Activation of human ClC-2Cl- channels:: Implications for cystic fibrosis

被引:10
作者
Cuppoletti, J [1 ]
Tewari, KP [1 ]
Sherry, AM [1 ]
Malinowska, DH [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Cellular & Mol Physiol, Cincinnati, OH 45267 USA
关键词
acid-activated ion channels; amidation; arachidonic acid; ClC-2Cl(-) channels; cystic fibrosis; omeprazole;
D O I
10.1046/j.1440-1681.2000.03357.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The ClC-2 Cl- channels are present in the adult human lung epithelia and, therefore, are a potential target for therapy in cystic fibrosis. 2. Activators of ClC-2 Cl- channels that may have physiological relevance include activation by reduced external pH, protein kinase A and arachidonic acid. 3. Activators of ClC-2 Cl- channels that have therapeutic potential include amidation and omeprazole and, perhaps, effectors of arachidonic acid metabolism.
引用
收藏
页码:896 / 900
页数:5
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