ArticlePhotochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology2026
Schisandrin A alleviates UVB-induced photoaging via AMPK/Nrf2-mediated antioxidant and autophagy pathways.
Article in Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Skin photoaging, primarily induced by chronic UVB exposure, lacks effective therapeutic options. Schisandrin A (Sch A), a bioactive compound from Schisandra chinensis, has been traditionally used in East Asian medicine for its anti-inflammatory and antioxidant properties. However, the precise mechanisms by which Sch A exerts photoprotective effects against UVB-induced damage remain unclear, warranting further mechanistic exploration. This study aimed to explore the protective effects of Sch A against UVB-induced damage in HaCaT keratinocytes and ICR mice. Sch A improved cell viability, reduced senescence and apoptosis, and enhanced antioxidant defenses by increasing SOD activity and GSH levels while reducing MDA accumulation in mice. Histological analysis showed that Sch A decreased epidermal thickness and preserved dermal collagen. Molecular assays revealed that Sch A activated AMPK and Nrf2 signaling, promoted autophagy, reduced oxidative stress, and inhibited MMP expression. These findings suggest that Sch A alleviates photoaging by modulating oxidative stress, apoptosis, and autophagy via the AMPK/Nrf2 pathways, offering a promising strategy for skin protection.
Indexed as
Identifiers
41801672What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.