Selective muscarinic receptor agonists and antagonists

被引:131
作者
Eglen, RM
Watson, N
机构
[1] ROCHE BIOSCI,INST PHARMACOL,PALO ALTO,CA 94304
[2] LANDESVERSICHERUNGSANSTALT HAMBURG,GROSSHANSDORF HOSP,CTR PNEUMOL & THORAC SURG,D-22927 GROSSHANSDORF,GERMANY
来源
PHARMACOLOGY & TOXICOLOGY | 1996年 / 78卷 / 02期
关键词
D O I
10.1111/j.1600-0773.1996.tb00181.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Muscarinic receptors are composed of a family of four subtypes each of which can be distinguished pharmacologically and structurally. The physiological role of each subtype in the central and peripheral nervous systems remains to be clarified, due, in part, to a lack of agonists and antagonists with adequate subtype selectivity. Nonetheless, several agonists with functional selectivity for M(1) receptors are now in advanced clinical evaluation for Alzheimer's disease, while selective M(1)/M(3) antagonists may prove useful in the treatment of disorders of smooth muscle function. These novel compounds thus provide an advance over earlier therapeutics with which the clinical efficacy was compromised by the side effect profile. This review attempts to assess novel, selective agonists and antagonists, both in terms of their use in defining muscarinic receptor subtypes and their potential clinical utility.
引用
收藏
页码:59 / 68
页数:10
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