Cholinergic signaling in cortical neurons: a unifying hypothesis

描述（由申请人提供）：乙酰胆碱（ACh）在认知中起关键作用，并且对大脑皮层的胆碱能输入减少有助于在阿尔茨海默氏病、路易体痴呆、帕金森氏痴呆和其他神经系统疾病中观察到的认知缺陷。然而，缺乏有关胆碱能作用的药理学或乙酰胆碱影响神经元活性的机制的知识，阻碍了这些衰弱性疾病的特异性治疗方法的发展。现有的数据似乎相互矛盾，难以调和。事实上，乙酰胆碱在提供大部分皮层输出的深层锥体神经元中产生两种相反的反应：快速的短暂抑制和持久的兴奋。虽然介导这些神经元中抑制性胆碱能反应的机制（M1样毒蕈碱乙酰胆碱受体激活、细胞内钙储存的钙释放和随后的SK型钙激活钾传导的激活）已得到很好的描述，但介导胆碱能兴奋的机制以及兴奋性和抑制性胆碱能信号传导之间的功能关系仍然未知。该项目旨在确定受体亚型，信号级联，和离子机制负责胆碱能兴奋在皮层第5层锥体神经元，并测试的总体假设，乙酰胆碱的兴奋性行动反映激活的钙渗透性非选择性阳离子电导，功能上的作用，以补充细胞内的钙存储门抑制胆碱能信号。我们建议在脑切片制备中使用电生理和成像方法来解决以下三个具体目标：1。鉴定新皮层第5层锥体神经元中介导胆碱能兴奋和抑制的特异性毒蕈碱受体。2.确定负责第5层神经元胆碱能兴奋的信号级联和离子机制。3.为了验证兴奋性胆碱能电导在功能上用于补充抑制性胆碱能信号期间耗尽的细胞内钙库的统一假设。我们的研究结果将为理解胆碱能促进认知功能的生物学基础提供一个框架。这些新知识将增加我们对胆碱能系统功能障碍导致痴呆和其他疾病状态中观察到的功能缺陷的理解，并将为治疗干预提供新的靶点。公共卫生相关性：乙酰胆碱是正常认知功能所必需的大脑化学物质，乙酰胆碱的丧失与阿尔茨海默病和其他疾病状态有关。该项目将确定乙酰胆碱影响正常大脑皮层神经元活动的生物学机制，目的是了解为什么衰老或疾病期间乙酰胆碱的丧失会导致认知功能障碍。

DESCRIPTION (provided by applicant): Acetylcholine (ACh) plays a critical role in cognition, and decreased cholinergic input to the cerebral cortex contributes to the cognitive deficits observed in Alzheimer's disease, dementia with Lewy Bodies, Parkinson's dementia, and other neurological diseases. However, a lack of knowledge regarding the pharmacology of cholinergic effects, or the mechanisms by which ACh influences neuronal activity, have hampered the development of therapies specific to these debilitating diseases. The data that do exist appear conflicting, and have been difficult to reconcile. Indeed, ACh paradoxically generates two opposing responses in the deep-layer pyramidal neurons that provide the majority of cortical output: a fast transient inhibition and a longer-lasting excitation. Although the mechanisms mediating inhibitory cholinergic responses in these neurons (M1-like muscarinic acetylcholine receptor activation, calcium- release from intracellular calcium stores, and subsequent activation of an SK-type calcium-activated potassium conductance) have been well described, the mechanisms mediating cholinergic excitation, and the functional relationship between excitatory and inhibitory cholinergic signaling, remain unknown. This project aims to determine the receptor subtypes, signaling cascades, and ionic mechanisms responsible for cholinergic excitation in cortical layer 5 pyramidal neurons, and to test the overarching hypothesis that excitatory actions of ACh reflect activation of a calcium-permeable non-selective cationic conductance that acts functionally to replenish the intracellular calcium stores that gate inhibitory cholinergic signaling. We propose to use electrophysiological and imaging approaches in a brain slice preparation to address the following three specific aims: 1. To identify the specific muscarinic receptor(s) mediating cholinergic excitation and inhibition in neocortical layer 5 pyramidal neurons. 2. To determine the signaling cascades and ionic mechanism responsible for cholinergic excitation of layer 5 neurons. 3. To test the unifying hypothesis that excitatory cholinergic conductances serve functionally to refill intracellular calcium stores depleted during inhibitory cholinergic signaling. Our results will provide a framework for understanding the biological basis for cholinergic facilitation of cognitive function. This new knowledge will increase our understanding of why dysfunction of cholinergic systems leads to the functional deficits observed in dementia and other disease states, and will provide new targets for therapeutic intervention. The Public Health Relevance: Acetylcholine is a brain chemical necessary for normal cognitive function, and loss of acetylcholine is associated with Alzheimer's disease and other disease states. This project will determine the biological mechanisms by which acetylcholine influences the activity of neurons in the normal cerebral cortex, with the aim of understanding why loss of acetylcholine during aging or disease leads to cognitive dysfunction.