Study to Evaluate the Effect of Nicotinamide Riboside on Immunity

Intermittent caloric restriction or fasting has numerous health effects including the reduction in numerous cardiovascular disease risk factors. The cellular programs activated by caloric restriction are similarly turned on in preclinical studies in response to a 24-hour fast. We have found that a beneficial effect of 24-hour fasting is that it blunts the activation of a component of the immune system, termed the Nod-like receptor family protein 3 (NLRP3) Inflammasome. This inflammasome, as a mediator of sterile inflammation, is associated with the development of diabetes and atherosclerosis. At the same time, we found that refeeding after the 24-hour fast significantly increased NLRP3 protein levels, IL-1Beta, and TNF signaling, and that fasting blunted the NLRP3 inflammasome response, in association with the activation of a fasting sensing protein called SIRT3. Interestingly, a recently discovered naturally occurring form of vitamin B3, called nicotinamide riboside (NR), has been found to activate SIRT3. We found that NR reproduces the NLRP3 inflammasome blunting effect of fasting when administered to primary human monocytes/macrophages in culture. Putting this together, it would be interesting to evaluate whether the administration of NR to human subjects would replicate the fasting blunting effect on the NLRP3 inflammasome. Interestingly, at the same time, it has recently been found, in a preclinical study, that the NLRP3 protein can orchestrate differentiation of naive T- cells into Th2 cells. We therefore propose to more broadly examine the effects of NR administration on myeloid and lymphoid cell biology in healthy volunteers.

• INCLUSION CRITERIA:

As this is a pilot study, the age-range and BMI range of subjects will be restricted to potentially reduce metabolic variables associated with a wide age- and BMI-range.

• Males and females between the ages of 18 and 39
• BMI between 18.5 and 29.9
• Agrees to comply with study procedures and maintain current level of physical activity and dietary intake throughout the study.
• Female subjects of child-bearing ability willing to commit to reliable contraception while participating in the study.

Exclusion criteria

• Subjects with an acute or chronic illness as per history, on laboratory analysis or requiring medications to manage disease.
• Subjects taking vitamins or supplements or any medications, except oral contraceptives, within 4 weeks of participation into this study.
• BMI <18.5 or >29.9.
• Female subjects who are pregnant or lactating.
• Subjects who have donated blood or participated in another clinical trial involving blood draws in the last 8 weeks.
• Subjects who use nicotine products including chewing tobacco, vaporizer, gum, cigarette or patch form within three months.
• Any other medical condition that, in the opinion of the Principal Investigator, might put the subject at risk of harm during the study or might adversely affect the interpretation of the study data.