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Kevin A. Negrete - President

Kevin A. Negrete - President. DNA Workshop (Bologna, Italy). To live better …. longer. To increase the quality of life after 40. Two main factors contributing longer (historical) lifespan. Two main factors contributing to limited lifespan. reduce cellular oxidation .

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Kevin A. Negrete - President

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  1. Kevin A. Negrete - President

  2. DNA Workshop(Bologna, Italy)

  3. To live better… longer To increase the quality of life after 40

  4. Two main factors contributing longer (historical) lifespan

  5. Two main factors contributing to limited lifespan

  6. reduce cellular oxidation the formation of nascent oxygen (O2) and the elimination of free radicals (O+)

  7. Two main factors contributing to limited lifespan X ? or is it? X ?

  8. Research has allowed scientists to identify central aging system in cells – and specifically the aging clock in DNA The two basic DNA markers that regulate aging are Telomere length and Methyl Group Loss

  9. Telomere Inside the center or nucleus of a cell, our genes are located on twisted, double-stranded molecules of DNA called chromosomes. At the ends of the chromosomes are stretches of DNA called telomeres, which protect our genetic data, make it possible for cells to divide. Telomeres have been compared with the plastic tips on shoelaces because they prevent chromosome ends from fraying and sticking to each other, which would scramble an organism's genetic information to cause cancer, other degenerative diseases, or death. Each time a cell divides the telomeres get shorter (by 30-200 BP). Healthy cells only divide between 50-70 times. When telomeres get too short, the cells no longer can divide and becomes inactive, sustain genetic damage and ultimately die.

  10. Similar to telomere shortening – the loss of Methyl Groups (CH3) shows a specific preprogrammed degradation throughout mammalian lifespan. The degradation is accelerated by oxidative stress, poor nutrition, lack of exercise, and environmental toxins. H H H H H H H H H

  11. Final Common Pathway of Aging – DNA Demethylation 10% loss 25 yrs 20% loss 50 yrs 30% loss 75 yrs 40% loss Death Birth

  12. Understand true anti-aging (DNA) mammalian chemistry consists of 2 goals: elongate telomers and increase DNA methylation. ENHANCED NUCLEOTIDE SUPPLEMENATION

  13. Longevity of Control vs. Treated Animals 2500 2000 1500 1500 1000 750 150 750 750 Control Treated

  14. Record mammalian longevity achieved through weekly injection of DNA and RNA • Study began with 750 day old rats with usual longevity of 800 to 900 days • Identical conditions except treated animals received nucleic acid injections • Post 8 weeks control rats lost fur and vitality, whereas treated animals increased muscle mass, libido, and activity levels • Control animals all died in less than 150 days from start of study • Treated animals lived a minimum of 850 up to 1500 additional days from start of study, doubling and even tripling the usual life span

  15. Understand true anti-aging (DNA) mammalian chemistry consists of 2 goals: elongate telomers and increase DNA methylation. HOMOCYSTEINE

  16. What is Homocysteine? Homocysteine is a toxic amino acid by-product produced by our own organism and accumulates in the bloodstream. Elevated homocysteine is not only the indicator of, but is the CAUSE of many major diseases includinAlzheimer’, Arthritis, Cancer, Chronic Fatigue, Depression, Diabetes, Heart Attacks, Infertility, Obesity, Strokes, Thyroid Problems, and Ulcers Homocysteine also accelerates the oxidation of LDL

  17. Homocysteine Level VS Cardiac Risk Ratio

  18. Research has shown that higher HOMOCYSTEINE levels are directly related to demethylation and telomere shortening 3 ways to detoxify HOMOCYSTEINE

  19. Methyl Group Transfer Metabolic Pathways Methionine ATP S-adenosyl-methionine (SAMe) DMG B12 Folic Acid Betaine (TMG) Donates CH3 to: DNA Proteins Lipids Carbohydrates Myelin Detox Pathways Neurotransmitter Production And others S-adenosyl-homocysteine (SAH) Choline Homocysteine (Hcy) Zn Vitamin B6 Cysteine Glutathione

  20. We have developed THE ENGINE OF REMETHYLATION making cells younger through Enhanced Nucleotide Supplementation

  21. Methyl Group Transfer Metabolic Pathways Methionine ATP S-adenosyl-methionine (SAMe) DMG B12 Folic Acid Betaine (TMG) Donates CH3 to: DNA Proteins Lipids Carbohydrates Myelin Detox Pathways Neurotransmitter Production And others S-adenosyl-homocysteine (SAH) Choline Homocysteine (Hcy) Zn Vitamin B6 Cysteine Glutathione

  22. Could life-extension and anti-aging be as simple as supplying the body with DNA and RNA?

  23. Primary source of nucleotides is endogenous synthesis from amino acids and simple precursors • Therefore nucleic acids have generally been considered nonessential nutrients • Under stress, however, some tissues unable to produce enough nucleotides to support tissue needs • In these conditions, nucleic acids bases may become essential nutrients for optimum tissue repair and function • Glycine, Serine, Aspartic Acid, Glutamine

