Literature DB >> 1356284

Block and modulation of cardiac Na+ channels by antiarrhythmic drugs, neurotransmitters and hormones.

A O Grant1, D J Wendt.   

Abstract

The Na+ channel is an important target for the action of antiarrhythmic drugs. Application of contemporary biophysical, biochemical and molecular biological techniques have added considerably to our knowledge of its structure, function, modulation and block by antiarrhythmic drugs. The increased mortality from the use of these drugs for prophylaxis of cardiac arrhythmias has forced a re-evaluation of their use and of the entire pharmacological strategy of arrhythmia management. Gus Grant and David Wendt review recent studies on the block and modulation of cardiac Na+ channels and the place of Na+ channel blockers in future antiarrhythmic drug development.

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Year:  1992        PMID: 1356284     DOI: 10.1016/0165-6147(92)90108-i

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  8 in total

1.  Protein kinase A activation increases sodium current magnitude in the electric organ of Sternopygus.

Authors:  L McAnelly; H H Zakon
Journal:  J Neurosci       Date:  1996-07-15       Impact factor: 6.167

2.  Electromechanical and atrial and ventricular antiarrhythmic actions of CIJ-3-2F, a novel benzyl-furoquinoline vasodilator in rat heart.

Authors:  Gwo-Jyh Chang; Yung-Hsin Yeh; Tsung-Pin Lin; Chi-Jen Chang; Wei-Jan Chen
Journal:  Br J Pharmacol       Date:  2014-08       Impact factor: 8.739

3.  Activation of protein kinase C alters the intracellular distribution and mobility of cardiac Na+ channels.

Authors:  Haifa Hallaq; Dao W Wang; Jennifer D Kunic; Alfred L George; K Sam Wells; Katherine T Murray
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-11-18       Impact factor: 4.733

4.  Electrophysiological basis for antiarrhythmic efficacy, positive inotropy and low proarrhythmic potential of (-)-caryachine.

Authors:  M H Wu; M J Su; S S Lee; L T Lin; M L Young
Journal:  Br J Pharmacol       Date:  1995-12       Impact factor: 8.739

5.  Ionic mechanisms of pacemaker activity in spontaneously contracting atrial HL-1 cells.

Authors:  Zhenjiang Yang; Katherine T Murray
Journal:  J Cardiovasc Pharmacol       Date:  2011-01       Impact factor: 3.105

6.  Cardiac electrophysiologic and antiarrhythmic actions of a pavine alkaloid derivative, O-methyl-neocaryachine, in rat heart.

Authors:  Gwo-Jyh Chang; Ming-Jai Su; Li-Man Hung; Shoei-Sheng Lee
Journal:  Br J Pharmacol       Date:  2002-06       Impact factor: 8.739

7.  Block of voltage-dependent sodium currents by the substance P receptor antagonist (+/-)-CP-96,345 in neurones cultured from rat cortex.

Authors:  M Caeser; G R Seabrook; J A Kemp
Journal:  Br J Pharmacol       Date:  1993-08       Impact factor: 8.739

8.  Increased hindrance on the chiral carbon atom of mexiletine enhances the block of rat skeletal muscle Na+ channels in a model of myotonia induced by ATX.

Authors:  J F Desaphy; D Conte Camerino; C Franchini; G Lentini; V Tortorella; A De Luca
Journal:  Br J Pharmacol       Date:  1999-11       Impact factor: 8.739

  8 in total

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