Methods for reducing mitochondrial dysfunction
Disclosed are methods and compositions for reducing the epigenetic age of organisms, especially that of adult humans, which provide for proliferating endogenous stem cells, removing aberrant epigenetic marks from chromosomes and mitochondrial DNA, and replacement of senescent cells.
1. A method for reducing methylation of a subject's mitochondrial DNA (mtDNA) in a subject in need thereof, comprising the steps of:
(a) administering to the subject a therapeutically effective amount of a promoter for mitochondrial fission selected from the group consisting of nicotinamide, nicotinic acid, nicotinamide riboside, nicotinamide mononucleotide, oxidized nicotinamide adenine dinucleotide, apigenin, and a combination thereof; and a therapeutically effective amount of a promoter for mitochondrial biogenesis selected from the group consisting of pyrroloquinoline quinone (PQQ), esters, isomers, and derivatives thereof;
(b) allowing a first interval;
(c) administering to the subject a therapeutically effective amount of a promoter for mitochondrial fusion selected from the group consisting of stearic acid or bioavailable source thereof, sulforaphane or bioavailable source thereof, dihydromyricetin, fusion promoter M1 (1-(5-Chloro-2-hydroxyphenyl)-ethanone 2-(2,4,6-trichlorophenyl)hydrazone), and a combination thereof; and a therapeutically effective amount of a promoter for mitochondrial biogenesis selected from the group consisting of pyrroloquinoline quinone (PQQ), esters, isomers, and derivatives thereof;
(d) allowing a second interval; and
(e) cycling steps (a) through (d) a plurality of times.
2. The method as recited in claim 1 , wherein step (a) and/or step (c) further comprise administering to the subject a therapeutically effective amount of a promoter of demethylase.
3. The method as recited in claim 1 , wherein steps (a) and (c) are interchanged.
4. The method as recited in claim 3 , wherein step (a) and/or step (c) further comprise administering to the subject a therapeutically effective amount of a promoter of demethylase.
5. The method as recited in claim 1 , wherein an exercise of counting repetitions (reps) to exhaustion of a muscle group is performed during steps (b) and (d).
6. The method as recited in claim 1 , wherein the promoters of steps (a) and (c) are provided to the subject for self-administration.
7. The method as recited in claim 3 , wherein the promoters of steps (a) and (c) are provided to the subject for self-administration.
8. The method as recited in claim 2 , wherein the promoter of demethylase is selected from the group consisting of alpha-ketoglutarate, alpha-ketoglutaric acid, ammonium alpha-ketoglutarate, arginine alpha-ketoglutarate, calcium alpha-ketoglutarate, creatine alpha-ketoglutarate, glutamine alpha-ketoglutarate, leucine alpha-ketoglutarate, lithium alpha-ketoglutarate, magnesium alpha-ketoglutarate, ornithine alpha-ketoglutarate, potassium alpha-ketoglutarate, sodium alpha-ketoglutarate, taurine alpha-ketoglutarate, and a combination thereof.
9. The method as recited in claim 4 , wherein the promoter of demethylase is selected from the group consisting of alpha-ketoglutarate, alpha-ketoglutaric acid, ammonium alpha-ketoglutarate, arginine alpha-ketoglutarate, calcium alpha-ketoglutarate, creatine alpha-ketoglutarate, glutamine alpha-ketoglutarate, leucine alpha-ketoglutarate, lithium alpha-ketoglutarate, magnesium alpha-ketoglutarate, ornithine alpha-ketoglutarate, potassium alpha-ketoglutarate, sodium alpha-ketoglutarate, taurine alpha-ketoglutarate, and a combination thereof.
10. The method as recited in claim 1 , wherein the first and second intervals are at least one hour.
11. The method as recited in claim 1 , wherein the first and second intervals are at least about one day.