Instituto de Biología Celular y Neurociencias Prof E De Robertis, CONICET-UBA, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina.
Neurochem Res. 2011 Feb;36(2):297-303. doi: 10.1007/s11064-010-0317-x. Epub 2010 Nov 16.
The expression of Na(+), K(+)-ATPase α3 subunit and synaptosomal membrane Na(+), K(+)-ATPase activity were analyzed after administration of ouabain and endobain E, respectively commercial and endogenous Na(+), K(+)-ATPase inhibitors. Wistar rats received intracerebroventricularly ouabain or endobain E dissolved in saline solution or Tris-HCl, respectively or the vehicles (controls). Two days later, animals were decapitated, cerebral cortex and hippocampus removed and crude and synaptosomal membrane fractions were isolated. Western blot analysis showed that Na(+), K(+)-ATPase α3 subunit expression increased roughly 40% after administration of 10 or 100 nmoles ouabain in cerebral cortex but remained unaltered in hippocampus. After administration of 10 μl endobain E (1 μl = 28 mg tissue) Na(+), K(+)-ATPase α3 subunit enhanced 130% in cerebral cortex and 103% in hippocampus. The activity of Na(+), K(+)-ATPase in cortical synaptosomal membranes diminished or increased after administration of ouabain or endobain E, respectively. It is concluded that Na(+), K(+)-ATPase inhibitors modify differentially the expression of Na(+), K(+)-ATPase α3 subunit and enzyme activity, most likely involving compensatory mechanisms.
Na(+)、K(+) - ATPase α3 亚基的表达和突触体膜 Na(+)、K(+) - ATPase 活性在分别给予哇巴因和内源性 Na(+)、K(+) - ATPase 抑制剂 endobain E 后进行了分析。Wistar 大鼠分别经脑室给予哇巴因或内源性 Na(+)、K(+) - ATPase 抑制剂 endobain E(溶解于生理盐水或 Tris-HCl 中)或其载体(对照)。两天后,处死动物,取出大脑皮质和海马,分离粗制和突触体膜部分。Western blot 分析显示,给予 10 或 100nmoles 哇巴因后,大脑皮质中 Na(+)、K(+) - ATPase α3 亚基的表达增加了约 40%,而海马中则保持不变。给予 10μl endobain E(1μl = 28mg 组织)后,大脑皮质中 Na(+)、K(+) - ATPase α3 亚基增加了 130%,海马中增加了 103%。给予哇巴因或内源性 Na(+)、K(+) - ATPase 抑制剂 endobain E 后,皮质突触体膜中的 Na(+)、K(+) - ATPase 活性降低或升高。结论是,Na(+)、K(+) - ATPase 抑制剂可差异调节 Na(+)、K(+) - ATPase α3 亚基和酶活性的表达,很可能涉及补偿机制。