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Each bioactive addresses a distinct yet intersecting node of dysfunction, i.e., vitamin D attenuates NF-B-mediated inflammation and enhances insulin signaling through VDR-dependent transcriptional control, MI restores inositolphosphoglycan second-messenger activity, normalizing PI3K/Akt signaling and reducing hyperinsulinemia, and melatonin stabilizes mitochondrial function, activates Nrf2-dependent antioxidant defenses, and re-aligns circadian regulation of the HPO axis
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This hypothesis is supported by the study of Calvano et al
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