# Anti-Photoaging Effect of Pinctada martensii Hydrolysates on Ultraviolet B-Irradiated Nude Mice Skin

**Authors:** Mengfen Wei, Dongcheng Liu, Shiyuan Chang, Lijun You, Oliy Akhmedov

PMC · DOI: 10.3390/md24030097 · 2026-02-28

## TL;DR

This study shows that Pinctada martensii hydrolysates reduce UVB-induced skin damage in mice, suggesting potential for functional foods targeting photoaging.

## Contribution

The study demonstrates the anti-photoaging effects of Pinctada martensii hydrolysates in a UVB-induced mouse model, including gut-skin axis modulation.

## Key findings

- PME reduced epidermal thickness and restored dermal collagen content in UVB-exposed mice.
- PME suppressed UVB-induced upregulation of MMP-1, MMP-3, and MMP-9 by 61%, 65%, and 52%, respectively.
- PME treatment modulated gut microbiota and increased short-chain fatty acids, suggesting involvement of the gut-skin axis.

## Abstract

Pinctada martensii is a marine resource with potential for bioactive peptide development, but its anti-photoaging properties remain underexplored. In this study, Pinctada martensii meat hydrolysates (PME) were prepared by enzymatic hydrolysis, and their anti-photoaging effects were evaluated in an in vivo ultraviolet-B (UVB)-irradiated nude mouse model. The results showed that PME markedly ameliorated UVB-induced skin damage. UVB increased epidermal thickness from 21.60 μm in the Control to 47.50 μm in the Model, and PME reduced epidermal thickness to 22.46 μm. Dermal collagen content decreased from 64.58% in the Control to 26.22% in the Model and was restored to 52.75% by PME. UVB upregulated matrix metalloproteinases-1 (MMP-1), MMP-3 and MMP-9 by approximately 2.20-, 1.93- and 3.09-fold relative to the Control, and PME suppressed these matrix metalloproteinases (MMPs) by approximately 61%, 65% and 52%, respectively. Extracellular signal-regulated kinase (ERK) expression increased to 1.41-fold in the Model and was reduced to about 1.05-fold after PME treatment, suggesting inhibition of collagen degradation-related pathways. Untargeted serum metabolomics identified 205 differential metabolites between the Model and the Control, and PME shifted metabolite profiles toward those of the Control. Total short-chain fatty acids (SCFAs) decreased from 868.69 μmol/g in the Control to 301.34 μmol/g in the Model and increased to approximately 562 μmol/g after PME treatment, accompanied by modulation of the gut microbiota including recovery of Lachnospiraceae members, indicating involvement of the gut–skin axis. These findings support the potential of Pinctada martensii meat as a source for developing novel functional foods targeting skin photoaging.

