REVIEW article
Front. Pharmacol.
Sec. Respiratory Pharmacology
This article is part of the Research TopicRedox Pharmacology in Pulmonary Disease: Targeting Oxidative Stress, Inflammation, and Environmental HazardView all articles
Polydatin in Respiratory Diseases: Multi-Target Mechanisms and Therapeutic Potential
Provisionally accepted- Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, China
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Respiratory diseases constitute a heterogeneous group of disorders that primarily involve the lungs. Driven by worsening air pollution, tobacco use, occupational exposures, the COVID-19 pandemic, and population aging, they show persistently high incidence with rising mortality and disability, posing a major global public-health challenge. Current pharmacotherapies—principally antibiotics, glucocorticoids, β2-adrenoceptor agonists, and antiviral agents—yield only limited benefit and are constrained by adverse reactions such as gastrointestinal disturbances and hepatorenal toxicity, alongside the escalating problem of drug resistance. The development of safer and more effective therapeutics is therefore of considerable clinical and socioeconomic importance. Plant-derived natural products have attracted increasing interest in the management of respiratory diseases. Polydatin (resveratrol-3-O-β-D-glucoside; also known as piceid; PD) is a stilbenoid polyphenol of plant origin that is widely distributed in Polygonum cuspidatum (Japanese knotweed), Polygonum multiflorum, grapes, peanuts, mulberries, blueberries, and rhubarb. Accumulating evidence indicates that PD exerts anti-inflammatory, antioxidant, antimicrobial, immunomodulatory, and metabolic-regulatory activities and shows potential therapeutic value in pulmonary fibrosis, acute lung injury/acute respiratory distress syndrome, pneumonia, lung cancer, and asthma. This review provides a comprehensive synthesis of the multi-target and multi-pathway mechanisms by which PD acts against respiratory diseases, offering a mechanistic rationale and evidence base to support its clinical development.
Keywords: molecular targets, Pharmacological mechanism, Polydatin, Respiratory diseases, Signaling Pathways
Received: 23 Nov 2025; Accepted: 05 Jan 2026.
Copyright: © 2026 Wan, Liu, chen, Xu, Kang, Yu, Wang, Zhao, Li, Wu, Liu and Xu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Liangji Liu
Xuemei Xu
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