# Medicinal plants and compounds for chronic bronchitis treatment: efficacy and action mechanisms

**Authors:** Wei Ding, Danni Chen, Jiawang Li, Yan Wang, Xiangyun Chen, Yihe Xu, Zhen Yang, Zhenhong Liu, Hongxia Zhao

PMC · DOI: 10.3389/fphar.2025.1674079 · 2025-10-29

## TL;DR

This review explores how medicinal plants and compounds can treat chronic bronchitis by targeting inflammation and other key symptoms.

## Contribution

The first comprehensive synthesis of experimentally verified efficacy and mechanisms of medicinal plants and compounds in chronic bronchitis treatment.

## Key findings

- 13 medicinal plants and 19 compounds showed anti-inflammatory activity against chronic bronchitis.
- Ursolic acid emerged as the most promising candidate for clinical development.
- Natural agents demonstrated antioxidant, anti-mucus, and bronchodilatory effects through multiple molecular pathways.

## Abstract

Chronic bronchitis (CB) is a common yet heterogeneous condition characterized by persistent inflammation, oxidative stress, airway hyperresponsiveness, and mucus hypersecretion. As an early stage of various severe pulmonary diseases, current therapeutic strategies remain unsatisfactory. Substantial evidence indicates that medicinal plants and compounds hold potential for treating inflammatory lung disorders. This study aims to consolidate recent and reliable evidence concerning the multi-targeted roles and underlying molecular mechanisms of these natural products in the treatment of CB.

This systematic review followed a prospectively registered protocol (PROSPERO ID: CRD42024588912). A comprehensive literature search encompassed multiple electronic databases, including PubMed, Scopus, Embase, Web of Science, VIP, Wan-fang, SinoMed, and the China National Knowledge Infrastructure Study selection strictly adhered to the PICOS principles to systematically identify medicinal plants and compounds with therapeutic potential against Chronic bronchitis.

The results identified 13 medicinal plants and 19 compounds that exhibited anti-inflammatory activity. Additionally, 8 plants and 12 compounds demonstrated further therapeutic effects, including antioxidant, anti-mucus, and potential bronchodilatory activities. The underlying mechanisms primarily involved the NF-κB, PI3K/AKT/mTOR, TLR4, MAPK, and Nrf2 pathways. Ursolic acid emerged as the most promising clinical candidate.

This review represents the first comprehensive synthesis of experimentally verified efficacy and mechanisms associated with medicinal plants and compounds in CB treatment. Preclinical animal studies have confirmed the therapeutic benefits of these natural agents in alleviating CB symptoms, establishing a solid foundation for novel drug development and underscoring their considerable translational potential.

## Linked entities

- **Proteins:** NFKB1 (nuclear factor kappa B subunit 1), TLR4 (toll like receptor 4), MAPK (mitogen activated kinase-like protein), GABPA (GA binding protein transcription factor subunit alpha)
- **Chemicals:** Ursolic acid (PubChem CID 64945)
- **Diseases:** Chronic bronchitis (MONDO:0003781)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}
- **Diseases:** inflammation (MESH:D007249), pulmonary diseases (MESH:D008171), inflammatory lung disorders (MESH:D016726), CB (MESH:D029481)
- **Chemicals:** Ursolic acid (MESH:C005466)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12616378/full.md

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Source: https://tomesphere.com/paper/PMC12616378