Pharmacology and physiology of human adrenergic receptor polymorphisms

被引:241
作者
Small, KM [1 ]
McGraw, DW [1 ]
Liggett, SB [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Med, Cincinnati, OH 45267 USA
关键词
G-protein; mutation; pharmacogenetics; genome; sequencing;
D O I
10.1146/annurev.pharmtox.43.100901.135823
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Adrenergic receptors are expressed on virtually every cell type in the body and are the receptors for epinephrine and norepinephrine within the sympathetic nervous system. They serve critical roles in maintaining homeostasis in normal physiologic settings as well as pathologic states. These receptors are also targets for therapeutically administered agonists and antagonists. Recent studies have shown that at least seven adrenergic receptor subtypes display variation in amino acid sequence in the human population due to common genetic polymorphisms. Variations in potential regulatory domains in noncoding sequence are also present. Here, we review the consequences of these polymorphisms in terms of signaling, human physiology and disease, and response to therapy.
引用
收藏
页码:381 / 411
页数:31
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