Methyl Nicotinate Is a Novel Geroprotective Compound That Promotes Mitochondria Dependent Lifespan Extension

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Abstract

Aging involves cellular decline and reduced stress resilience. We investigated geroprotective interventions using the yeast chronological aging model and identified methyl nicotinate (MN) as a potent lifespan-extending compound. MN enhanced cellular lifespan and stress resistance through mitochondria-dependent mechanisms, including AMPK/SNF1 signaling and HAP4 -mediated mitochondrial biogenesis. These benefits extended to human cells, improving their survival and mitochondrial function under aging conditions. Importantly, the effects of MN are linked to the NAD⁺ biosynthetic pathway, with its conversion to nicotinic acid (NA) and subsequent entry into the NAD⁺ salvage pathway being essential. We also identified the esterase IAH1 as a key enzyme for converting MN to NA in yeast. Our findings reveal MN as a conserved longevity compound, offering a new avenue for NAD + modulating anti-aging strategies.

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