Anti-inflammatory effects of Rhus javanica ethanol extract for pulmonary and colonic disorders.

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Tác giả: Jae Youl Cho, Ziliang He, Lei Huang, Won Young Jang, Yerkyesh Khamit, Eun Sil Kim, Ji Won Kim, Seung Hyun Kim, Byoung-Hee Lee, Jaeyoun Lee, Canglang Mou, Fan Qu, Sun Moo Rhee, Youn Kyoung Son, Jinghan Su, Fangfang Wang, Yuhao Wang, Ji Hye Yoon, Long You

Ngôn ngữ: eng

Ký hiệu phân loại: 969.6 +Seychelles

Thông tin xuất bản: Germany : Phytomedicine : international journal of phytotherapy and phytopharmacology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 691443

BACKGROUND: Rhus javanica is a traditional medicinal herb widespread in East Asia, including Korea, China, and Japan. Valued for its antidiarrheal, bactericidal, and anti-inflammatory properties, it epitomizes the synergy of traditional wisdom and natural benefits. PURPOSE: This study aimed to investigate the anti-inflammatory properties of Rhus javanica ethanol extract (Rj-EE) in both in vitro and in vivo models, elucidate the underlying mechanisms, and provide a theoretical foundation for its potential use as a natural therapeutic option for clinical colitis and lung diseases. STUDY DESIGN: RAW264.7 cells, peritoneal macrophages, HEK293T cells, and mouse models of acute lung injury and acute ulcerative colitis were used to evaluate the anti-inflammatory activity of Rj-EE. METHODS: In this study, the phytochemical constituents of Rj-EE were identified by GC-MS and LC-MS. Inflammatory targets were sourced from GeneCards and Swiss Target Prediction databases. Gene ontology and KEGG analyses revealed Rj-EE's anti-inflammatory mechanisms. Nitric oxide (NO) production and cell viability were assessed with Griess and MTT assays, respectively. Inflammatory cytokines were measured by RT-PCR, transcription factor activity by luciferase assays, and protein expression through Western blotting. Overexpression and CETSA assays were conducted in HEK293T cells. In vivo model animals with lipopolysaccharide-induced acute lung injury and dextran sulfate sodium-induced acute ulcerative colitis were treated with Rj-EE and then assessed by RT-PCR, hematoxylin and eosin (H&E), cytokine analysis via an enzyme-linked immunosorbent assay, and Western blotting. RESULTS: KEGG analysis identified the NF-κB pathway as key to Rj-EE's anti-inflammatory effects, with Src as a central target. Molecular docking showed strong binding between Rj-EE's active components and key genes. In vitro, Rj-EE reduced NO production and inflammatory mRNA markers, and inhibited MyD88- and TRIF-induced NF-κB and AP-1 activity. It also targeted Src and Syk. In vivo, Rj-EE alleviated colitis and lung injury. CONCLUSION: Overall, Our findings lay a foundation for further research into Rj-EE's molecular anti-inflammatory mechanisms and suggest that Rhus javanica could be explored as a potential anti-inflammatory agent targeting Src and Syk for conditions like lung injury and colitis.
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