Sokolova N E, Malikov U M, Kuznetsov V L, Emel'yanov N A
Laboratory of Functional Neurochemistry, I. P. Pavlov Institute of Physiology, Russian Academy of Sciences, St. Petersburg, Russia.
Neurosci Behav Physiol. 1998 Sep-Oct;28(5):500-3. doi: 10.1007/BF02463009.
Existing data on the role of Ca2+ ions in the development of long-term potentiation were used as a basis for studying changes in different Ca2+ compartments in cells in living rat olfactory cortex slices during potentiation. The kinetics of 45Ca2+ exchange were studied at 5, 15, and 30 min of potentiation. During the induction phase (1-5 min) of long-term potentiation, the fraction of tightly-bound intracellular Ca2+ decreased. There were no changes in the content of Ca2+ ions in other fractions at this stage. During maintenance of potentiation, which lasted 15-25 min, Ca2+ levels in the extracellular and intracellular compartments did not differ from controls. At 30 min, during extinction of long-term potentiation, there was a significant redistribution of Ca2+ in cells: the levels of free and loosely-bound Ca increased, as did extracellular Ca2+.
关于钙离子在长时程增强作用发展中作用的现有数据,被用作研究在增强过程中活体大鼠嗅皮质切片细胞中不同钙离子区室变化的基础。在增强作用的5分钟、15分钟和30分钟时研究了45Ca2+交换的动力学。在长时程增强作用的诱导阶段(1 - 5分钟),紧密结合的细胞内钙离子比例下降。在此阶段,其他组分中钙离子含量没有变化。在持续15 - 25分钟的增强作用维持期间,细胞外和细胞内区室的钙离子水平与对照无差异。在30分钟时,在长时程增强作用消退期间,细胞内钙离子发生了显著的重新分布:游离和松散结合的钙离子水平增加,细胞外钙离子水平也增加。