# From Reshaped Metabolome to Repaired Skin: Fermented Gastrodia elata Alleviates UVB-Induced Damage Through Controlled Immune Activation

**Authors:** Xing Huang, Xiaoqi Yang, Chunrui Xu, Jiajia Liu, Yuan Luo, Zixian Xu, Shixiao Pu, Zongyang Li, Yunlong Zhang, Min Bai, Lianbing Lin

PMC · DOI: 10.3390/antiox15010045 · Antioxidants · 2025-12-29

## TL;DR

Fermented Gastrodia elata protects skin from UVB damage by boosting antioxidants and balancing inflammation in mice.

## Contribution

GL shows superior anti-inflammatory and antioxidant effects compared to vitamin E through unique metabolic and immune pathways.

## Key findings

- GL treatment improved skin morphology and antioxidant activity in UVB-exposed mice.
- GL activated NOD-like receptor pathways and induced Tnfaip3 for immune regulation.
- Fermentation enriched collagen-related metabolites and anti-inflammatory compounds.

## Abstract

UVB radiation induces cutaneous damage through oxidative stress and immune dysregulation. This study investigated the therapeutic potential of Gastrodia elata fermented by Lactobacillus salivarius AACE1 (GL) in a mouse model of UVB-induced skin injury. Results demonstrated that GL treatment significantly improved skin morphology, enhanced antioxidant activities (SOD and GSH), reduced oxidative damage (MDA), and balanced inflammatory mediators by upregulating TGF-β and IL-10 while downregulating TNF-α, IL-6, and IL-1β. Transcriptomic analysis revealed that GL specifically activated NOD-like receptor signaling pathway components (Nlrp3, Casp4, and Gbp2/5) while inducing Tnfaip3 to establish negative feedback control. Metabolomic profiling confirmed that fermentation transformed the metabolite landscape, enriching collagen-related dipeptides, antimicrobial/anti-inflammatory metabolites, and antioxidant cofactors. Importantly, comparative analysis showed that GL is more effective than vitamin E in coordinating multiple signaling pathways and maintaining inflammatory homeostasis. These findings establish GL as an effective natural product that alleviates UVB-induced skin damage through synchronized metabolic remodeling and controlled immune activation.

## Linked entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], IL10 (interleukin 10) [NCBI Gene 3586], TNF (tumor necrosis factor) [NCBI Gene 7124], IL6 (interleukin 6) [NCBI Gene 3569], IL1B (interleukin 1 beta) [NCBI Gene 3553], NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548], CASP4 (caspase 4) [NCBI Gene 837], GBP2 (guanylate binding protein 2) [NCBI Gene 2634], GBP5 (guanylate binding protein 5) [NCBI Gene 115362], TNFAIP3 (TNF alpha induced protein 3) [NCBI Gene 7128]
- **Chemicals:** GSH (PubChem CID 124886), MDA (PubChem CID 1614)
- **Species:** Gastrodia elata (taxon 91201), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), skin damage (MESH:D012871), immune dysregulation (OMIM:614878), skin injury (MESH:D000069836)
- **Chemicals:** vitamin E (MESH:D014810), MDA (MESH:D015104), AACE1 (-), dipeptides (MESH:D004151)
- **Species:** Gastrodia elata (species) [taxon 91201], Mus musculus (house mouse, species) [taxon 10090], Ligilactobacillus salivarius (species) [taxon 1624]

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12837383/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12837383/full.md

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Source: https://tomesphere.com/paper/PMC12837383