中枢神经系统疾病中的尼古丁系统:退行性疾病及其他

Paul A Newhouse, Megan Kelton
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引用次数: 79

摘要

对中枢神经系统(CNS)烟碱受体的结构、功能和分布的了解的进展,为研究这些受体及其相关过程在中枢神经系统功能中可能发挥的作用提供了新的推动力。进一步的动机来自于认识到这些受体在退行性神经系统疾病如阿尔茨海默病(AD)和帕金森病(PD)中发生改变。对中枢神经系统烟碱受体分子亚结构及其药理学的持续研究已经开始为烟碱药物治疗中枢神经系统开辟新的可能性。利用这些可能性需要了解这些受体系统在人类认知、行为、运动和感觉功能中所起的作用。对人类认知和行为的仔细研究的线索开始出现,并将为潜在治疗性新型尼古丁制剂的研究提供方向。这些受体的调节与产生治疗效益的最终目标是这些研究和药物开发的目标。本文将回顾我们实验室的研究以及其他指出中枢神经系统尼古丁机制在正常人类认知和行为功能中的重要性以及它们在疾病状态中的作用的研究。此外,本文将研究尼古丁和/或尼古丁激动剂在各种中枢神经系统疾病中的潜在临床应用,特别强调结构性脑疾病,包括:运动障碍,如帕金森病和妥瑞氏综合征,认知/行为障碍,如阿尔茨海默病,注意缺陷/多动障碍,和精神分裂症,以及其他更多的推测应用。在这些疾病状态中提出了尼古丁和/或尼古丁激动剂的早期治疗研究的重要结果。例如,我们小组最近对尼古丁和新型尼古丁激动剂(如ABT-418)在AD患者中的研究表明,尼古丁刺激可以改善口头信息的获取和保留,并减少错误。一系列关于尼古丁对帕金森病患者认知和运动功能的急性和亚慢性定量影响的研究的初步结果表明,急性尼古丁给药和刺激可以改善认知和运动功能的某些方面,并可能提高更复杂任务的处理速度。新型尼古丁激动剂在中枢神经系统疾病中最有可能的近期应用可能是那些本质上退行性疾病,如帕金森病和阿尔茨海默病,或其他运动障碍,如妥瑞氏综合征。除疾病早期或作为预防或预防性治疗外,尼古丁激动剂最可能的直接治疗作用是与其他药物联合作为增强治疗,而不是作为单一治疗。
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Nicotinic systems in central nervous systems disease: degenerative disorders and beyond

Advances in the understanding of the structure, function, and distribution of central nervous system (CNS) nicotinic receptors has provided the impetus for new studies examining the role(s) that these receptors and associated processes may play in CNS functions. Further motivation has come from the realization that such receptors are changed in degenerative neurologic diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD). Ongoing investigations of the molecular substructure of CNS nicotinic receptors and their pharmacology have begun to open up new possibilities for novel CNS therapeutics with nicotinic agents. Exploiting these possibilities will require understanding of the role(s) that these receptor systems play in human cognitive, behavioral, motor, and sensory functioning. Clues from careful studies of human cognition and behavior are beginning to emerge and will provide direction for studies of potentially therapeutic novel nicotinic agents. Modulation of these receptors with the ultimate goal of producing therapeutic benefits is the goal of these investigations and drug development. This paper will review studies from our laboratory and others that point to the importance of CNS nicotinic mechanisms in normal human cognitive and behavioral functioning as well as their role in disease states. In addition, this paper will examine potential clinical applications of nicotine and/or nicotinic agonists in a variety of CNS disorders with particular emphasis on structural brain disease including: movement disorders such as Parkinson's disease and Tourette's syndrome, cognitive/behavioral disorders such as Alzheimer's disease, attention deficit/hyperactivity disorder, and schizophrenia, and other more speculative applications. Important results from early therapeutic studies of nicotine and/or nicotinic agonists in these disease states are presented. For example, recent studies with nicotine and novel nicotinic agonists such as ABT-418 by our group in AD patients suggest that nicotinic stimulation can improve the acquisition and retention of verbal information and decrease errors. Preliminary results from a series of studies examining the acute and subchronic quantitative effects of nicotine on cognitive and motor functioning in Parkinson's disease suggest that acute nicotine administration and stimulation improves some aspects of cognitive and motor performance and may improve the processing speed of more complex tasks. The most likely near-term applications of novel nicotinic agonists in CNS disorders are likely to be in those disorders that are degenerative in nature, e.g. Parkinson's disease and Alzheimer's disease, or other movement disorders such as Tourette's syndrome. The most likely direct therapeutic role for nicotinic agonists is as augmentation therapy in combination with other agents rather than as monotherapy, except early in disease states or as a prophylactic or preventative treatment.

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