I'm beginning to think that even supplementing NADH wouldn be a bad idea. However, I am interested in naturally upping the NAD/NADH ratio instead of just adding more NADH.
http://www.longecity...-nadnadh-ratio/Let me know what you all think!
This is also interesting:
http://www.longecity...-nadnadh-ratio/[reference='']There is also the possibility that aspartic acid will increase the NAD/NADH ratio: trans-aminization will convert aspartic acid to oxolacetic acid, and it is more stable than the later. This has not been tested in vivo, but some Krebs Cycle charts do show the two as acting at the same point in the cycle.
Another amino acid that has been found to increase the NAD ratio is l-serine. I found this claim in a patent search, where the effect was claimed to be found only when l-serine was combine with caffeine. If it does indeed inrease the NAD/NADH ratio, it acts at a different point in the KREBS cycle involving alcohol-dehydrogense. The patent was for a method to speed the metabolization of alcohol and prevent ill effects from alcohol by speeding its metabolization.. The suggested dose was 2 grams of l-serine with 200 mg of caffeine. It was claimed to prevent "Asian Flush" and I believe is intended to be marketed to Japanese men so they can drink more.
Methylene blue oxidizes NADH into NAD*, and increases the NAD/NADH ratio.** However , the effect on longevity was seen at very low concentrations, and the human dose that have been suggested range from 60 mcg (micro-grams) to one drop of a 2% solution. There is a thread on this
http://www.imminst.o...=methylene blue .
So far, in Spindler's longevity test on mice, he mentioned in a talk that he is seeing good results from oxolacetic acid.
*Appl Environ Microbiol. 1985 December; 50(6): 1368-1374
Effect of reducing-equivalent disposal and NADH/NAD on deamination of amino acids by intact rumen microorganisms and their cell extracts.
T Hino and J B Russell
**FASEB J. 2008 Mar;22(3):703-12. Epub 2007 Oct 10.
Methylene blue delays cellular senescence and enhances key
mitochondrial biochemical pathways.
Atamna H, Nguyen A, Schultz C, Boyle K, Newberry J, Kato H, Ames BN[/reference]