Woodruff-Pak Diana S, Lander Cynthia, Geerts Hugo
Albert Einstein Healthcare Network, Korman Suite 100, 5501 Old York Road, Philadelphia, PA 19141, USA.
CNS Drug Rev. 2002 Winter;8(4):405-26. doi: 10.1111/j.1527-3458.2002.tb00237.x.
Nicotinic acetylcholine receptor pharmacology is becoming increasingly important in the clinical symptomatology of neurodegenerative diseases in general and of cognitive and behavioral aspects in particular. In addition, the concept of allosteric modulation of nicotinic acetylcholine receptors has become a research focus for the development of therapeutic agents. In this review the scientific evidence for changes in nicotinic acetylcholine receptors in Alzheimer's disease is described. Within this context, the pharmacology of galantamine, a recently approved drug for cognition enhancement in Alzheimer's disease, is reviewed along with preclinical studies of its efficacy on learning and memory. Galantamine modestly inhibits acetylcholinesterase and has an allosteric potentiating ligand effect at nicotinic receptors. The data collected in this review suggest that the unique combination of acetylcholinesterase inhibition and nicotinic acetylcholine receptor modulation offers potentially significant benefits over acetylcholinesterase inhibition alone in facilitating acetylcholine neurotransmission.
一般而言,烟碱型乙酰胆碱受体药理学在神经退行性疾病的临床症状学中愈发重要,尤其在认知和行为方面。此外,烟碱型乙酰胆碱受体的变构调节概念已成为治疗药物开发的研究重点。在这篇综述中,描述了阿尔茨海默病中烟碱型乙酰胆碱受体变化的科学证据。在此背景下,对加兰他敏(一种最近被批准用于增强阿尔茨海默病认知功能的药物)的药理学以及其对学习和记忆功效的临床前研究进行了综述。加兰他敏可适度抑制乙酰胆碱酯酶,并对烟碱型受体具有变构增强配体效应。本综述收集的数据表明,与单独抑制乙酰胆碱酯酶相比,抑制乙酰胆碱酯酶和调节烟碱型乙酰胆碱受体的独特组合在促进乙酰胆碱神经传递方面可能具有显著益处。