Relationship between susceptibility to dmcm-induced generalized motor convulsions and low-affinity [h-3]-ouabain binding in membranes in rat brain

Relationship between susceptibility to dmcm-induced generalized motor convulsions and low-affinity [h-3]-ouabain binding in membranes in rat brain

Author Contó, Marcos Brandao Autor UNIFESP Google Scholar
Campana Venditti, Marco Antonio Autor UNIFESP Google Scholar
Abstract Background and Objective: Epilepsy is one of the most prevalent neurological disorders worldwide, but its underlying mechanisms have not yet been clarified. Among the possible molecular mechanisms that underlie its occurrence are those that are responsible for the neuronal ionic gradient, including the transmembrane enzyme Na+, K+-adenosine triphosphatase (ATPase). Na+, K+-ATPase plays an important role in controlling neuronal excitability, and it is believed to be related to the pathophysiology of epilepsy. However, the specific isozymes that may be related to this neurological disorder remain to be determined. The 3 subunit-containing Na+, K+-ATPase isozyme has high affinity for ouabain and appears to play a major role in the pathogenesis of epilepsies. However, more studies are needed to evaluate the possible participation of Na+, K(+)ATPase isozymes with lower affinity for ouabain (i.e., those that contain the 1 and 2 subunits). Methods: The present study investigated whether rats with high (HTR) and low (LTR) thresholds for clonic convulsions that are induced by a benzodiazepine inverse agonist differ in the binding of [H-3]ouabain to Na+, K+-ATPase isozymes with lower affinity to ouabain in discrete brain regions. Results: Compared with the HTR group, the LTR group exhibited lower binding of [H-3]-ouabain in the brainstem and frontal cortex. Conclusion: This finding supports the hypothesis that epilepsy is associated with impairments in Na+, K(+)ATPase activity. The results also suggest that Na+, K+-ATPase isozymes that contain the 1/2 subunits in these brain regions may underlie the susceptibility to methyl 6,7-dimethoxy-4-ethyl-beta-carboline-3-carboxylate-induced convulsions.
Keywords Benzodiazepine Inverse Agonist
Epilepsy
Generalized Motor Convulsions
Low-Affinity [H-3]-ouabain Binding
Na+,K+-Atpase Isozymes
Ouabain
SeizuresK+-Atpase Activity
Ouabain Binding
Quantitative Autoradiography
Alpha-3 Isoforms
Sodium-Pump
Na+
Seizures
Mice
Hippocampus
Thresholds
Language English
Sponsor Associacao Fundo de Incentivo a Pesquisa (AFIP)
Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
Grant number Contó, Marcos Brandao [UNIFESP]
Venditti, Marco Antonio Campana [UNIFESP]
Date 2016
Published in Current Molecular Pharmacology. Sharjah, v. 9, n. 4, p. 332-336, 2016.
ISSN 1874-4672 (Sherpa/Romeo, impact factor)
Publisher Wiley
Extent 332-336
Origin http://dx.doi.org/10.2174/1874467209666160408152558
Access rights Closed access
Type Article
Web of Science ID WOS:000406220600008
URI http://repositorio.unifesp.br/handle/11600/49227

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