Glebov R N, Kryzhanovskiĭ G N, Malikova L A, Rodina V I, Rozhanets V V, Sandalov I U
Biokhimiia. 1976 Jul;41(6):975-81.
Electric stimulation (EC) of a suspension of native synaptic membranes of rat brain cortex in the Krebs-Ringer-glucose medium revealed Ca-dependent inhibition of Na+, K+-ATPase and inhibition of transport Ca-activated, Mg-dependent ATPase. The effects observed are not induced by a change in the SH-groups of the membrane proteins and are removed by an addition of total lipids of the brain (membrane protein: lipid = 5:1) or 0.35 mM novocaine. Cyclic 3',5'-AMP in concentrations of 0.1--1.0 mM causes an inhibition (up to 50%) of Na+, K+-ATPase of native synaptic membranes. The Na+, K+-ATPase activity of purified membrane preparations is not changed either by the cyclic nucleotide, or by EC. It is assumed that depolarization of excitable membranes results in structural changes, mediated by the activation of protein kinase, and manifesting themselves as labilization of protein-lipid ratios.
在Krebs - Ringer - 葡萄糖培养基中对大鼠大脑皮层天然突触膜悬浮液进行电刺激(EC),结果显示Ca依赖性抑制Na⁺、K⁺ - ATP酶以及抑制钙激活的、Mg依赖性ATP酶的转运。所观察到的这些效应并非由膜蛋白的SH基团变化所诱导,并且通过添加脑总脂质(膜蛋白:脂质 = 5:1)或0.35 mM奴夫卡因可消除这些效应。浓度为0.1 - 1.0 mM的环3',5'-AMP会导致天然突触膜的Na⁺、K⁺ - ATP酶受到抑制(高达50%)。纯化膜制剂的Na⁺、K⁺ - ATP酶活性既不会因环核苷酸也不会因电刺激而改变。据推测,可兴奋膜的去极化会导致结构变化,这种变化由蛋白激酶的激活介导,并表现为蛋白质 - 脂质比率的不稳定。