Pentylenetetrazol-induced seizures are associated with Na+,K+-ATPase activity decrease and alpha subunit phosphorylation state in the mice cerebral cortex

被引:14
|
作者
Marquezan, Barbara P. [1 ]
Funck, Vinicius R. [1 ]
Oliveira, Clarissa V. [1 ]
Pereira, Leticia M. [1 ]
Araujo, Stifani M. [2 ]
Zarzecki, Micheli S. [2 ]
Royes, Luiz Fernando F. [1 ,3 ]
Furian, Ana Flavia [1 ,4 ]
Oliveira, Mauro S. [1 ,2 ]
机构
[1] Univ Fed Santa Maria, Dept Physiol & Pharmacol, Pharmacol Grad Program, BR-97105900 Santa Maria, RS, Brazil
[2] Fed Univ Pampa Itaqui, BR-97650000 Itaqui, Brazil
[3] Univ Fed Santa Maria, Dept Sports Methods & Tech, BR-97105900 Santa Maria, RS, Brazil
[4] Univ Fed Santa Maria, Dept Food Technol & Sci, BR-97105900 Santa Maria, RS, Brazil
关键词
Sodium pump; Epilepsy; Convulsion; Phosphorylation; NA+-K+-ATPASE; PATHWAY; EPILEPSY; ISOFORM; PUMP;
D O I
10.1016/j.eplepsyres.2013.03.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The present study aimed to investigate whether Na+,K+-ATPase activity and phosphorylation state of the catalytic alpha subunit are altered by pentylenetetrazol (PTZ)-induced seizures. PTZ (30, 45 or 60 g/kg, i.p.) was administered to adult male Swiss mice, and Na+,K+-ATPase activity and phosphorylation state were measured in the cerebral cortex 15 min after PTZ administration. Na+,K+-ATPase activity significantly decreased after PTZ-induced seizures (60 mg/kg). Immunoreactivity of phosphorylated Ser943 at alpha subunit was increased after PTZ-induced seizures. A significant positive correlation between Na+,K+-ATPase activity and latency to myoclonic jerks and generalized seizures was found. Conversely, a strong negative correlation between Ser943 phosphorylation and latency to generalized seizures was detected. Given the role of Na+,K+-ATPase as a major regulator of brain excitability, Ser943 at Na+,K+-ATPase a subunit may represent a potentially valuable new target for drug development for seizure disorders. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:396 / 400
页数:5
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