# Antifibrotic Effects of Thymus syriacus Essential Oil in Bleomycin-Induced Pulmonary Fibrosis via Suppression of the TGF-β1/Smad2 Axis

**Authors:** Pınar Aksoy, Önder Yumrutaş, Muhittin Doğan, Pınar Yumrutaş, Mehmet Sökücü, Mustafa Pehlivan

PMC · DOI: 10.3390/ijms27031401 · International Journal of Molecular Sciences · 2026-01-30

## TL;DR

This study shows that Thymus syriacus essential oil reduces lung fibrosis by targeting the TGF-β1/Smad2 pathway and reducing inflammation and oxidative stress.

## Contribution

The study demonstrates the antifibrotic effects of Thymus syriacus essential oil via suppression of the TGF-β1/Smad2 axis in a bleomycin-induced model.

## Key findings

- TS significantly reduced TGF-β1, SMAD2, COL1, α-SMA, TNF-α, ROS, and MDA levels compared to the bleomycin group.
- Thymol, p-cymene, and carvacrol were identified as major constituents of TS.
- TS treatment attenuated pulmonary fibrosis and showed no significant toxicity.

## Abstract

Background: Pulmonary fibrosis (PF) is an irreversible interstitial lung disease in which the TGF-β/SMAD signaling pathway plays a critical role in its pathogenesis. Due to the anti-inflammatory and antioxidant properties of Thymus species, it is hypothesized that they may suppress pulmonary fibrosis by modulating the TGF-β/SMAD pathway. This study aimed to investigate the potential antifibrotic effects of Thymus syriacus essential oil (TS) on the TGF-β/SMAD pathway in bleomycin-induced PF. Methods: PF was induced with bleomycin, and TS was administered at concentrations of 50 and 100 mg/mL for 28 days. mRNA and protein levels of TGF-β1, SMAD2, COL1, and α-SMA in lung tissues isolated were analyzed using real-time PCR and ELISA. TNF-α levels in BALF were measured by ELISA. ROS and MDA levels in lung issues were determined using 2,7-DHCFDA and TBARS tests, respectively. Histopathological evaluation was performed using Hematoxylin–Eosin and Masson’s trichrome staining. Blood samples were analyzed for kidney, liver, and cardiac toxicity markers. The chemical composition of TS was determined by GC–MS. Results: TS significantly reduced levels of TGF-β1, SMAD2, COL1, α-SMA, TNF-α, ROS and MDA compared to the BLM group. PF alterations were markedly attenuated by TS treatment. Thymol, p-cymene and carvacrol were identified as major constituents of TS. Conclusion: Overall, TS alleviates pulmonary fibrosis by suppressing the TGF-β/SMAD2 signaling pathway.

## Linked entities

- **Proteins:** TGFB1 (transforming growth factor beta 1), SMAD2 (SMAD family member 2), COL1 (CONSTANS-like 1), ACTA1 (actin alpha 1, skeletal muscle), TNF (tumor necrosis factor)
- **Chemicals:** bleomycin (PubChem CID 5360373), thymol (PubChem CID 6989), p-cymene (PubChem CID 7463), carvacrol (PubChem CID 10364), MDA (PubChem CID 1614)
- **Diseases:** pulmonary fibrosis (MONDO:0002771)
- **Species:** Thymus syriacus (taxon 1885668)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}, SMAD2 (SMAD family member 2) [NCBI Gene 4087] {aka CHTD8, JV18, JV18-1, LDS6, MADH2, MADR2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** interstitial lung disease (MESH:D017563), PF (MESH:D011658), , liver, and cardiac toxicity (MESH:D066126), inflammatory (MESH:D007249)
- **Chemicals:** p-cymene (MESH:C007210), carvacrol (MESH:C073316), 2,7-DHCFDA (-), TBARS (MESH:D017392), BLM (MESH:D001761), Thymol (MESH:D013943), Hematoxylin (MESH:D006416), MDA (MESH:D015104), TS (MESH:D014316)

## Full text

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## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12898269/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12898269/full.md

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Source: https://tomesphere.com/paper/PMC12898269