Baicalin Ameliorates Inflammatory Response in a Mouse Model of Rhinosinusitis via Regulating the Treg/Th17 Balance

Author:

Yang Ming1,Zhu Xiaoyan1,Fu Feida1,Guo Qinghua1,Zhu Xiaopu2,Xu Yang3,Yan Xiaotian4,He Xinya1,Wang Xu1ORCID

Affiliation:

1. Department of Otorhinolaryngology, Nanjing Integrated Traditional Chinese and Western Medicine Hospital, Nanjing, China

2. Department of Otorhinolaryngology, Suzhou Integrated Chinese and Western Medicine Hospital, Suzhou, China

3. Department of Otorhinolaryngology, Wuxi Chinese Medicine Hospital, Wuxi, China

4. Department of Otorhinolaryngology, Changzhou Chinese Medicine Hospital, Changzhou, China

Abstract

Objective: Rhinosinusitis is a global health problem affecting millions of people around the world. Baicalin is a bioactive compound isolated from medicinal plant Scutellaria baicalensis Georgi. The present study aims to investigate potential effects of baicalin on clinicopathological changes in nasal/sinus mucosa in a mouse model. Methods: A mouse model of sinonasal inflammation induced by high dose of ovalbumin was applied to evaluate effects of baicalin. Rhinosinusitis symptoms, histopathological features, levels of histamine, immunoglobulin E (IgE), IL-17A, IL-10, and balance of regulatory T cell (Treg)/T-helper 17 (Th17) responses were examined. Results: Baicalin significantly relieved rhinosinusitis symptoms in mice, reduced histopathological changes, and suppressed serum levels of histamine and IgE in a dose-dependent manner. In lymphocytes of mice, baicalin modulated balance of Treg/Th17 proportions by attenuating Th17 cells and enhancing Treg cells, respectively. The serum IL-17A was decreased and IL-10 was increased in mice treated by baicalin. In addition, baicalin promoted levels of Smad protein 3 (p-Smad3) and forkhead box P3 (FOXP3) to promote Treg cells while suppressed levels of p-Stat3 and retineic-acid-receptor-related orphan nuclear receptor γt ( RORγt) to inhibit Th17 cells. Conclusions: These data demonstrate that baicalin effectively ameliorates sinonasal inflammation in a mouse model by recovering the immunological balance of Treg/Th17 responses. Our finding highlights the potential value of baicalin for the treatment of rhinosinusitis.

Funder

Nanjing Science and technology development projects

Publisher

SAGE Publications

Subject

Otorhinolaryngology

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