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Inhibition of late sodium current to reduce electrical and mechanical dysfunction of ischaemic myocardium
Author(s) -
Shryock J C,
Belardinelli L
Publication year - 2008
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0707522
Subject(s) - ranolazine , medicine , ischemia , ischaemic heart disease , clinical trial , cardiology , drug , pharmacology
This commentary on the review by DA Saint in the current issue of the British Journal of Pharmacology focuses on the pathological role of late I Na in the heart, the evidence supporting inhibition of late I Na as a therapeutic target in ischaemic heart disease, and the therapeutic applications and challenges for development of new late I Na inhibitors. Recent reports from a large clinical outcome trial (MERLIN) of ranolazine, a drug known to inhibit late I Na , indicated that it was safe and reduced recurrent ischaemia and arrhythmic activity. In combination with other results indicating that inhibition of late I Na reduces ischaemia, myocardial Ca 2+ overload, and electrical and mechanical dysfunction when late I Na is increased, the new clinical trial results suggest that reduction of cardiac late I Na is safe and therapeutically beneficial. British Journal of Pharmacology (2008) 153 , 1128–1132; doi: 10.1038/sj.bjp.0707522 ; published online 10 December 2007
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