Fici hirtae radix alleviates influenza A virus-induced acute lung injury via TLR4-PI3K-AKT/p38 MAPK-NF-κB signaling pathway.

ETHNOPHARMACOLOGICAL RELEVANCE: Fici hirtae radix (FHR), documented in the classical Chinese medicinal text "The Characteristics, Uses and Preparation of Medicinal Herbs", has demonstrated clinical efficacy in alleviating respiratory infections. However, its anti-influenza effects and mechanisms remain unclear, dramatically restricting its product development.

AIM OF THE STUDY: This study aimed to explore the protective effects of FHR against acute lung injury (ALI) and its underlying mechanisms.

MATERIALS AND

METHODS

The influenza virus A pdm 2009 (H1N1) induced ALI mouse model was used to investigate the anti-influenza effects of FHR extracts. Survival index, lung index, histopathological analysis of pulmonary tissue were assessed. Meanwhile, white blood cell (WBC) counts (including total WBCs, neutrophils, monocytes, and lymphocytes) were measured in both blood and bronchoalveolar lavage fluid (BALF), along with cytokine levels in BALF. The phytochemical information of FHR extracts in vitro and in vivo was analyzed via ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q/TOF MS). Based on the in vivo prototypes of FHR, network pharmacology was used to predict its anti-influenza targets and mechanism pathways. Further, Western blotting was used for mechanism validation.

RESULTS

FHR (20 g crude drug/kg/day) significantly improved survival rates, reduced lung index, and suppressed viral NP expression in lung tissue. FHR treatment also markedly alleviated pulmonary inflammation by suppressing the H1N1-induced over-recruitment of neutrophils and monocytes, and by rebalancing cytokine levels in BALF-specifically, downregulating IL-6, IL-1β, IL-17A, and IFN-β while upregulating IL-10. Meanwhile, phytochemical profiling results revealed that a total of 157 compounds (including flavonoids, coumarins and organic acids, etc.) were identified in FHR and 17 prototypes (psoralen and apigenin, etc.) were identified in plasma. TLR4-PI3K-AKT/p38 MAPK-NF-κB signaling pathway, a potential key pathway for FHR against influenza, was predicted by network pharmacology and validated by Western blot in lungs, effectively suppressing influenza virus-induced ALI.

CONCLUSIONS

FHR exerts anti-influenza effects by regulating the TLR4-PI3K-AKT/p38 MAPK-NF-κB signaling pathway.