Effects of Calcium on the GABAA-Coupled CI-/HCO3- -ATPase from Plasma Membrane of Rat Brain

S. Menzikov, M. Kalinina
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引用次数: 2

Abstract

The work is a study of the influence of Ca2+ (0.01 - 1 mM) on neuronal CI-, HCO3-, -ATPase complex: an enzyme that is a CI--pump which is functionally and structurally coupled to GABAA-receptors. It is found that influence of Ca2+ on the multifunctional complex starts at concentration of 50·M and at concentration of 0.1 mM, it reduces the “basal” one and increases the CI-, HCO3-, -stimulated Mg2+-ATPase activities. GABA (0.1 - 100μM) activates the “basal” Mg2+-ATPase activity in the ab-sence of calcium. The effect of GABA on the enzyme in the presence of 0.01 ·M Ca2+ does not change. At the same time, 1 mM Ca2+eliminates the GABA effect on the “basal” Mg2+-ATPase activity. Competitive blocker of GABAA-receptors bicuculline (5 - 20 μM) in the absence of Ca2+ ions elimi-nates the stimulation of the “basal” Mg2+-ATPase by anions. When 0.25 mM Ca2+ is added to the in-cubation medium the inhibitory bicuculline effect on the enzyme does not appear. We found that 0.1 mM o-vanadate (protein tyrosine phosphatase blocker) reduces the GABA-activated ATPase activity. At the same time, 0.1 mM genistein (a protein tyrosine kinase blocker) has no effect on enzyme activity. In the presence of Ca2+ (0.25 mM), the effect of o-vanadate on the “basal” and CI-, HCO3-, -ATPase activities does not appear. It is shown for the first time that high concentrations of Ca2+prevent the action of GABAA-ergic ligands on the study ATPase. It is assumed that there is the involvement of protein kinases and protein phosphatases in the modulation of the enzyme activity by calcium. The observed effect of calcium on the ATPase may play an important role in the study of the mechanisms of epileptogenesis and seizure activity.
钙对大鼠脑质膜gabaa偶联CI-/HCO3- - atp酶的影响
这项工作是研究Ca2+ (0.01 - 1 mM)对神经元CI-, HCO3-, - atp酶复合物的影响:一种酶,是一种CI泵,在功能和结构上与gabaa受体偶联。发现Ca2+对多功能复合物的影响始于50·M浓度和0.1 mM浓度,降低了“基础”,增加了CI-、HCO3-、-刺激的Mg2+- atp酶活性。GABA (0.1 ~ 100μM)可激活无钙Mg2+- atp酶的“基础”活性。在0.01·M Ca2+存在的情况下,GABA对酶的影响没有变化。同时,1 mM Ca2+消除了GABA对“基础”Mg2+- atp酶活性的影响。gabaa受体的竞争性阻滞剂双管碱(5 - 20 μM)在缺乏Ca2+离子的情况下消除了阴离子对“基础”Mg2+- atp酶的刺激。当培养液中加入0.25 mM Ca2+时,对酶的抑制作用不出现。我们发现0.1 mM o-钒酸盐(蛋白酪氨酸磷酸酶阻滞剂)降低了gaba激活的atp酶活性。同时,0.1 mM染料木素(一种蛋白酪氨酸激酶阻滞剂)对酶活性无影响。在Ca2+ (0.25 mM)存在的情况下,o-钒酸盐对“基础”和CI-、HCO3-、- atp酶活性的影响没有出现。这是第一次表明高浓度的Ca2+阻止gabaa -能配体对研究atp酶的作用。据推测,钙对酶活性的调节有蛋白激酶和蛋白磷酸酶的参与。观察到的钙对atp酶的影响可能在癫痫发生和发作活动机制的研究中起重要作用。
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