# Cedrol ameliorates inflammatory bowel disease via mitochondrial biogenesis, gut microbiota restoration, and intestinal barrier repair

**Authors:** Mo-Rong Xu, Chia-Hsin Lin, Chung-Hsuan Wang, Sheng-Yang Wang

PMC · DOI: 10.3389/fphar.2025.1619537 · Frontiers in Pharmacology · 2026-01-02

## TL;DR

Cedrol, a compound from wood essential oil, helps treat inflammatory bowel disease by improving mitochondrial function, gut bacteria balance, and intestinal barrier strength.

## Contribution

This study reveals cedrol's novel therapeutic potential for IBD through mitochondrial biogenesis and microbiota modulation.

## Key findings

- Cedrol increases ATP production and upregulates proteins like SIRT-1 and PGC-1α, enhancing mitochondrial function.
- Cedrol modulates gut microbiota by reducing harmful bacteria and increasing beneficial species like Blautia glucerasea.
- Cedrol elevates SCFA levels and tight junction protein expression, strengthening the intestinal barrier.

## Abstract

Inflammatory bowel disease (IBD) is a chronic inflammatory disorder of the gastrointestinal tract, primarily characterized by impaired intestinal barrier function. Enhancing mitochondrial ATP biosynthesis and restoring gut microbiota and metabolic balance may contribute to intestinal barrier repair and serve as a therapeutic strategy for IBD. Cedrol, the major component of Cunninghamia lanceolata var. konishii wood essential oil, is known for its anti-inflammatory and anti-bacterial properties. However, its effects on gut health remain unclear.

To evaluate the therapeutic effects of cedrol on inflammatory bowel disease (IBD), we assessed the expression of mitochondrial biogenesis and tight junction proteins using Western blotting. Additionally, we analyzed changes in gut microbiota and their metabolites, as well as colonic metabolites, through 16S rRNA gene sequencing, GC-MS, and 1H NMR analysis.

This study investigated the therapeutic potential of cedrol in an IBD model and found that it promotes colonic repair and enhances mitochondrial function by increasing ATP production and upregulating key proteins (SIRT-1, PGC-1α, Nrf2, p-AMPK/AMPK, TFAM). Furthermore, cedrol modulates gut microbiota balance by reducing Anaerostipes hadrus and Turicibacter sanguinis while increasing Blautia glucerasea and Anaerotaenia torta. It also elevates SCFA levels, supporting metabolic balance and the expression of tight junction protein expression, thereby strengthening the intestinal barrier and alleviating colitis.

In conclusion, cedrol effectively restores mitochondrial function, modulates gut microbiota and metabolic balances, and enhances intestinal barrier integrity, highlighting its potential as a therapeutic candidate for IBD.

## Linked entities

- **Proteins:** SIRT1 (sirtuin 1), PPARGC1A (PPARG coactivator 1 alpha), GABPA (GA binding protein transcription factor subunit alpha), TFAM (transcription factor A, mitochondrial)
- **Chemicals:** cedrol (PubChem CID 65575)
- **Diseases:** inflammatory bowel disease (MONDO:0005265), colitis (MONDO:0005292)
- **Species:** Cunninghamia lanceolata var. konishii (taxon 66170)

## Full-text entities

- **Diseases:** IBD (MESH:D015212), colitis (MESH:D003092), bacterial (MESH:D001424), inflammatory (MESH:D007249)
- **Chemicals:** 1H (-), SCFA (MESH:D005232), Cedrol (MESH:C078669), ATP (MESH:D000255)
- **Species:** Blautia glucerasea (species) [taxon 536633], Anaerotaenia torta (species) [taxon 433293], Anaerostipes hadrus (species) [taxon 649756], Turicibacter sanguinis (species) [taxon 154288]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12808353/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12808353/full.md

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Source: https://tomesphere.com/paper/PMC12808353