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Functional Proteins Involved in Regulation of Intracellular Ca2+ for Drug Development:Pharmacology of SEA0400, a Specific Inhibitor of the Na+-Ca2+ Exchanger
[摘要] References(38)Cited-By(12)The Na+-Ca2+ exchanger (NCX) is involved in regulation of intracellular Ca2+ concentration. A specific inhibitor of NCX has been required for clarification of the physiological and pathological roles of NCX. We have developed 2-[4-[(2,5-difluorophenyl)methoxy]phenoxy]-5-ethoxyaniline (SEA0400), a highly potent and selective inhibitor of NCX. SEA0400 in the concentration range that inhibits NCX exhibits negligible affinities for the Ca2+ channels, Na+ channels, K+ channels, noradrenaline transporter, and 14 receptors; and it does not affect the activities of the store-operated Ca2+ channel, Na+-H+ exchanger, and several enzymes including Na+,K+-ATPase and Ca2+-ATPase. Furthermore, recent studies show that SEA0400 attenuates ischemia-reperfusion injury in the brain, heart, and kidney and radiofrequency lesion-induced edema in rat brain. These findings suggest that NCX plays a key role in ischemia-reperfusion injury and may be a target molecule for treatment of reperfusion injury-related diseases.
[发布日期]  [发布机构] 
[效力级别]  [学科分类] 药学
[关键词] Na+-Ca2+ exchanger;SEA0400;edema;ischemia/reperfusion injury;apoptosis [时效性] 
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