Abstract

Toll-like receptor 4 (TLR4) and matrix metalloproteinase-9 (MMP-9) are known to play important roles in inflammatory diseases such as arteriosclerosis and plaque instability. The purpose of this study was to perform the effect of 4-O-carboxymethylascochlorin (AS-6) on MMP-9 expression in lipopolysaccharide (LPS)-induced murine macrophages and signaling pathway involved in its anti-inflammatory effect. Effect of AS-6 on MAPK/NF-κB/TLR4 signaling pathway in LPS-activated murine macrophages was examined using ELISA, Western blotting, reverse transcription polymerase chain reaction (RT-PCR) and fluorescence immunoassay. MMP-9 enzyme activity was examined by gelatin zymography. AS-6 significantly suppressed MMP-9 and MAPK/NF-κB expression levels in LPS-stimulated murine macrophages. Expression levels of inducible nitric oxide synthase (iNOS), COX2, MMP-9, JNK, ERK, p38 phosphorylation, and NF-κB stimulated by LPS were also decreased by AS-6. Moreover, AS-6 suppressed TLR4 expression and dysregulated LPS-induced activators of transcription signaling pathway. The results of this study showed that AS-6 can inhibit LPS-stimulated inflammatory response by suppressing TLR4/MAPK/NF-κB signals, suggesting that AS-6 can be used to induce the stability of atherosclerotic plaque and prevent inflammatory diseases in an in vitro model.

Highlights

  • Inflammation is the body’s defensive response to a stimulus (Klasing, 1991)

  • Our results indicated that various concentrations of AS-6 decreased Matrix metallopeptidase 9 (MMP-9) expression in LPS-activated murine macrophages

  • Production of Nitric Oxide (NO) and prostaglandin E2 (PGE2) as major mediators of inflammatory response was inhibited by AS-6 (Figure 2)

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Summary

Introduction

Inflammation is the body’s defensive response to a stimulus (Klasing, 1991). While general inflammation leads to tissue protection and injury regeneration in response to injury and infection, chronic inflammation usually leads to loss of immune system, resulting in tissue damage and the occurrence of various diseases. Inflammation is linked to various chronic diseases such as vascular dysfunction, heart diseases, cancers, neurological disorders, obesity, diabetes, and atherosclerotic plaques (Jayson, 1989). It is prominently marked in vulnerable areas of atherosclerotic plaque (Hernandez-Barrantes et al, 2002; Murphy et al, 2002). MMP-9 is prominently marked in the vulnerable areas of the atherosclerotic plaque (Kalela et al, 2000; Arihiro et al, 2001). Pro-inflammatory cytokine and MMP-9 are important factors that provide plaque the decomposition of ECM. MMP is known to be the main cause of atherosclerosis

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