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Micro- and Nanoplastics and Functional Nutrients in Human Health: Epigenetic Mechanisms and Cellular Resilience Signaling in Brain Insulin Resistance and the Risk of Alzheimer’s Disease

International Journal of Molecular Sciences 2025 1 citation ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Claudio Lombardo, Nicolò Musso, Paolo Giuseppe Bonacci, Gabriella Lupo, Carmelina Daniela Anfuso, Eleonora Di Fatta, Raffaele Ferri, Miroslava Majzúnová, Maria Scuto, Angela Trovato Salinaro, Angela Trovato Salinaro

Summary

This review explores how functional nutrients like polyphenols and flavonoids may help counteract damage caused by micro- and nanoplastic exposure, particularly regarding brain health. The study suggests these nutrients can activate protective cellular pathways at low doses to help maintain blood-brain barrier integrity, though chronic pollutant exposure may disrupt antioxidant signaling and contribute to brain insulin resistance.

Study Type In vitro

The therapeutic potential of functional nutrients has garnered considerable attention for enhancing resilience signaling and counteracting the damage to human health caused by microplastic pollutants. The intricate interactions between microplastics (MPs) and nanoplastics (NPs) and functional nutrients, including polyphenols, flavonoids, phenylpropanoids, phenolic acids, diterpenoids, and triterpenoids, have been shown to improve blood-brain barrier (BBB) homeostasis and brain function by inhibiting oxidative stress, ferroptosis, and inflammation linked to the pathogenesis of metabolic and brain disorders. Interestingly, nutrients exhibit biphasic dose-response effects by activating the nuclear factor erythroid 2-related factor 2 (Nrf2) pathway and stress-resilience proteins at minimum doses, thereby preventing or blocking MP and NP-induced damage. Notably, chronic exposure to environmental pollutants causes aberrant regulation of NFE2L2 gene and related antioxidant signaling, which can exacerbate selective susceptibility to brain insulin resistance under inflammatory conditions. This, in turn, impairs glucose metabolism and facilitates β-amyloid (Aβ) plaque synthesis leading to the onset and progression of Alzheimer's disease (AD), also known as "Type 3 diabetes". This pathological process triggered by oxidative stress, inflammation, and ferroptosis creates a vicious cycle that ultimately contributes to neuronal damage and loss. The review aims to investigate the therapeutic potential of functional nutrients targeting the Nrf2 pathway and stress resilience proteins to regulate epigenetic alterations, and to explore the underlying molecular mechanisms using innovative in vitro platforms for the development of promising preventive strategies and personalized nutritional interventions to attenuate oxidative stress, ferroptosis, and inflammation, with the goal of ultimately improving clinical outcomes.

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