Biohacking _Internal Processor



6 weeks ago, I began a daily regimen of LifeVantage Protandim, Tri-Synergizer. 12/02/202 marks my 60-day daily use of Protandim, Tri-synergizer.  I can say with confidence, Protandim has improved my overall sense of well being. I am sleeping more soundly, my mind is clearer, short term and long term memory have improved.


What is Protandim Tri-Synergizer?

Protandim® Tri-Synergizer™*
Protandim Nrf2, NAD, and NRF1 Synergizers effectively reduce oxidative stress, support mitochondria function, increase sirtuin activity, and target cell signaling pathways to fight the effects of aging.

The Protandim Family

LifeVantage is a company using science to approach health differently – we are focused on understanding the major scientific theories of aging and addressing the root causes to be able to take a proactive approach to increase healthspan.

We specialize in Nutrigenomics – using Nutrients to affect gene expression. Put simply, we use nutrients to tell our bodies how to help themselves.

It all started almost half a century ago, when science proved that our bodies have built in abilities to keep themselves healthy. Two decades ago, a discovery proved that we could tap into those abilities by communicating with our genes through nutrients.

That discovery is the reason LifeVantage exists. The discovery that five plant extracts, when used together, could tell your body to produce antioxidants*, opened a whole new world of possibilities. Since then we have been relentlessly working to communicate with additional genes associated with the major scientific theories of aging, and each subsequent discovery becomes a member of our flagship Protandim line of synergizers.




pierre-bamin-Red wrapping paper with bows and red raspberries and blueberries-unsplash

Holiday Gifts


A single blueberry image closeup by Michael Dziedzic from Unsplash

Our products are not intended to diagnose, treat, cure, or prevent disease or mitigate the symptoms of a disease. They are not drugs but dietary supplements. Supplements are intended only to supplement the human diet.

Pub published Peer-reviewed research strongly recommends these antioxidant producing powerhouses to combat oxidative stress sold exclusively by LifeVantage.  Click on the button below to learn more.

Joe Milton McCord (born March 3, 1945) is an American biochemist. While serving as a graduate student, he and his supervisor Irwin Fridovich were the first to describe the enzymatic activity of superoxide dismutase.[1][2] McCord joined the board of directors of the LifeVantage Corporation (makers of the dietary supplement Protandim) in 2006, serving as the company’s chief science officer from 2011 to 2012, and retired from the company in June 2013.[3]

Academic Background[edit]

McCord received a B.S. degree in chemistry from Rhodes College (graduated 1966) and a Ph.D. in biochemistry from Duke University (graduated 1970), where he also conducted postdoctoral research.[citation needed]

McCord is a past recipient of the Discovery Award from the Society for Free Radical Biology and Medicine (shared with Irwin Fridovich),[4] the Elliott Cresson Medal, and a Lifetime Achievement Award from the Oxygen Society.[citation needed]


McCord served on the board of directors (Director of Science) of the LifeVantage Corporation beginning in 2006[5] and was listed by the SEC as an insider shareholder.[6] LifeVantage is a Utah-based multilevel marketing company that distributes an antioxidant dietary supplement known as Protandim. McCord co-authored 7 studies on the product[7][8][9][10][11][12][13] and participated in distributor training.[6] McCord served as Chief Scientific Officer for LifeVantage from June 2011 until September 2012, and then became a member of the company’s science advisory board. LifeVantage announced McCord’s retirement in June 2013.[3][14] Under the terms of the separation agreement, McCord was to receive a payment of $1.7 million from the company.[14]


  1. ^ McCord JM, Fridovich I (November 1969). “Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein)”. J. Biol. Chem. 244 (22): 6049–55. PMID 5389100.
  2. ^ Keele BB, McCord JM, Fridovich I (November 1970). “Superoxide dismutase from escherichia coli B. A new manganese-containing enzyme”. J. Biol. Chem. 245 (22): 6176–81. PMID 4921969.
  3. ^ Jump up to:a b[full citation needed]
  4. ^ “SFRBM – Society for Free Radical Biology and Medicine”.
  5. ^[full citation needed]
  6. ^ Jump up to:a b[full citation needed]
  7. ^ Nelson SK, Bose SK, Grunwald GK, Myhill P, McCord JM (January 2006). “The induction of human superoxide dismutase and catalase in vivo: a fundamentally new approach to antioxidant therapy”. Free Radic. Biol. Med. 40 (2): 341–7. doi:10.1016/j.freeradbiomed.2005.08.043. PMID 16413416.
  8. ^ Velmurugan K, Alam J, McCord JM, Pugazhenthi S (February 2009). “Synergistic induction of heme oxygenase-1 by the components of the antioxidant supplement Protandim”. Free Radic. Biol. Med. 46 (3): 430–40. doi:10.1016/j.freeradbiomed.2008.10.050. PMID 19056485.
  9. ^ Liu J, Gu X, Robbins D, et al. (2009). “Protandim, a fundamentally new antioxidant approach in chemoprevention using mouse two-stage skin carcinogenesis as a model”. PLOS ONE. 4 (4): e5284. Bibcode:2009PLoSO…4.5284L. doi:10.1371/journal.pone.0005284. PMC 2668769. PMID 19384424.
  10. ^ Robbins D, Gu X, Shi R, et al. (2010). “The chemopreventive effects of Protandim: modulation of p53 mitochondrial translocation and apoptosis during skin carcinogenesis”. PLOS ONE. 5 (7): e11902. Bibcode:2010PLoSO…511902R. doi:10.1371/journal.pone.0011902. PMC 2912769. PMID 20689586.
  11. ^ Bogaard HJ, Natarajan R, Henderson SC, et al. (November 2009). “Chronic pulmonary artery pressure elevation is insufficient to explain right heart failure”. Circulation. 120 (20): 1951–60. doi:10.1161/CIRCULATIONAHA.109.883843. PMID 19884466.
  12. ^ Qureshi MM, McClure WC, Arevalo NL, et al. (June 2010). “The Dietary Supplement Protandim Decreases Plasma Osteopontin and Improves Markers of Oxidative Stress in Muscular Dystrophy Mdx Mice”. J Diet Suppl. 7 (2): 159–178. doi:10.3109/19390211.2010.482041. PMC 2926985. PMID 20740052.
  13. ^ Joddar B, Reen RK, Firstenberg MS, et al. (March 2011). “Protandim attenuates intimal hyperplasia in human saphenous veins cultured ex vivo via a catalase-dependent pathway”. Free Radic. Biol. Med. 50 (6): 700–9. doi:10.1016/j.freeradbiomed.2010.12.008. PMID 21167278.
  14. ^ Jump up to:a b “Form 8-K for LifeVantage Corp”. June 25, 2013. Retrieved 11/10/2013. Check date values in: |accessdate=(help)

External links