  24. Nucleic Acids : Food & Supplementation

  25. So why doesn’t everyone just take a giant nucleic acid pill?

  26. Orally ingested nucleic acids undergo intensive metabolic degradation in upper GI tract • Over 99% of purine bases oxidized to uric acid before entering portal circulation • About 95% of pyrimidines are metabolized before leaving intestinal lining • Only 3% of ingested pyrimidines reach liver

  27. Photo Acoustic Resonance Laser

  28. Laser Enhancement Technology Nutrient molecules get distorted during food or supplementation processing. Result: reduced nutrient assimilation by the cells. Laser Enhancement Technology reshapes nutrient molecules. Result: increased nutrient assimilation by the cells.

  29. Laser Homogenized Betaine HCl Crystal Control Betaine HCl

  30. Extensive experimental and clinical evidence for benefit from nucleotide supplementation • Increased survival in mice with Staph aureus bacteremia from 21% to 71% • Significantly increased survival in mice with Candida sepsis – greater effect with parenteral nucleotides than oral administration • Survival in animals with high dose radiation exposure increased from 5% to 50%

  31. Single injection of RNA in mice post tumor immunization improved outcome from 0% to 40% long term survival • Rate of liver regeneration in rats post 70% hepatectomy significantly greater if IV nucleic acid bases given • In young rats with chronic diarrhea, appearance and enzyme function of intestine greatly improved • Improved growth and maturation in young animals

  32. Infants given formula supplemented with nucleotides to mimic content of breast milk showed more benevolent intestinal flora an less diarrhea (50 times more nucleic acids in breast milk vs. formula which is significant in developing countries) • Supplemented infants had better lipid profiles with higher HDL cholesterol • Significant improvement in human cellular immune function • Significant improvement in memory in animals and humans • Accelerated wound healing

  33. ATP delivery specifically associated with numerous benefits • Improved pulmonary function, even in cystic fibrosis • Enhanced cardiac function – strengthening the heart • Relief of nerve pain and improved nerve conduction • Direct antitumor effects (RNA nucleotide) specifically incubation with ATP breast and prostate cancer

  34. Synergistic antitumor effects in conjunction with chemotherapy – in vitro studies suggest up to 90% dose reduction possible for certain cell types • IV ATP has halted progression of tumor cachexia (advanced cancer with rapid weight loss) 50 mcg/kg/minute x 24 hours x 3 weeks • Protection of tissues from radiation injury • Increased natural killer cell function • Survival of patients in ICU for shock (multi-organ failure) increased from 70% to 100%

  35. Current research Enhanced Nucleotide Supplementation

  36. Reducing Homocysteine reduces the risk of death from the top 5 killer diseases: Heart Attack by 80% Strokes by 82% Cancer by 33% Diabetes by ??% Alzheimer's by 50%

  37. Homocysteine Levels (units = micromoles/litre) Below 6.3 = Very Low Risk 6.4 - 9.0 = Low Risk 9.1 - 15.0 = High Risk + 15.0 = Very High Risk Every 5 point decrease in homocysteine level = 50% reduced risk of cardiovascular death 26% reduced risk of cancer death

  38. Methylation Formula Study Dose Response CurveHomocysteine Level- Treatment Group (n=22) Active Supplementation Group Months 0-3 11 10 9.2 9 8 7.1 7 6.8 P=.00001 6.1 6 P=.00001 P=.00001 0 1 2 3

  39. Methylation Formula Study Dose Response CurveHomocysteine Level- Placebo Group (n=11) 9 7.9 7.9 8 7.8 P= NS P= NS 7.3 7 P= NS 6 0 1 2 3

  40. Methylation Formula Study Dose Response CurveHomocysteine Level- Treatment Group for subjects with Baseline Homocysteine Level > 10 (n=7) Active Supplementation Group Months 0-3 14 13.2 12 10 9.3 8.3 P=.009 8 7.3 P=.001 P=.00001 0 1 2 3

  41. Population study completed in Western Norway with over 18,000 subjects – Hordaland Study Directly established a relation between homocysteine levels and chronological aging Homocysteine level of >13 was associated with someone 65 years old Homocysteine level of <7 was associated with someone 25 years old

  42. Bryan Maphalala - AIDS Victim Normal AIDS Brian

  43. Bryan Maphalala - AIDS Victim Before taking CELLFOOD and CELLFOOD DNA-RNA CD4 Count: 10 units; Viral Load: 201,000 After taking CELLFOOD & CELLFOOD DNA-RNA for 6 months Mrs. Winnie Mandela congratulated him for his work with HIV and AIDS people

  44. Does it really work?

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