首页> 外文期刊>The Journal of Physiology >An experimental test of the role of postsynaptic calcium levels in determining synaptic strength using perirhinal cortex of rat.
【24h】

An experimental test of the role of postsynaptic calcium levels in determining synaptic strength using perirhinal cortex of rat.

机译:实验性的实验,通过使用大鼠的周围神经皮层,评估突触后钙水平在确定突触强度中的作用。

获取原文
获取原文并翻译 | 示例
           

摘要

1. We have investigated the prediction of a relationship between the magnitude of activity-dependent increases in postsynaptic calcium and both the magnitude and direction of synaptic plastic change in the central nervous system. 2. Activity-dependent increases in calcium were buffered to differing degrees using a range of concentrations of EGTA and the effects on synaptic plasticity were assessed. Activity-dependent synaptic plasticity was induced during whole-cell recording in rat perirhinal cortex in vitro. In control conditions (0.5 mM EGTA) low frequency stimulation (LFS; 200 stimuli) delivered to neurones held at -40 or -70 mV induced long-term depression (LTD) or, at -10 mV, induced long-term potentiation (LTP). 3. The relationship between EGTA concentration (0.2 to 10 mM) and the magnitude of LTD was examined. This relationship described a U-shaped curve, as predicted by models of synaptic plasticity. This provides strong evidence that the magnitude of LTD is determined by the magnitude of the increase in intracellular calcium concentration. 4. LFS paired with depolarisation to -10 mV induced LTD, no change or LTP as activity-dependent postsynaptic calcium levels were allowed to increase progressively by the use of progressively lower concentrations of buffer (10 to 0.2 mM EGTA). 5. We investigated if the lack of plasticity that occurs at the transition between LTD and LTP is due to induction of both of these processes with zero net change, or is due to neither LTD nor LTP being induced. These experiments were possible as LTP but not LTD was blocked by the protein kinase inhibitor staurosporine while LTD but not LTP was blocked by the mGlu receptor antagonist MCPG. At the transition between LTD and LTP, blocking LTP mechanisms did not uncover LTD whilst blocking LTD mechanisms did not uncover LTP. This suggests that the transition between LTD and LTP is due to the lack of induction of both of these processes and also suggests that these two processes are induced independently of one another.
机译:1.我们研究了中枢神经系统中突触后钙的活动依赖性增加幅度与突触可塑性变化的幅度和方向之间的关系的预测。 2.使用一系列浓度的EGTA将钙的活性依赖性增加缓冲至不同程度,并评估其对突触可塑性的影响。依赖活动的突触可塑性在体外大鼠全周皮层皮质全细胞记录中被诱导。在控制条件下(0.5 mM EGTA),将低频刺激(LFS; 200刺激)传递给保持在-40或-70 mV的神经元引起的长期抑郁(LTD)或在-10 mV的神经元引起的长期增强(LTP) )。 3.检查了EGTA浓度(0.2至10mM)和LTD的大小之间的关系。正如突触可塑性模型所预测的,这种关系描述了一个U形曲线。这提供了有力的证据表明LTD的大小取决于细胞内钙浓度增加的大小。 4. LFS与去极化至-10 mV诱导的LTD配对,通过使用逐渐降低的浓度的缓冲液(10至0.2 mM EGTA),可以使活性依赖性突触后钙水平逐渐升高或保持不变。 5.我们调查了LTD和LTP之间过渡时发生的可塑性不足是由于这两个过程的净变化为零引起的,还是归因于LTD和LTP均未引起。这些实验是可能的,因为LTP不受蛋白激酶抑制剂星形孢菌素的阻滞,而LTD不受LG受到mGlu受体拮抗剂MCPG的阻滞。在LTD和LTP之间的过渡过程中,阻止LTP机制未发现LTD,而阻止LTD机制未发现LTP。这表明LTD和LTP之间的过渡是由于缺少这两个过程的诱导,也表明这两个过程是相互独立诱导的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号