Xiang J Z, Morton J, Brammer M J, Campbell I C
Department of Neuroscience, Institute of Psychiatry, London, England.
J Neurochem. 1990 Jul;55(1):303-10. doi: 10.1111/j.1471-4159.1990.tb08852.x.
The relationship between intrasynaptosomal total (CaT) and free ([Ca2+]i) calcium and 45Ca accumulation was studied under physiological and K(+)-depolarised conditions in rat cortical synaptosomes. Under physiological conditions, CaT (10.7 mM) was approximately 10,000 times higher than [Ca2+]i (118 nM), showing that there is a large reservoir of sequestered calcium in synaptosomes. 45Ca accumulation was rapid (initial rate, 3.4 nmol/mg protein/min), substantial (7 nmol/mg protein in 2 min), and depolarisation dependent, and reached equilibrium after 5 min. At equilibrium, only 10% of CaT was freely exchangeable. This pool was much larger than the free Ca2+ pool. CaT, [Ca2+]i, and 45Ca accumulations were directly related to the Ca2+ concentration in the buffer, suggesting that [Ca2+]i is not highly conserved but is maintained by simple equilibria between the various pools. Clonidine reduced 45Ca accumulation in a time- and dose-dependent manner. Maximum inhibition (40% at 100 microM) occurred at 2 min and the IC50 was 80 nM. The reduction caused by clonidine (1 microM) reached equilibrium after 5 min, but this equilibrium value was lower than in controls, suggesting that clonidine changes the exchangeable Ca2+ pool size. The effects of clonidine (1 microM) on [Ca2+]i (26% reduction) and on 45Ca accumulation (24% reduction) were most apparent under physiological conditions. However, while it was not dependent on depolarisation, it did not occur in physiological buffer containing low K+ concentration (0.1-1 mM). The inhibitory effect of clonidine on 45Ca accumulation is receptor mediated as it was antagonised by idazoxan (1 microM).(ABSTRACT TRUNCATED AT 250 WORDS)
在大鼠皮质突触体的生理条件和钾离子去极化条件下,研究了突触体内总钙(CaT)、游离钙([Ca2+]i)与45Ca积累之间的关系。在生理条件下,CaT(10.7 mM)比[Ca2+]i(118 nM)高约10000倍,表明突触体中存在大量的钙储存库。45Ca积累迅速(初始速率为3.4 nmol/mg蛋白/分钟)、大量(2分钟内达到7 nmol/mg蛋白)且依赖去极化,5分钟后达到平衡。在平衡时,只有10%的CaT可自由交换。这个池比游离Ca2+池大得多。CaT、[Ca2+]i和45Ca积累与缓冲液中的Ca2+浓度直接相关,表明[Ca2+]i并非高度保守,而是通过不同池之间的简单平衡来维持。可乐定以时间和剂量依赖的方式降低45Ca积累。最大抑制(100 microM时为40%)在2分钟时出现,IC50为80 nM。可乐定(1 microM)引起的降低在5分钟后达到平衡,但该平衡值低于对照组,表明可乐定改变了可交换Ca2+池的大小。可乐定(1 microM)对[Ca2+]i(降低26%)和45Ca积累(降低24%)的影响在生理条件下最为明显。然而,虽然它不依赖于去极化,但在含有低K+浓度(0.1 - 1 mM)的生理缓冲液中不会发生。可乐定对45Ca积累的抑制作用是由受体介导的,因为它可被咪唑克生(1 microM)拮抗。(摘要截断于250字)