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Frontiers in Natural Products· 2026Q2

Protective effects of an aqueous extract from Pinctada fucata martensii mucus on ultraviolet A-induced skin photoaging: in vitro and in vivo evidence

Anqi Cao, Xiaohui Wang, Siwei Quan, Yingfa Qin et al.

Short summary

An aqueous extract (AKN) from Akoya pearl oyster mucus significantly protects against UVA-induced skin photoaging by suppressing senescence markers, inflammation, and oxidative stress, and restoring collagen in mice.

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Key points

  • Aqueous extract (AKN) from Pinctada fucata martensii mucus contains taurine (8.0%) and betaine (4.1%).
  • AKN suppressed p16, p21, p53, Tnf, Il6, Il1b, and ROS in UVA-exposed cells.
  • Topical AKN (4 mg/mL) restored Col1a1 transcription and improved skin histology in a mouse photoaging model.
  • AKN protected against epidermal hyperplasia and collagen depletion, comparable to ergothioneine.

AI-generated from the title and abstract; the full text is not read.

Abstract

Ultraviolet A (UVA) radiation is a primary extrinsic driver of skin photoaging, yet effective marine-derived photoprotective countermeasures remain underexplored. The Akoya pearl oyster ( Pinctada fucata martensii, Pinctada martensii ) mucus represents a largely underexplored source of water-soluble marine natural products. In the present study, a low-molecular-weight aqueous fraction (designated AKN) was prepared via direct aqueous extraction and 3 kDa ultrafiltration without enzymatic hydrolysis, preserving the native constituent profile. AKN was systematically profiled using orthogonal untargeted LC–MS and targeted compositional analyses, with taurine and betaine accounting for 8.0% and 4.1% of the dry weight, respectively. Its biological effects were evaluated in UVA-exposed L929 murine fibroblasts, LPS-stimulated BV2 murine microglial cells, and a UVA-induced BALB/c mouse skin photoaging model, using ergothioneine (EGT) as a positive control. In cellular assays, AKN markedly suppressed the expression of key senescence regulators ( p16, p21, p53 ), attenuated pro-inflammatory mediators ( Tnf, Il6, Il1b ), and reduced intracellular reactive oxygen species. In mouse skin, topical AKN restored Col1a1 transcription and improved histological architecture by suppressing epidermal hyperplasia and collagen depletion, with 4 mg/mL AKN providing pronounced protection alongside 4 mg/mL ergothioneine. Overall, these findings establish P. martensii mucus as a promising source of natural, hydrolysis-free photoprotective agents and support further bioassay-guided identification of its primary active constituents.

The authors' abstract, as published at the source. Frontiers in Natural Products, 2026 · DOI ↗

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