毒扁豆碱
兴奋剂
毒蕈碱乙酰胆碱受体
毒蕈碱乙酰胆碱受体M1
胆碱能的
药理学
毒蕈碱乙酰胆碱受体M4
医学
药效学
毒蕈碱激动剂
胆碱酯酶
部分激动剂
内科学
药代动力学
受体
作者
Richard Lucas,J. Heaton,G. V. Carter,H. Satterwhite
出处
期刊:Advances in behavioral biology
日期:1995-01-01
卷期号:: 469-473
被引量:3
标识
DOI:10.1007/978-1-4757-9145-7_68
摘要
Xanomeline (LY246708/NNC-11-0232) is a potent and selective muscarinic cholinergic M1 receptor agonist which has been shown to cross the blood brain barrier in animals. Increasing central cholinergic activity may provide a rational approach to therapy of Alzheimer's dementia, since physostigmine and other acetyl cholinesterase inhibitors have shown therapeutic promise in such patients. The non-specificity and side-effect profile of this class of drugs is however less than optimal. As the density of post synaptic M1 receptors in the cortex and hippocampus remains largely unchanged in Alzheimer's patients it is predicted that a cerebrally bioavailable and specific muscarinic agonist will have therapeutic utility without undesirable side effects.
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