## Linked entities

- **Proteins:** MMP1 (matrix metallopeptidase 1), MMP3 (matrix metallopeptidase 3), MMP9 (matrix metallopeptidase 9)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Eln (elastin) [NCBI Gene 13717] {aka E030024M20Rik}, Hcar2 (hydroxycarboxylic acid receptor 2) [NCBI Gene 80885] {aka Gpr109a, Gpr109b, HM74, Niacr1, PUMA-G, Pumag}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, Mapk1 (mitogen-activated protein kinase 1) [NCBI Gene 26413] {aka 9030612K14Rik, ERK, Erk2, MAPK2, PRKM2, Prkm1}, Phex (phosphate regulating endopeptidase homolog, X-linked) [NCBI Gene 18675] {aka Gy, HPDR, HPDR1, Hyp, PEX}, Ffar3 (free fatty acid receptor 3) [NCBI Gene 233080] {aka Gm478, Gpr41}, Vip (vasoactive intestinal polypeptide) [NCBI Gene 22353], Ffar2 (free fatty acid receptor 2) [NCBI Gene 233079] {aka GPCR43, Gpr43}, Fn1 (fibronectin 1) [NCBI Gene 14268] {aka E330027I09, Fn, Fn-1}, Mmp3 (matrix metallopeptidase 3) [NCBI Gene 17392] {aka EMS-2, MMP-3, SL-1, SLN-1, SLN1, STR-1}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Mmp13 (matrix metallopeptidase 13) [NCBI Gene 17386] {aka Clg, MMP-13, Mmp1}
- **Diseases:** weight loss (MESH:D015431), dislocation (MESH:D004204), melanoma (MESH:D008545), actinic elastosis (MESH:D005148), epidermal hyperplasia (MESH:D006965), skin damage (MESH:D012871), inflammation (MESH:D007249), pigmentation disorders (MESH:D010859), metabolic disturbances (MESH:D024821), actinic keratosis (MESH:D055623), death (MESH:D003643), dryness (MESH:D014987), injury to (MESH:D014947), toxicity (MESH:D064420), Dysbiosis (MESH:D064806)
- **Chemicals:** Ubiquinone (MESH:D014451), glutamic acid (MESH:D018698), Valine (MESH:D014633), (-)-Norephedrine (MESH:D010665), amino acid (MESH:D000596), PBS (MESH:D007854), balsam (MESH:D001453), leucine (MESH:D007930), asparagine (MESH:D001216), GSH (MESH:D005978), formalin (MESH:D005557), acetonitrile (MESH:C032159), CoA (MESH:D003065), isoleucine (MESH:D007532), 3-Hydroxyanthranilic Acid (MESH:D015095), L-methionine S-oxide (MESH:C013111), Paraffin (MESH:D010232), L-lysine (MESH:D008239), water (MESH:D014867), BCA (MESH:C047117), Glycerophospholipid (MESH:D020404), isopropanol (MESH:D019840), Glycine (MESH:D005998), androsterone glucuronide (MESH:C027927), EGCG (MESH:C045651), SCFA (MESH:D005232), proline (MESH:D011392), N2 (MESH:D009584), L-tyrosine (MESH:D014443), Butyrate (MESH:D002087), Acetate (MESH:D000085), Pantothenate (MESH:D009536), formic acid (MESH:C030544), Nicotinate (MESH:D009525), Steroid hormone (MESH:D013256), polyphenols (MESH:D059808), carbohydrates (MESH:D002241), hematoxylin (MESH:D006416), carbon (MESH:D002244), N-acetyl-L-phenylalanine (MESH:C044228), Aminoacyl-tRNA (MESH:D012346), ethanol (MESH:D000431), threonine (MESH:D013912), terpenoid (MESH:D013729), Hydroxyproline (MESH:D006909), hydrogen (MESH:D006859), Citrate (MESH:D019343), Pyrimidine (MESH:C030986), N-formyl-L-methionine (-), quinone (MESH:C004532), serine (MESH:D012694), Phenylalanine (MESH:D010649), propionate (MESH:D011422), EDTA (MESH:D004492), 2-Hydroxyphenylacetic Acid (MESH:C005756), N6-acetyl-L-lysine (MESH:C016949), xylene (MESH:D014992), Galactose (MESH:D005690), Propionic acid (MESH:C029658), Tryptophan (MESH:D014364)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Actinomycetota (actinobacteria, phylum) [taxon 201174], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Eubacterium (genus) [taxon 1730], Occidozyga martensii (Marten's oriental frog, species) [taxon 146711], Bacteroides (genus) [taxon 816], Enterorhabdus (genus) [taxon 580024], Gemella (genus) [taxon 1378], Pinctada imbricata (Akoya pearl oyster, species) [taxon 66713], [Eubacterium] nodatum (species) [taxon 35518], Lactobacillus (genus) [taxon 1578], Patescibacteria group (clade) [taxon 1783273], Staphylococcus (genus) [taxon 1279], Lachnoclostridium (genus) [taxon 1506553], Parvibacter (genus) [taxon 1427376], Prevotellaceae (family) [taxon 171552], Mus musculus (house mouse, species) [taxon 10090], Negativibacillus (genus) [taxon 1980693], Desulfovibrio (genus) [taxon 872], Roseburia (genus) [taxon 841], Homo sapiens (human, species) [taxon 9606], Erysipelatoclostridium [taxon 1505663], Crassostrea hongkongensis [taxon 298176]
- **Cell lines:** /c — Mus musculus (Mouse), Hepatocellular carcinoma of the mouse, Cancer cell line (CVCL_9103), HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038)

## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027452/full.md

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Source: https://tomesphere.com/paper/PMC13027452