# Protective Effects of Microsorum scolopendria (Burm.f.) Copel. Leaf and Rhizome Extracts on Oxidative Stress and Inflammation Induced by Staphylococcus aureus and Staphylococcus epidermidis

**Authors:** Cristóbal Balada, Valentina Díaz, Mónica Castro, Macarena Echeverría-Bugueño, María José Marchant, Leda Guzmán

PMC · DOI: 10.3390/antiox14101194 · Antioxidants · 2025-09-30

## TL;DR

This study shows that extracts from the fern Microsorum scolopendria can protect skin cells from oxidative stress and inflammation caused by two types of bacteria.

## Contribution

The study demonstrates the protective effects of leaf and rhizome extracts of Microsorum scolopendria against bacterial-induced oxidative stress and inflammation in human skin cells.

## Key findings

- Pretreatment with extracts reduced reactive oxygen species (ROS) levels by up to 45% in infected cells.
- Extracts selectively inhibited COX-2, with rhizome extract showing 62% inhibition at 100 µg/mL.
- Rhizome extract showed modest cytotoxicity at intermediate concentrations but provided significant protection against membrane damage.

## Abstract

Microsorum scolopendria (Burm.f.) Copel. is a traditional medicinal fern with reported antioxidant and anti-inflammatory properties. In this study, we investigated the protective effects of leaf (HH) and rhizome (RH) extracts of MS on oxidative stress and inflammation in human dermal fibroblast (HDFa) cells infected with Staphylococcus aureus and Staphylococcus epidermidis. Cytotoxicity assays revealed that both extracts were safe up to 100 µg/mL, although RH exhibited a slight reduction in viability (≈20%) at 63 µg/mL. In infection assays, pretreatment with HH and RH extracts (63–100 µg/mL) for 3 h significantly reduced ROS levels by up to 45% compared with infected controls, while LDH release decreased by ~30%, indicating protection against membrane damage. Regarding anti-inflammatory activity, both extracts showed selective inhibition of COX-2 over COX-1, with RH inhibiting COX-2 by 62% and HH by 55% at 100 µg/mL, whereas COX-1 inhibition remained below 20%. These results highlight differential biological performance between leaf and rhizome extracts, with RH showing slightly higher anti-inflammatory activity but also a modest cytotoxic effect at intermediate concentrations. Overall, MS extracts demonstrated protective effects against oxidative and inflammatory damage induced by bacterial infection, supporting their potential as safe natural therapeutic agents for managing infection-associated skin stress and inflammation.

## Linked entities

- **Proteins:** COX1 (cytochrome c oxidase subunit I), COX2 (cytochrome c oxidase subunit II), Ldh (Lactate dehydrogenase)
- **Species:** Staphylococcus aureus (taxon 1280), Staphylococcus epidermidis (taxon 1282), Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** bacterial infection (MESH:D001424), Cytotoxicity (MESH:D064420), Inflammation (MESH:D007249), infection (MESH:D007239)
- **Chemicals:** ROS (-)
- **Species:** Microsorum scolopendria (species) [taxon 344756], Staphylococcus aureus (species) [taxon 1280], Staphylococcus epidermidis (species) [taxon 1282], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HDFa — Homo sapiens (Human), Finite cell line (CVCL_UF42)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12561396/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12561396/full.md

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Source: https://tomesphere.com/paper/PMC12561396