. No association was found between type of effect and any of the following parameters: topography of on-medication focus, duration of therapy, type of anticonvulsant used, suspected underlying etiopathology, or median age when medication was withdrawnn. Furthermore no evidence could be found that the development of a "complex" or "non-specific" EEG effect carried with it a bad prognosis for surgical cure following focal cortical excision. Performing off-medication tracings seems to be of greatest value in patients with partial seizures and EEGs revealing either a relative paucity of definite absence of epileptiform discharges. The occurrence of a "non-specific" response in a questionable epileptic during the off-medication period, on the other hand, should be interpreted with caution.
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PMID:EEG changes after withdrawal of medication in epileptic patients. 5 Feb 14

Potentials evoked in the hippocampus and preoptic region of rats by single biphasic pulses applied to the amygdala were compared during recruiting, after post-tetanic potentiation (PTP) and after amygdaloid kindling. The same components were enhanced temporarily by recruiting and PTP as were enhanced permanently by kindling. Trains of tetanic stimulation with parameters which partially mimicked the cellular discharge parameters during an amygdaloid afterdischarge (AD) were applied to the amygdala at a frequency of 1 per 5 sec continuously for 2.5 h or for 15 min a day for 10 days to produce a total of 1800 trains. Amygdaloid kindling rates were then measured and compared with control groups. Animals pretreated with tetanic stimulation required significantly fewer ADs to develop maximal seizures. Further experiments showed that tetanic stimulation, but not recruiting stimulation (10 c/sec), low frequency stimulation (1 c/sec), or handling, would produce a permanent change in potentials evoked in secondary sites by single pulses applied to the amygdala. This change in evoked potential amplitude was significant but smaller than that produced by kindling. Also tetanic stimulation, but not recruiting or single pulses, facilitated subsequent kindling.
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PMID:Post-activation potentiation and the kindling phenomenon. 5 Feb 24


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