# Nephroprotective Effect of Methanolic Extract of Micromeria frivaldszkyana (Degen) Velen Against Acetaminophen Overdose in Rats

**Authors:** Elisaveta Apostolova, Vesela Kokova, Ivica Dimov, Mariya Choneva, Delyan Delev, Ilia Kostadinov, Ilia Bivolarski, Maria Koleva, Tsvetelina Mladenova, Krasimir Todorov, Anelia Bivolarska

PMC · DOI: 10.3390/ijms27031547 · International Journal of Molecular Sciences · 2026-02-04

## TL;DR

This study shows that a plant extract from Micromeria frivaldszkyana protects rat kidneys from damage caused by high doses of acetaminophen.

## Contribution

This is the first study to evaluate the nephroprotective effects of Micromeria frivaldszkyana extract in an acetaminophen-induced kidney injury model.

## Key findings

- The extract significantly reduced serum urea, creatinine, and uric acid levels in APAP-treated rats.
- The extract restored glutathione levels and catalase activity while reducing lipid peroxidation markers.
- All tested doses of the extract showed significant nephroprotective effects.

## Abstract

Acetaminophen (APAP) overdose can induce potentially fatal nephrotoxicity. Micromeria frivaldszkyana (M. frivaldszkyana), an endemic plant to Bulgaria, has demonstrated significant antioxidant activity. This study represents the first evaluation of the nephroprotective effects of a methanolic extract of M. frivaldszkyana in an APAP-induced rat model of kidney injury. The aim of the study was to investigate the protective potential of orally administered M. frivaldszkyana methanolic extract against APAP-induced nephrotoxicity. Male Wistar rats received a one-week treatment with saline, M. frivaldszkyana extract (250, 400, or 500 mg/kg), rosmarinic acid (100 mg/kg), or silymarin (125 mg/kg). On day 7, renal injury was induced by oral administration of APAP (2000 mg/kg). Forty-eight hours later, blood and kidney samples were collected for biochemical and histological analyses. The extract at 500 mg/kg significantly reduced the elevated levels of serum urea (1.83 ± 0.24 vs. 3.49 ± 0.75, p < 0.05), creatinine (59.51 ± 2.30 vs. 72.27 ± 3.92, p < 0.05), and uric acid (477.55 ± 52.48 vs. 898.33 ± 65.30, p < 0.001), while restoring renal glutathione (GSH) levels (4.43 ± 0.19 vs. 2.64 ± 0.10, p < 0.001) and catalase activity (3802.78 ± 142.05 vs. 2485.03 ± 143.23, p < 0.01), compared with APAP-treated rats. Malondialdehyde levels were significantly reduced by the extract (25.19 ± 0.95 vs. 69.66 ± 4.11, p < 0.001), with similar effects observed across all tested doses. In conclusion, M. frivaldszkyana methanolic extract confers significant protection against APAP-induced nephrotoxicity, likely through antioxidant-mediated mechanisms, enhanced GSH restoration, and attenuation of lipid peroxidation, highlighting its potential as a nephroprotective agent.

## Linked entities

- **Proteins:** Cat (Catalase)
- **Chemicals:** acetaminophen (PubChem CID 1983), urea (PubChem CID 1176), creatinine (PubChem CID 588), uric acid (PubChem CID 1175), glutathione (GSH) (PubChem CID 124886)

## Full-text entities

- **Genes:** Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}
- **Diseases:** kidney injury (MESH:D007674), Overdose (MESH:D062787)
- **Chemicals:** silymarin (MESH:D012838), lipid (MESH:D008055), GSH (MESH:D005978), uric acid (MESH:D014527), creatinine (MESH:D003404), Degen (-), urea (MESH:D014508), rosmarinic acid (MESH:C041376), Malondialdehyde (MESH:D008315), APAP (MESH:D000082)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12898259/full.md

## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC12898259/full.md

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Source: https://tomesphere.com/paper/PMC12898259