# Anti-Inflammatory, Antinociceptive, and LC-MS Metabolic Profile from Pseudotrimezia juncifolia (Klatt) Lovo & A. Gil

**Authors:** Alan Silva Minho, Pamela Gomes de Almeida, Natália Naomi Kato, Ana Laura Macedo Brand, Roberto Fontes Vieira, Rafael Garrett, Norberto Peporine Lopes, Claudia Moraes Rezende, Patricia Dias Fernandes

PMC · DOI: 10.3390/ph17081101 · Pharmaceuticals · 2024-08-22

## TL;DR

This study explores the anti-inflammatory and pain-relieving properties of Pseudotrimezia juncifolia and identifies its active compounds using metabolic profiling.

## Contribution

The paper provides empirical evidence of the plant's biological activities and links them to specific phenolic compounds through LC-MS/MS analysis.

## Key findings

- Decoctions of Pseudotrimezia juncifolia reduced nociception in mice via antinociceptive effects.
- The plant extract demonstrated anti-inflammatory activity by reducing cytokine production and cell migration.
- Metabolomic analysis revealed a high concentration of phenolic compounds, including flavonoids and chlorogenic acids.

## Abstract

Pseudotrimezia juncifolia (Klatt) Lovo & A. Gil (Iridaceae) is a popularly known species with primarily ornamental economic interest. It has traditional uses as purgative, in conditions related to the menstrual cycle, for blood purification, as wound healing, and as anti-inflammatory. The anti-inflammatory and antinociceptive activities of the decoction from its aerial stems, corms, and stamens are described here with dereplication studies on LC-MS/MS supported by the GNPS platform, where phenolic compounds were annotated and correlated with its biological activity. The decoction was evaluated in chemical (formalin and capsaicin) and thermal (hot plate) induced nociception or carrageenan-induced inflammation in mice. Decoction (at 10, 30, or 100 mg/kg doses) significantly reduced formalin- or capsaicin-induced nociception. All doses also demonstrated an antinociceptive effect in the hot plate model increasing the time the animal spent in responding to thermal signal. Naloxone partially reversed the antinociceptive effect. An anti-inflammatory effect was observed since a reduction in cell migration, protein extravasation interleukin-1, and tumor necrosis factor production induced by carrageenan in the subcutaneous air pouch was quantified. Metabolomic analyses showed a predominance of phenolic substances, mainly flavonoids and chlorogenic acids. The literature showed that these two groups have significant anti-inflammatory and analgesic activity, and chemical data corroborate the pharmacological results observed.

## Linked entities

- **Chemicals:** formalin (PubChem CID 712), capsaicin (PubChem CID 1548943)
- **Species:** Pseudotrimezia juncifolia (taxon 1201204), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}
- **Diseases:** Inflammatory (MESH:D007249)
- **Chemicals:** Naloxone (MESH:D009270), carrageenan (MESH:D002351), chlorogenic acids (MESH:D002726), formalin (MESH:D005557), phenolic compounds (-), capsaicin (MESH:D002211), flavonoids (MESH:D005419)
- **Species:** Pseudotrimezia juncifolia (species) [taxon 1201204], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11359133/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC11359133/full.md

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Source: https://tomesphere.com/paper/PMC11359133