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Journal of Chinese Pharmaceutical Sciences ›› 2025, Vol. 34 ›› Issue (1): 41-54.DOI: 10.5246/jcps.2025.01.004

• Original articles • Previous Articles     Next Articles

Unveiling the anti-inflammatory effects and mechanisms of LM49 in a carrageenan-induced acute inflammation model

Fan Yang1, Rui Li1, Wenting Liu1, Jian Sun2, Chengxiao Zhao1, Xiue Feng1, Qingshan Li1,2,*()   

  1. 1 School of Pharmaceutical Science, Medicinal Basic Research Innovation Center of Chronic Kidney Disease, Ministry of Education, Shanxi Medical University, Taiyuan 030001, Shanxi, China
    2 Shanxi Key Laboratory of Innovative Drug for the Treatment of Serious Diseases Basing on Chronic Inflammation, Shanxi University of Chinese Medicine, Taiyuan 030619, Shanxi, China
  • Received:2024-08-12 Revised:2024-09-20 Accepted:2024-11-07 Online:2025-02-20 Published:2025-02-20
  • Contact: Qingshan Li
  • Supported by:
    The National Natural Science Foundation of China (Grant No. 82003770), the National Science and Technology Major Project of China (Grant No. 2018ZX09711001-001-017), and the Key Research and Development Plan of Shanxi Province (Grant No. 202102130501005).

Abstract:

This study aimed to investigate the anti-inflammatory properties and underlying molecular mechanisms of 2,4ʹ,5ʹ-trihydroxyl-5,2ʹ-dibromo diphenylmethanone (LM49) using a carrageenan-induced paw edema model in mice, which serves as a well-established model for acute inflammation. Mice were randomly assigned into six groups, and acute inflammation was induced by injecting 1% carrageenan solution into the paw. To elucidate the anti-inflammatory effects and mechanisms of LM49, a comprehensive approach was employed, including pathology, transcriptomics, flow cytometry, RT-qPCR, Western blotting analysis, and molecular docking analysis. The results demonstrated that LM49 exerted a significant protective effect by reducing paw edema and lowering serum levels of pro-inflammatory cytokines IL-1β and TNF-α, while concurrently elevating anti-inflammatory cytokine IL-10 levels. Transcriptomic analysis identified 453 differentially expressed genes in the LM49-treated group. KEGG and GO enrichment analyses indicated that LM49 suppressed the NF-κB signaling pathway and modulated several other immune-inflammatory pathways. Molecular docking studies identified eight key targets of LM49 within the NF-κB signaling pathway. Furthermore, Western blotting analysis confirmed that LM49 inhibited the phosphorylation of p65 and IκB-α and downregulated the expression of MYD88 and TLR4 in mouse paw tissues. These findings provided a foundational understanding of the anti-inflammatory effects and molecular mechanisms of LM49, paving the way for further in-depth studies in this field.

Key words: Anti-inflammation, Transcriptomic, Molecular docking, Carrageenan, 2,4?,5?-Trihydroxyl-5,2?-dibromo diphenylmethanone

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