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

机译:戊四唑诱发的癫痫发作与小鼠大脑皮层的Na +,K + -ATPase活性降低和α亚基磷酸化状态有关

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摘要

The present study aimed to investigate whether Na+,K+-ATPase activity and phosphorylation state of the catalytic α subunit are altered by pentylenetetrazol (PTZ)-induced seizures. PTZ (30, 45 or 60g/kg, i.p.) was administered to adult male Swiss mice, and Na+,K+-ATPase activity and phosphorylation state were measured in the cerebral cortex 15min after PTZ administration. Na+,K+-ATPase activity significantly decreased after PTZ-induced seizures (60mg/kg). Immunoreactivity of phosphorylated Ser943 at α 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 α subunit may represent a potentially valuable new target for drug development for seizure disorders.
机译:本研究旨在研究戊四唑(PTZ)诱导的癫痫发作是否改变了Na +,K + -ATPase活性和催化α亚基的磷酸化状态。给成年的雄性瑞士小鼠施用PTZ(30、45或60g / kg,腹膜内),并在施用PTZ 15分钟后测量大脑皮层中的Na +,K + -ATPase活性和磷酸化状态。 PTZ诱发癫痫发作后(60mg / kg),Na +,K + -ATPase活性显着降低。 PTZ诱发的癫痫发作后,磷酸化的Ser943对α亚基的免疫反应性增加。发现Na +,K + -ATPase活性与肌阵挛性抽搐潜伏期和全身性癫痫发作之间呈显着正相关。相反,检测到Ser943磷酸化与潜伏期与广泛性癫痫发作之间存在很强的负相关性。鉴于Na +,K + -ATPase是大脑兴奋性的主要调节剂,Na +,K + -ATPaseα亚基的Ser943可能代表了癫痫病药物开发的潜在有价值的新靶标。

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