Literature DB >> 19133984

Persistent (current) in the face of adversity ... a new class of cardiac anti-ischaemic compounds on the horizon?

David A Saint1.   

Abstract

Although a persistent component of the sodium current (INaP) was described in cardiac tissue about three decades ago, its physiological role and potential as a therapeutic target was not immediately apparent. Subsequent demonstrations that INaP is enhanced by hypoxia and ischaemia, and that Na+ influx via INaP may contribute to cellular damage, diastolic dysfunction and arrhythmias during ischaemia and reperfusion, raised interest in INaP as a target for anti-ischaemic drugs. Several agents have now been developed to clinical stages, which have INaP block as either their main action, or as a useful co-effect. In this issue of the British Journal of Pharmacology, Vacher et al. report the anti-ischaemic actions of F15845, which appears to exhibit the most selective block of INaP yet described. Its efficacy in animal models of angina raises the prospect of new, specific, INaP blockers that may represent a largely unexploited opportunity for a new class of anti-ischaemic compounds.

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Year:  2009        PMID: 19133984      PMCID: PMC2697828          DOI: 10.1111/j.1476-5381.2008.00077.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  12 in total

Review 1.  Cardiac channelopathies.

Authors:  Eduardo Marbán
Journal:  Nature       Date:  2002-01-10       Impact factor: 49.962

2.  Hypoxia increases persistent sodium current in rat ventricular myocytes.

Authors:  Y K Ju; D A Saint; P W Gage
Journal:  J Physiol       Date:  1996-12-01       Impact factor: 5.182

3.  Contribution of the Na(+) channel and Na(+)/H(+) exchanger to the anoxic rise of [Na(+)] in ventricular myocytes.

Authors:  B N Eigel; R W Hadley
Journal:  Am J Physiol       Date:  1999-11

4.  The rise of [Na(+)] (i) during ischemia and reperfusion in the rat heart-underlying mechanisms.

Authors:  Iwan A Williams; Xiao-hui Xiao; Yue-kun Ju; David G Allen
Journal:  Pflugers Arch       Date:  2007-03-14       Impact factor: 3.657

5.  Role of intracellular Na+ in Ca2+ overload and depressed recovery of ventricular function of reperfused ischemic rat hearts. Possible involvement of H+-Na+ and Na+-Ca2+ exchange.

Authors:  M Tani; J R Neely
Journal:  Circ Res       Date:  1989-10       Impact factor: 17.367

6.  A persistent sodium current in rat ventricular myocytes.

Authors:  D A Saint; Y K Ju; P W Gage
Journal:  J Physiol       Date:  1992       Impact factor: 5.182

7.  RSD1235 blocks late INa and suppresses early afterdepolarizations and torsades de pointes induced by class III agents.

Authors:  Peter M R Orth; J Christian Hesketh; Carmen K H Mak; Yi Yang; Shunping Lin; Gregory N Beatch; Alan M Ezrin; David Fedida
Journal:  Cardiovasc Res       Date:  2006-02-14       Impact factor: 10.787

8.  Effects of lignocaine and quinidine on the persistent sodium current in rat ventricular myocytes.

Authors:  Y K Ju; D A Saint; P W Gage
Journal:  Br J Pharmacol       Date:  1992-10       Impact factor: 8.739

9.  Effect of tetrodotoxin on action potentials of the conducting system in the dog heart.

Authors:  E Coraboeuf; E Deroubaix; A Coulombe
Journal:  Am J Physiol       Date:  1979-04

10.  Electrophysiological effects of ranolazine, a novel antianginal agent with antiarrhythmic properties.

Authors:  Charles Antzelevitch; Luiz Belardinelli; Andrew C Zygmunt; Alexander Burashnikov; José M Di Diego; Jeffrey M Fish; Jonathan M Cordeiro; George Thomas
Journal:  Circulation       Date:  2004-08-09       Impact factor: 29.690

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