Use-dependent intrinsic plasticity in the cerebellum

描述(由申请人提供)：现代记忆存储理论主要集中于突触功能的持续性、经验依赖性变化，如长时突触增强和抑制(LTP&LTD)。这些现象在记忆模型中很有吸引力，部分原因是它们通常表现出某种程度的突触专一性，允许非常大量的独立可修改的单位，因此也就是非常大的存储容量。除了这些突触变化外，现在还出现了证据表明，内在神经元兴奋性的持续变化，即我们所说的“内在可塑性”，是由行为动物的某些形式的训练以及脑片和神经元培养中的人工激活模式产生的。这些内在变化可以作为记忆本身的一部分，或者作为相关现象，例如记忆的巩固或自适应概括的触发，尤其是非陈述性记忆。几年前，我们发表了第一份关于大脑内在兴奋性持续突触驱动变化的报告。这是在小脑深核(DON)中的一个区域，它是某些任务(如联合眼皮调节)记忆存储的中心区域。自那以后，我们对诱导要求和这一现象的表达进行了广泛的参数描述。在这里，我们建议通过研究DCN内在可塑性的细胞和分子基础来扩展这些初步观察。首先，我们希望描述参与内在可塑性的受体，特别是谷氨酸、5-羟色胺和去甲肾上腺素的受体。其次，我们将讨论第二信使级联的作用，包括蛋白激酶、磷酸酶、脂肪酶和钙库。第三，我们将通过记录和闭塞实验来寻找参与本征可塑性表达的特定离子通道(S)。第四，我们将使用共聚焦成像和非聚焦来确定固有可塑性的空间范围。这是一项基础研究，旨在解决记忆存储背后的分子机制，使用一个异常明确的模型系统。希望这项工作将有助于创造记忆疾病的治疗和诊断方法。因为这些细胞和分子过程不仅涉及记忆存储，这项工作也对其他大脑疾病有影响，包括癫痫和成瘾。

DESCRIPTION (provided by applicant): Modern theories of memory storage have largely focused on persistent, experience-dependent changes in synaptic function such as long-term synaptic potentiation and depression (LTP & LTD). These phenomena are appealing in models of memory, in part because they typically display some degree of synapse-specificity, allowing for a very large number of independently modifiable units and, consequently, a very large storage capacity. In addition to these synaptic changes, evidence has now emerged for persistent changes in intrinsic neuronal excitability, what we call "intrinsic plasticity", produced by certain forms of training in behaving animals and artificial patterns of activation in brain slices and neuronal cultures. These intrinsic changes may function as a portion of the engram itself, or as a related phenomenon such as a trigger for the consolidation or adaptive generalization of memories, particularly non-declarative memories. Several years ago, we published the first report of persistent synaptically driven changes in intrinsic excitability in the brain. This, in the deep cerebellar nuclei (DON), a region which is central to memory storage for certain tasks such as associative eyelid conditioning. We have since performed an extensive parametric description of the induction requirements and the expression of this phenomenon. Here, we propose to extend these initial observations by investigating the cellular and molecular basis of intrinsic plasticity in the DCN. First, we wish to characterize the receptors involved in intrinsic plasticity with particular emphasis on receptors for glutamate, serotonin and norepinephrine. Second, we will address the role of second messenger cascades including protein kinases, phosphatases, lipases and Ca stores. Third, we shall seek to identify the particular ion channel(s) involved in the expression of intrinsic plasticity through recording and occlusion experiments. Fourth, we shall use confocal imaging and uncaging to determine the spatial extent of intrinsic plasticity. This is basic research to address the molecular mechanisms that underlie memory storage, using an unusually well-defined model system. It is hoped that this work will be useful for creating therapies and diagnostics for diseases of memory. Because these cellular and molecular processes are not only involved in memory storage, this work has implications for other brain diseases as well, including epilepsy and addiction.