Anti-arrhythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) and uses thereof
View Patent ↗The present invention provides methods for limiting or preventing a decrease in the level of RyR2-bound FKBP12.6 in a subject. The present invention further provides methods for treating and preventing atrial and ventricular cardiac arrhythmias, heart failure, and exercise-induced sudden cardiac death in a subject. Additionally, the present invention provides use of JTV-519 in a method for limiting or preventing a decrease in the level of RyR2-bound FKBP12.6 in a subject who has, or is a candidate for, atrial fibrillation. Also provided are uses of 1,4-benzothiazepine derivatives in methods for treating and preventing atrial and ventricular cardiac arrhythmias and heart failure in a subject, and for preventing exercise-induced sudden cardiac death. The present invention also provides methods for identifying agents for use in treating and preventing atrial fibrillation and heart failure, and agents identified by these methods.
1. A method for increasing binding of FKBP12.6 to RyR2 in a subject, or limiting a decrease in the level of RyR2-bound FKBP12.6 in a subject, comprising administering an effective amount of an agent to the subject, wherein the agent has the formula:
wherein
R 1 =OR′ at position 7 on the benzothiazepine ring;
R′=alkyl;
R 2 =H;
R 3 =H;
R 4 =halide, carboxylic acid, or an alkyl-O— or —S-alkyl-S—; and
m=0, 1, or 2.
2. The method of claim 1 , wherein the subject is a human.
3. The method of claim 1 , wherein the subject has a cardiac condition selected from the group consisting of cardiac arrhythmia, tachycardia, ventricular arrhythmia, ventricular fibrillation, ventricular tachycardia, sustained ventricular tachycardia, non-sustained ventricular tachycardia, catecholaminergic polymorphic ventricular tachycardia (CPVT), heart failure, sudden cardiac death and exercise-induced sudden cardiac death.
4. The method of claim 1 , wherein the effective amount of the agent is one or more of:
(a) from about 5 mg/kg/day to about 20 mg/kg/day,
(b) an amount resulting in a plasma concentration of from about 0.02 μM to about 1 μM in the subject, or
(c) an amount resulting in a plasma concentration of from about 300 ng/ml to about 1000 ng/ml in the subject.
5. The method of claim 1 , wherein the agent is
6. A method for reducing the risk of sudden cardiac death, sustained ventricular tachycardia and non-sustained ventricular tachycardia in a subject, comprising administering an effective amount of an agent to the subject, wherein the agent has the formula:
wherein
R 1 =OR′ at position 7 on the benzothiazepine ring;
R′ =alkyl;
R 2 =H;
R 3 =H;
R 4 =halide, carboxylic acid, or an alkyl-O— or —S-alkyl-S—; and
m=0, 1, or 2.
7. The method of claim 6 , wherein the agent is administered to a subject that has or is at risk of developing a condition selected from the group consisting of cardiac arrhythmia, tachycardia, ventricular arrhythmia, ventricular fibrillation, ventricular tachycardia, sustained ventricular tachycardia, non-sustained ventricular tachycardia, catecholaminergic polymorphic ventricular tachycardia (CPVT), heart failure, sudden cardiac death and exercise-induced sudden cardiac death.
8. The method of claim 6 , wherein the effective amount of the agent is one or more of:
(a) from about 5 mg/kg/day to about 20 mg/kg/day,
(b) an amount resulting in a plasma concentration of from about 0.02 μM to about 1.0 μM in the subject, or
(c) an amount resulting in a plasma concentration of from about 300 ng/ml to about 1000 ng/ml in the subject.
9. The method of claim 6 , wherein the agent is
10. The method of claim 6 , wherein the subject is a human.
11. The method of claim 1 , wherein R 4 =carboxylic acid and m=0 or 1.
12. The method of claim 1 , wherein m=0 or 1.
13. The method of claim 12 , wherein R 4 =carboxylic acid and R′=methyl.
14. The method of claim 13 , wherein m=0; and R 4 =carboxylic acid.
15. The method of claim 6 , wherein R 4 =carboxylic acid and m=0 or 1.
16. The method of claim 6 , wherein m=0 or 1.
17. The method of claim 16 , wherein R 4 =carboxylic acid and R′=methyl.
18. The method of claim 17 , wherein m=0; and R 4 =carboxylic acid.
19. A method for treating cardiac arrhythmia in a subject, comprising administering an effective amount of an agent to the subject, wherein the agent has the formula:
wherein
R 1 =OR′ at position 7 on the benzothiazepine ring;
R′ =alkyl;
R 2 =H;
R 3 =H;
R 4 =halide, carboxylic acid, or an alkyl-O— or —S-alkyl-S—; and
m=0, 1, or 2.
20. The method of claim 19 , wherein the effective amount of the agent is one or more of:
(a) from about 5 mg/kg/day to about 20 mg/kg/day,
(b) an amount resulting in a plasma concentration of from about 0.02 μM to about 1 μM in the subject, or
(c) an amount resulting in a plasma concentration of from about 300 ng/ml to about 1000 ng/ml in the subject.
21. The method of claim 19 , wherein the agent is
22. The method of claim 19 , wherein the subject is a human.
23. The method of claim 19 , wherein R 4 =carboxylic acid and m=0 or 1.
24. The method of claim 19 , wherein m=0 or 1.
25. The method of claim 24 , wherein R 4 =carboxylic acid and R′=methyl.
26. The method of claim 25 , wherein m=0; and R 4 =carboxylic acid.
27. The method of claim 5 , wherein the subject is a human.
28. The method of claim 5 , wherein the subject has a cardiac condition selected from the group consisting of cardiac arrhythmia, tachycardia, ventricular arrhythmia, ventricular fibrillation, ventricular tachycardia, sustained ventricular tachycardia, non-sustained ventricular tachycardia, catecholaminergic polymorphic ventricular tachycardia (CPVT), heart failure, sudden cardiac death and exercise-induced sudden cardiac death.
29. The method of claim 5 , wherein the effective amount of the agent is one or more of:
(a) from about 5 mg/kg/day to about 20 mg/kg/day,
(b) an amount resulting in a plasma concentration of from about 0.02 μM to about 1.0 μM in the subject, or
(c) an amount resulting in a plasma concentration of from about 300 ng/ml to about 1000 ng/ml in the subject.