Motor seizures were induced by intraperitoneally (i.p.) injected bicuculline in 270 rats aged 7, 12, 18, 25, or 90 days. Bicuculline was able to elicit both minimal (clonic) and major (tonic-clonic) seizures in all age groups, but in 7-day-old rats minimal seizures were only noted exceptionally. CD50s (for major seizures) ranged from 2.48 to 2.85 mg/kg in the three younger groups and increased to approximately 7 mg/kg in 25- and 90-day-old rats. An intravenous (i.v.) administration of bicuculline in 67 rats, 18 and 25 days old, caused identical CD50s in these groups, indicating that the difference that occurs with an i.p. administration is due to pharmacokinetic reasons. Electrocorticographic (ECoG) studies in acute experiments as well as in young rats with implanted electrodes demonstrated general principles of the development of EEG: an increase in frequency of individual elements, in generalization of the epileptic activity, in synchronization of activity among various cortical regions, and in the correlation between ECoG and motor phenomena. An exception occurred as an age-related phenomenon: rhythmic activity of the spike-and-wave type. This activity appeared in 18-day-old and older rats and was invariably accompanied by "freezing" of the animals.
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http://dx.doi.org/10.1111/j.1528-1157.1989.tb05332.x | DOI Listing |
Brain Commun
January 2025
Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.
Developmental and epileptic encephalopathies constitute a group of severe epilepsies, with seizure onset typically occurring in infancy or childhood, and diverse clinical manifestations, including neurodevelopmental deficits and multimorbidities. Many have genetic aetiologies, identified in up to 50% of individuals. Whilst classically considered paediatric disorders, most are compatible with survival into adulthood, but their adult phenotypes remain inadequately understood.
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December 2024
Department of Pathology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Brain edema and neurological symptoms are the hallmarks of the uncommon disease known as posterior reversible encephalopathy syndrome (PRES), which can have several etiological causes. Since the etiology determines the course of treatment, diagnosis is crucial. There have only been 14 cases of PRES associated with inflammatory bowel disorders documented.
View Article and Find Full Text PDFFront Pharmacol
January 2025
Department of Neuroscience, Washington University in St. Louis, St. Louis, MO, United States.
The Kv3.2 subfamily of voltage activated potassium channels encoded by the gene is abundantly expressed in neurons that fire trains of fast action potentials that are a major source of cortical inhibition. Gain-of-function (GOF) pathogenic variants in and , encoding Kv3.
View Article and Find Full Text PDFActa Biomater
January 2025
Key Laboratory of Neuropharmacology and Translational Medicine of Zhejiang Province, School of Pharmaceutical Sciences and School of Basic Medical Sciences, Huzhou Central Hospital, The Fifth School of Clinical Medicine of Zhejiang Chinese Medical University, Zhejiang Chinese Medical University, Hangzhou, China. Electronic address:
Epilepsy is a common neurological disease characterized by distinct pathological changes in the epileptogenic zone. Antiseizure drugs (ASDs) are widely used as the primary treatment for epilepsy. To improve the efficiency of ASDs medication, stimuli-responsive nanoscale drug delivery systems (nanoDDSs), triggered by either endogenous or exogenous factors, have been developed and been considered as a noninvasive and spatial-temporal approach to epilepsy theranostics.
View Article and Find Full Text PDFNeurosurgery
January 2025
Department of Biomedical Sciences, Humanitas University, Milan, Italy.
Background And Objectives: Understanding and managing seizure activity is crucial in neuro-oncology, especially for highly epileptogenic lesions like isocitrate dehydrogenase (IDH)-mutant gliomas. Advanced MRI techniques such as diffusion tensor imaging (DTI) and neurite orientation dispersion and density imaging (NODDI) have been used to describe microstructural changes associated with epilepsy. However, their role in tumor-related epilepsy (TRE) remains unclear.
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