Linden D J, Murakami K, Routtenberg A
Brain Res. 1986 Aug 6;379(2):358-63. doi: 10.1016/0006-8993(86)90790-0.
Protein kinase C can be activated by oleate, an unsaturated fatty acid. Since protein kinase C is activated by long-term potentiation, we wished to determine whether iontophoretic ejection of oleate into the intact hippocampal dentate gyrus of urethane-anesthetized rats would cause an enhancement of the response potentiated by high frequency stimulation of the perforant path. Oleate ejection did significantly enhance the persistence of the potentiated response. Moreover, a growth of the response beyond the initial potentiation was seen. Arachidonate, which stimulates protein kinase C to a lesser degree, had a significant preservation effect, but no effect on growth of the response. After vehicle and elaidate (trans-stereoisomer of oleate) ejections, the potentiated response decayed to baseline values. In addition, the persistence of the potentiated response observed two hours after its induction was positively correlated with the ability of an unsaturated fatty acid to activate protein kinase C in vitro. The present results support the proposal that protein kinase C activation enhances synaptic strength. It is suggested that one mechanism for this activation may be PLA2-mediated release of oleate.
蛋白激酶C可被不饱和脂肪酸油酸激活。由于蛋白激酶C可被长时程增强激活,我们希望确定将油酸离子导入到经氨基甲酸乙酯麻醉的大鼠完整海马齿状回中,是否会增强由穿通路径高频刺激所增强的反应。油酸导入确实显著增强了增强反应的持续性。此外,还观察到反应在初始增强之外有所增长。花生四烯酸对蛋白激酶C的刺激程度较小,它具有显著的保护作用,但对反应增长没有影响。在注入溶剂和反油酸(油酸的反式立体异构体)后,增强反应衰减至基线值。此外,增强反应诱导两小时后观察到的持续性与不饱和脂肪酸在体外激活蛋白激酶C的能力呈正相关。目前的结果支持蛋白激酶C激活增强突触强度这一观点。有人提出,这种激活的一种机制可能是磷脂酶A2介导的油酸释放。