Subcellular photoprotection through precision nutraceuticals: Divergent actions of rutin and punicalagin on redox and mitochondrial homeostasis in human dermal fibroblasts

氧化应激 芦丁 氧化磷酸化 化学 生物化学 抗氧化剂 线粒体 线粒体分裂 细胞保护 光老化 细胞生物学 谷胱甘肽 蛋白质稳态 活性氧 脂质过氧化 光防护 姜黄素 KEAP1型 超氧化物歧化酶 脂质氧化 保健品 线粒体ROS 药理学
作者
Alessia Riente,Flavio Di Giacinto,Michele Maria De Giulio,Benedetta Niccolini,Elisabetta Tabolacci,Maria Elisabetta Clementi,Marco De Spirito,Giuseppe Maulucci
出处
期刊:Journal of Photochemistry and Photobiology B-biology [Elsevier BV]
卷期号:278: 113429-113429 被引量:1
标识
DOI:10.1016/j.jphotobiol.2026.113429
摘要

Excessive ultraviolet A (UVA) exposure is a major environmental factor contributing to skin photoaging and oxidative damage. Identifying natural compounds that can counteract these effects is increasingly relevant for preventive and personalized healthcare. Precision nutrition uses diet-derived bioactives to modulate molecular pathways in defined cellular contexts. Polyphenols are promising for sustaining redox and metabolic balance under stress. This study examined the photoprotective actions of rutin (buckwheat, citrus peel) and punicalagin (pomegranate) in human dermal fibroblasts exposed to UVA radiation. Phasor-based fluorescence lifetime imaging microscopy (FLIM) quantified lipid peroxidation–related oxidative stress ( F ox ) and oxidative phosphorylation activity ( F oxphos ). Mitochondrial morphology was assessed via fission (Fis1) and fusion (MFN2) markers. Though UVA exposure tended to increase oxidative stress, the observed variation is not significant. Rutin provided superior antioxidant protection under UVA stress, substantially reducing F ox to 0.129 ± 0.02 with a near-significant trend, while punicalagin demonstrated stronger baseline antioxidant activity. Both compounds enhanced oxidative phosphorylation under stress: punicalagin increased F oxphos to 0.823 ± 0.02 ( p = 0.004 vs UVA) and rutin to 0.789 ± 0.02 ( p = 0.023 vs UVA). UVA disrupted mitochondrial networks, elevating fission and reducing fusion. Rutin reversed these effects, restoring fusion and reducing fission, whereas punicalagin provided partial recovery. In summary, rutin offered broader cytoprotection by mitigating oxidative stress and preserving mitochondrial integrity, while punicalagin mainly supported metabolic activity. These distinct responses highlight polyphenol-based nutraceuticals as precision tools for targeted skin photoprotection, suggesting their potential use in dietary or topical formulations to counteract everyday UVA exposure and photoaging.

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