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Furthermore, both human primary CD34+ cells treated with IS and a mouse model with 5/6 Nx exhibited a blockage at the BFU-E stage of erythropoiesis

Over-dosed: This is the more concerning scenario

What they found (summary): NAD+ is the integrator of metabolic and stress signals The decline in NAD+ with age is a causal factor , not merely a correlation PARP and CD38 are the main consumers of NAD+ in aging cells Selective CD38 inhibitors are a new therapeutic option NAD+ has potential in neurodegeneration (Alzheimers, Parkinsons, ALS) Why it matters: Verdins review in Science gave the NAD+ field academic prestige

Abnormal Ca influx impairs energy production and activates caspase proteins, initiating the intrinsic apoptotic pathway and accelerating cardiomyocyte loss [134, 135]