Compositions and methods for treating or preventing atrial fibrillation
The present invention provides compositions and methods for treating or preventing atrial fibrillation (AF). In particular, the present invention provides administration of muscarinic receptor antagonists (e.g., M2-selective muscarinic receptor blockers), administered alone or in combination with other therapeutic agents (e.g., beta-adrenergic receptor blockers) to treat and/or prevent atrial fibrillation.
1. A method of treating, reversing, and/or preventing cardiac arrhythmia in a human subject comprising co-administering a therapeutically effective amount of a beta-adrenergic receptor blocking agent and a therapeutically effective amount of a muscarinic receptor blocking agent directly to the surface of the heart of said human subject.
2. The method of claim 1 , wherein said beta-adrenergic receptor blocking agent is selected from the group consisting of aprenolol, carteolol, levobunolol, mepindolol, metipranolol, nadolol, oxprenolol, timolol, sotalol, esmolol, cateolol, propranolol, betaxolol, penbutolol, metoprolol, acebutolol, atenolol, metoprolol, pindolol, bisoprolol, nebivolol, amosulalol, landiolol, and tilisolol, including any salts, hydrates, solvates, prodrugs, and any crystal forms in which they may occur.
3. The method of claim 1 , wherein said muscarinic receptor blocker is selected from the group comprising atropine, scopolamine, ipratropium, tropicamide, pirenzepine, diphenhydramine, dimenhydrinate, dicyclomine, oxybutynin, tiotropium, cyclopentolate, atropine methonitrate, trihexyphenidyl, tolterodine, solifenacin, darifenacin, benzatropine, and mebeverine, including any salts, hydrates, solvates, prodrugs, and any crystal forms in which they may occur.
4. The method of claim 1 , wherein said muscarinic receptor blocker is a M2-selective muscarinic receptor subtype.
5. The method of claim 1 , wherein said cardiac arrhythmia comprises atrial fibrillation.
6. The method of claim 1 , wherein said beta-adrenergic receptor blocking agent is not esmolol.
7. A method of treating, reversing, and/or preventing cardiac arrhythmia in a human subject comprising administering a therapeutically effective amount of an M2-selective muscarinic receptor blocking agent directly to the surface of the heart of said human subject.
8. The method of claim 7 , wherein the cardiac arrhythmia is atrial fibrillation.
9. The method of claim 7 , wherein said M2-selective muscarinic receptor blocking agent selectively blocks the M2 receptor subtype by at least five-fold versus the M3 receptor subtype.
10. The method of claim 9 , wherein said M2-selective muscarinic receptor blocking agent selectively blocks the M2 receptor subtype by at least five-fold versus the M1 receptor subtype.
11. The method of claim 7 , wherein said M2-selective muscarinic receptor blocking agent is selected from Sch 211803, TD-6301, and methoctramine.
12. The method of claim 1 , wherein said beta-adrenergic receptor blocking agent is propranolol.
13. The method of claim 12 , wherein said muscarinic receptor blocking agent is atropine.
14. A method of treating, reversing, and/or preventing cardiac arrhythmia in a human subject comprising co-administering directly to the surface of the heart of said human subject a therapeutically effective amount of a beta-adrenergic receptor blocking agent and a therapeutically effective amount of a muscarinic receptor blocking agent, wherein said beta-adrenergic receptor blocking agent is selected from the group consisting of esmolol aprenolol, carteolol, levobunolol, mepindolol, metipranolol, nadolol, oxprenolol, timolol, sotalol, cateolol, propranolol, betaxolol, penbutolol, metoprolol, acebutolol, atenolol, metoprolol, pindolol, bisoprolol, nebivolol, amosulalol, landiolol, and tilisolol, including any salts, hydrates, solvates, prodrugs, and any crystal forms in which they may occur.