# Anti‐Inflammatory and Lipid Metabolism Modulatory Effects of Lantana camara L. Extract, With Enhanced Fibroblast Migration

**Authors:** Ari S. de O. Lemos, Matheus T. Branca, Lara M. Campos, Natasha S. Mayrink, Lívia R. Gamarano, João Pedro R. C. Bastos, Ana Julia de Almeida, Elaine S. Coimbra, Rodrigo L. Fabri

PMC · DOI: 10.1002/cbdv.202501335 · 2025-12-15

## TL;DR

This study shows that Lantana camara extract reduces inflammation and boosts fibroblast migration, suggesting it could be a natural treatment for inflammation and wound healing.

## Contribution

The study reveals Lantana camara's anti-inflammatory and fibroblast-promoting effects, with specific impacts on lipid metabolism and macrophage activity.

## Key findings

- LCE significantly reduced NO, ROS, and LB formation in macrophages.
- LCE lowered levels of TNF-α, TGF-β, and PGE2, indicating anti-inflammatory activity.
- LCE enhanced fibroblast migration by 86.26% in a wound healing assay.

## Abstract

Inflammation is a complex process associated with various chronic diseases. Lantana camara L., widely used in traditional medicine, exhibits diverse bioactivities, though its effects on lipid metabolism, prostaglandin E2 (PGE2) production in macrophages, and fibroblast migration remain unclear. This study aimed to evaluate whether the ethanolic extract from L. camara leaves (LCE) influences these processes. Phytochemical analysis by an ultra‐fast liquid chromatography‐quadrupole time of flight mass spectrometry identified flavonoids and iridoid glycosides in the extract. Cytotoxicity assays using BALB/c mouse peritoneal macrophages and L929 fibroblasts showed no significant effect on cell viability. Anti‐inflammatory activity was assessed through nitric oxide (NO), reactive oxygen species (ROS), lipid bodies (LB), and levels of tumor necrosis factor (TNF)‐α, transforming growth factor (TGF)‐β, and PGE2. LCE significantly reduced NO (74.61 ± 5.08%), ROS (58.38 ± 1.77%), and LB formation (53.56 ± 3.33%), as well as TNF‐α (40.63 ± 1.33%), TGF‐β (88.96 ± 12.87%), and PGE2 (56.88 ± 27.10%) levels. Wound healing potential was evaluated via scratch assay, with LCE promoting fibroblast migration up to 86.26 ± 0.81% after 48 h. These findings indicate that LCE modulates macrophage inflammatory responses and promotes tissue repair, supporting its potential as a natural therapeutic agent for managing inflammation, oxidative stress, and wound healing.

This graphical abstract represents the main results of the study. It highlights the plant species under investigation: Lantana camara L.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), TGFB1 (transforming growth factor beta 1), ptges2.L (prostaglandin E synthase 2 L homeolog)
- **Chemicals:** nitric oxide (PubChem CID 145068)

## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}
- **Diseases:** Inflammation (MESH:D007249), Cytotoxicity (MESH:D064420)
- **Chemicals:** ROS (MESH:D017382), PGE2 (MESH:D015232), iridoid glycosides (MESH:D057889), Extract (-), flavonoids (MESH:D005419), NO (MESH:D009569), Lipid (MESH:D008055)
- **Species:** Lantana camara (species) [taxon 126435], Mus musculus (house mouse, species) [taxon 10090]

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12860513/full.md

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Source: https://tomesphere.com/paper/PMC12860513