Exploring the total flavones of Abelmoschus manihot against IAV-induced lung inflammation by network pharmacology

BMC Complementary Medicine and Therapies

Zihao Liang¹  Huihui Zhou¹  Junfeng Zhang¹  Yanan Gao¹  Nianyin Lv¹  Liyun Shi²  Jinjun Shan³ 

[1] School of Medicine, Nanjing University of Chinese Medicine, 210046, Nanjing, China;School of Medicine, Nanjing University of Chinese Medicine, 210046, Nanjing, China;School of Medicine, Zhejiang Shuren University, 310015, Hangzhou, Zhejiang, China;The First School of Clinical Medicine, The Affiliated Hospital of Nanjing University of Chinese Medicine, 210029, Nanjing, China;

关键词: Network pharmacology;    IAV;    TFA;    Anti-inflammation;    Anti-virus;   

DOI  :  10.1186/s12906-022-03509-0

来源: Springer

【 摘 要 】

BackgroundAbelmoschus manihot (L.) Medicus (AM) is a medicinal plant with various biological activities, including anti-inflammatory, antioxidant, antiviral and immunomodulatory. Previous studies have identified total flavones as the primary bioactive ingredient of AM (termed TFA). However, its role and mechanism in counteracting Influenza A virus (IAV) infection are yet to be explored. Therefore, the study aims to study the antiviral and anti-inflammatory effects of TFA on IAV in vitro and in vivo.MethodsA network pharmacology-based approach was applied to identify the antiviral mechanism of TFA against IAV. For the mechanism validation, the cytopathic effect reduction assay evaluated the antiviral activity of TFA in vitro. Meanwhile, the mice were intranasally infected with IAV to induce lung infection. The antiviral effect of TFA was observed in vivo. Further investigation whether the reprogramming microbiome in the TFA treatment group affected antiviral, we conducted a microbial-transfer study with co-housing experiments.ResultsBy applying the network pharmacology-based methods (PPI, GO, and KEGG), we identified 167 potential targets of TFA action, among which 62 targets were related to IAV pathogenesis. A core network containing the pro-inflammatory TNFα, IL-6, IL-1β, MAPKs, and RIG-I receptor signaling pathway was further confirmed as the crucial targets for anti-influenza efficacy of TFA. We demonstrate that TFA provided profound protection against pulmonary IAV infection, which alleviated inflammatory responses, decreased MAPK signaling pathway and expedited viral eradiation.ConclusionsOur study unveils a pivotal role for TFA in controlling viral infection and dampening pathology, making it a promising strategy for treating IAV-induced pneumonia.

【 授权许可】

CC BY