KATP channel pharmacogenomics:: From bench to bedside

被引:34
作者
Sattiraju, S. [1 ,2 ]
Reyes, S. [1 ,2 ]
Kane, G. C. [1 ,2 ]
Terzic, A. [1 ,1 ,2 ]
机构
[1] Mayo Clin, Dept Med Genet, Rochester, MN USA
[2] Mayo Clin, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN USA
关键词
D O I
10.1038/sj.clpt.6100378
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inheritance plays a significant role in defining drug response and toxicity. Advances in molecular pharmacology and modern genomics emphasize genetic variation in dictating inter-individual pharmacokinetics and pharmacodynamics. A case in point is the homeostatic ATP-sensitive potassium (K-ATP) channel, an established drug target that adjusts membrane excitability to match cellular energetic demand. There is an increased recognition that genetic variability of the K-ATP channel impacts therapeutic decisionmaking in human disease.
引用
收藏
页码:354 / 357
页数:4
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