Modulation of sodium channels by nicotinamide adenine dinucleotide
View Patent ↗The present invention relates to the use of oxidized nicotinamide adenine dinucleotide (NAD + ) or of its reduced form, NADH, as sodium channel modulators. The present invention also relates to the use of compositions containing NAD + or NADH to treat conditions associated with sodium channel current, such as arrhythmia. NAD + is found to increase sodium channel current, while NADH is found to decrease sodium channel current. Thus, conditions that are associated with decreased sodium channel current can be treated with NAD + , while conditions that is associated with increased sodium channel current can be treated with NADH.
1. A method for modulating or for controlling sodium channel current of a cell having an altered sodium current, comprising the step of contacting the cell with a composition containing NAD + to increase the sodium current or with a composition containing NADH to decrease the sodium current.
2. The method of claim 1 , wherein the cell expresses sodium channels.
3. The method of claim 1 , wherein the cell expresses SCN5A.
4. The method of claim 1 , wherein the NAD + or NADH concentration is about 100-300 μM.
5. A method for reducing arrhythmic risk associated with an altered sodium current comprising the step of administering a composition containing NAD+ to an individual in need thereof.
6. The method of claim 5 , wherein the amount of NAD + is effective to reduce arrhythmic risk.
7. The method of claim 5 , wherein the amount of NAD + is effective to achieve a NAD + blood concentration of about 100-300 μM.
8. The method of claim 5 , wherein the individual is suffering from arrhythmia.
9. The method of claim 5 , wherein the administering step comprises intravenous administration of the composition.
10. The method of claim 5 , wherein the composition is selected from the group consisting of a powder, a tablet, a capsule, a solution, and a suspension.
11. The method of claim 5 , wherein the NAD + or NADH is about 0.1 to about 90% by weight of the composition.
12. The method of claim 5 , wherein the composition is a solution for intravenous administration.