Kamkwalala Asante R, Newhouse Paul A
Center for Cognitive Medicine, Department of Psychiatry, Vanderbilt University, Nashville, TN 37212, United States.
Center for Cognitive Medicine, Department of Psychiatry, Vanderbilt University, 1601 23rd Ave S Suite 3080 Nashville TN 37212, United States.
Curr Alzheimer Res. 2017;14(4):377-392. doi: 10.2174/1567205013666160930112625.
The major components of the cholinergic receptor system of the human brain include projections from the basal forebrain nuclei, and utilize the two types of receptors that they synapse on, nicotinic and muscarinic acetylcholine receptors. With the widespread cortical and subcortical projections of the basal forebrain, activity of these two receptor systems provide modulation of neurotransmitter activity underlying normal cognitive processes, such as attention, episodic memory, and working memory. Alzheimer's disease (AD) targets and damages cholinergic neurons in the basal forebrain, and as these projections are lost, cognitive performance progressively declines. Currently, the most widely prescribed treatment for AD is acetylcholinesterase inhibitor medications, which work by partially blocking the degradation of acetylcholine in the synapse and enabling more of the neurotransmitter to reach and activate cholinergic receptors. However since these medications have limited effectiveness, alternate treatments that focus on augmenting the activity of the receptors themselves, independent of acetylcholinesterase inhibition, are being explored. This review will discuss: 1) the role of the cholinergic system in modulating cognition, 2) novel cholinergic treatment strategies for AD-related cognitive decline, in particular treatments intended to increase cholinergic system activity by selectively targeting muscarinic and nicotinic acetylcholinergic receptors to improve cognitive performance, 3) risks, and additional considerations for cholinergic cognitive treatments for AD.
人类大脑胆碱能受体系统的主要组成部分包括来自基底前脑核的投射,并利用它们所突触的两种受体,即烟碱型和毒蕈碱型乙酰胆碱受体。随着基底前脑广泛的皮质和皮质下投射,这两种受体系统的活动对正常认知过程(如注意力、情景记忆和工作记忆)背后的神经递质活动起到调节作用。阿尔茨海默病(AD)靶向并损害基底前脑的胆碱能神经元,随着这些投射的丧失,认知能力逐渐下降。目前,治疗AD最广泛使用的药物是乙酰胆碱酯酶抑制剂,其作用机制是部分阻断突触中乙酰胆碱的降解,使更多的神经递质能够到达并激活胆碱能受体。然而,由于这些药物的有效性有限,人们正在探索其他专注于增强受体自身活性(独立于乙酰胆碱酯酶抑制作用)的治疗方法。本综述将讨论:1)胆碱能系统在调节认知中的作用;2)针对AD相关认知衰退的新型胆碱能治疗策略,特别是旨在通过选择性靶向毒蕈碱型和烟碱型乙酰胆碱受体来增加胆碱能系统活性以改善认知表现的治疗方法;3)AD胆碱能认知治疗的风险及其他注意事项。