Vitamin B3 (Niacin)

Vitamin B3 – Joints Need Vitamin B3

Vitamin B3 describes a group of molecules with very similar chemical structures. There are two principal forms: Niacin and Niacinamide. Once digested, both molecules travel down similar metabolic pathways and are converted to functionally equivalent, biologically active compounds that are vital for health. Vitamin B3 is a crucial building block for two vital coenzymes in the human body: Nicotinamide Adenine Dinucleotide (NAD) and Nicotinamide Adenine Dinucleotide Phosphate (NADP). In general, NAD and NADP play a paramount role in energy transfer. NAD contributes to energy production from the breakdown of nutrients, such as carbohydrates, fats, and proteins. Conversely, NADP predominantly participates in reactions that build new molecules, such as those in cartilage, bone, muscle, and tendon.

Vitamin B3 is water-soluble. Since it is water-soluble, the body cannot store it like other nutrients. Without storage, the body only gets the health benefits of B3 when it is consumed.

Musculoskeletal Health Benefits of Vitamin B3

1. Vitamin B3 Supports Joint Health

Vitamin B3 end products NAD and NADP are crucial molecules that support cartilage DNA health, maintenance, and growth. When cartilage cell DNA is damaged, enzymes that depend on NAD and NADP are activated to initiate and manage the repair process. In unhealthy joints, cartilage cells have significantly more DNA damage compared to healthy joints. Without adequate NAD and NADP, DNA repair is hindered. Also, oxygen is relatively scarce in cartilage due to its limited blood supply. Vitamin B3 end products can help enhance non-oxygen-dependent energy pathways, ensuring cartilage cells have enough fuel for health, repair, and growth.

2. Vitamin B3 Demonstrates Antioxidant Activity

Vitamin B3 derivatives help neutralize dangerous free radicals that attack protein, fats, and DNA. Free radical damage is linked to unhealthy joints, bones, muscles, and tendons. Additionally, Vitamin B3 promotes a healthy immune response to injury. Chronic unhealthy immune responses to damaged tissue can accelerate and magnify cell injury and dysfunction.

Selected Evidence

To test the theory that greater consumption of niacinamide diminishes symptoms of osteoarthritis, researchers from the National Institutes of Health performed a randomized, double-blinded, placebo-controlled study. Seventy-two patients, average age 65, were randomly assigned to two groups. The treatment group received niacinamide supplementation (3,000 mg/day for three months) while the placebo group received a dummy pill for the same duration. After 12 weeks, the treatment group showed close to a 30% improvement in their global arthritis impact scores, which measures overall function and pain (Jonas et al., Inflamm Res 45:330-334).

Japanese scientists analyzed dietary habits of over 500 Japanese women and found an association between low dietary vitamin B3 intake and knee osteoarthritis. The average intake was 13.8 mg/day, just below the recommended dietary allowance (Muraki et al., Mod Rheumatol. 2014 Mar;24(2):236-42).

Precautions

Vitamin B3 from natural foods is generally well tolerated. RDA amounts are typically obtained from a balanced diet. An upper limit of 35 mg/day is set mainly to prevent skin flushing. Other potential side effects of high-dose supplementation include gastrointestinal disturbances and liver toxicity. Consult a healthcare professional before supplementing, particularly if you have specific health conditions.

References

  1. (2017). Niacin. Micronutrient Information Center. Retrieved from http://lpi.oregonstate.edu/mic/vitamins/niacin
  2. (2017). Vitamin B3 – niacin. The World’s Healthiest Foods. Retrieved from http://www.whfoods.com/genpage.php?tname=nutrient&dbid=83
  3. Jonas, W. B., Rapoza, C. P., & Blair, W. F. (1996). The effect of niacinamide on osteoarthritis: A pilot study. Inflammation Research, 45(7), 330-334.
  4. Muraki, S., Akune, T., En-yo, Y., Yoshida, M., Tanaka, S., Kawaguchi, H., & Yoshimura, N. (2014). Association of dietary intake with joint space narrowing and osteophytosis at the knee in Japanese men and women: The ROAD study. Modern Rheumatology, 24(2), 236-242. https://doi.org/10.3109/14397595.2013.854055
  5. Otten, J. J., Hellwig, J. P., & Meyers, L. D. (Eds.). (2006). Dietary reference intakes: The essential guide to nutrient requirements. Washington, D.C.: National Academy of Sciences.
  6. Thorne Research, Inc. (2002). Niacinamide. Alternative Medicine Review, 7(6), 525-529.
  7. Kröger, H., Hauschild, A., Ohde, M., Bache, K., Voigt, W. P., & Ehrlich, W. (1999). Enhancing the inhibitory effect of nicotinamide upon collagen II induced arthritis in mice using N-acetylcysteine. Inflammation, 23(2), 111-115.
  8. Kröger, H., Miesel, R., Dietrich, A., Ohde, M., Rajnavölgyi, E., & Ockenfels, H. (1996). Synergistic effects of thalidomide and poly (ADP-ribose) polymerase inhibition on type II collagen-induced arthritis in mice. Inflammation, 20(2), 203-215.
  9. Présumey, J., Courties, G., Louis-Plence, P., Escriou, V., Scherman, D., Pers, Y. M., Yssel, H., Pène, J., Kyburz, D., Gay, S., Jorgensen, C., & Apparailly, F. (2013). Nicotinamide phosphoribosyltransferase/visfatin expression by inflammatory monocytes mediates arthritis pathogenesis. Annals of the Rheumatic Diseases, 72(10), 1717-1724. https://doi.org/10.1136/annrheumdis-2012-202403
  10. Hoffer, A. (1959). Treatment of arthritis by nicotinic acid and nicotinamide. Canadian Medical Association Journal, 81, 235-238.
  11. McCarty, M. F., & Russell, A. L. (n.d.). Niacinamide therapy for osteoarthritis—does it inhibit nitric oxide synthase induction by interleukin 1 in chondrocytes?
  12. Olofsson, P., Nerstedt, A., Hultqvist, M., Nilsson, E. C., Andersson, S., Bergelin, A., & Holmdahl, R. (2007). Arthritis suppression by NADPH activation operates through an interferon-beta pathway. BMC Biology, 5, 19. https://doi.org/10.1186/1741-7007-5-19

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