The objective of this proposal is to identify mechanisms involved in the suppression of seizures as a function of age. The increased seizure susceptibility of the immature brain may be due to absence of networks that develop with age and ultimately suppress seizures in adults Ongoing studies suggest that in the adult substantia nigra (SN) there are two topographically discrete GABAA- sensitive regions which differ in the mRNA expression of the GABAA receptor alpha subunit. These two regions alter metabolism in divergent ngral projections and mediate opposing effects on seizures demonstrating the existence of separate anticonvulsant and proconvulsant SN networks. This nigral topographic arrangement occurs with maturation. It is not present in two week old rats in which only the proconvulsant system is functioning.
The first aim i s to determine in adult rats the characteristics of the two GABAA sensitive nigral networks by determining the localization, connectivity and characteristics of the neurons in the regions that mediate the opposing nigral effects on seizures and whether the effects of the two regions on seizures are specific for the GABAA- system.
The second aim i s to determine the maturational patterns of the two networks in rats of various ages until the establishment of the adult features. Methods include localized microinfusions of GABAA, GABAB or excitatory aminoacids -agonists and antagonists and seizure testing using flurothyl, [3H] autoradiography, immunocytochemistry, tracing techniques, [14C] deoxyglucose autoradiography and in vitro receptor binding. Rats of various ages throughout development will be used to determine the maturational profIle of the SN seizure modification. The goal is to develop a better understanding of the mechanisms that participate in the suppression of seizures with maturation. These studies may lead to the development of new therapeutic treatments that will compensate for the maturational state of the CNS.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS020253-10
Application #
2263819
Study Section
Neurology A Study Section (NEUA)
Project Start
1984-09-30
Project End
2002-02-28
Budget Start
1995-04-01
Budget End
1996-02-29
Support Year
10
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Neurology
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Galanopoulou, Aristea S; Mowrey, Wenzhu B; Liu, Wei et al. (2017) Preclinical Screening for Treatments for Infantile Spasms in the Multiple Hit Rat Model of Infantile Spasms: An Update. Neurochem Res 42:1949-1961
Shandra, Oleksii; Moshé, Solomon L; Galanopoulou, Aristea S (2017) Inflammation in Epileptic Encephalopathies. Adv Protein Chem Struct Biol 108:59-84
Nariai, Hiroki; Beal, Jules; Galanopoulou, Aristea S et al. (2017) Scalp EEG Ictal gamma and beta activity during infantile spasms: Evidence of focality. Epilepsia 58:882-892
Galanopoulou, Aristea S; Moshé, Solomon L (2015) Neonatal and Infantile Epilepsy: Acquired and Genetic Models. Cold Spring Harb Perspect Med 6:a022707
Sánchez Fernández, Iván; Loddenkemper, Tobias; Galanopoulou, Aristea S et al. (2015) Should epileptiform discharges be treated? Epilepsia 56:1492-504
Akman, Ozlem; Moshé, Solomon L; Galanopoulou, Aristea S (2015) Early life status epilepticus and stress have distinct and sex-specific effects on learning, subsequent seizure outcomes, including anticonvulsant response to phenobarbital. CNS Neurosci Ther 21:181-92
Akman, Ozlem; Gulcebi, Medine I; Carcak, Nihan et al. (2015) The role of the substantia nigra pars reticulata in kindling resistance in rats with genetic absence epilepsy. Epilepsia 56:1793-802
Shinnar, Shlomo; Cnaan, Avital; Hu, Fengming et al. (2015) Long-term outcomes of generalized tonic-clonic seizures in a childhood absence epilepsy trial. Neurology 85:1108-14
Galanopoulou, Aristea S; Moshé, Solomon L (2015) Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies. Neurobiol Dis 79:135-49
Jette, Nathalie; Beghi, Ettore; Hesdorffer, Dale et al. (2015) ICD coding for epilepsy: past, present, and future--a report by the International League Against Epilepsy Task Force on ICD codes in epilepsy. Epilepsia 56:348-55

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