Eckmaxol Isolated from Ecklonia maxima Attenuates Particulate-Matter-Induced Inflammation in MH-S Lung Macrophage

Mar Drugs. 2022 Dec 7;20(12):766. doi: 10.3390/md20120766.

Abstract

Airborne particulate matter (PM) originating from industrial processes is a major threat to the environment and health in East Asia. PM can cause asthma, collateral lung tissue damage, oxidative stress, allergic reactions, and inflammation. The present study was conducted to evaluate the protective effect of eckmaxol, a phlorotannin isolated from Ecklonia maxima, against PM-induced inflammation in MH-S macrophage cells. It was found that PM induced inflammation in MH-S lung macrophages, which was inhibited by eckmaxol treatment in a dose-dependent manner (21.0−84.12 µM). Eckmaxol attenuated the expression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) in PM-induced lung macrophages. Subsequently, nitric oxide (NO), prostaglandin E-2 (PGE-2), and pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α) were downregulated. PM stimulated inflammation in MH-S lung macrophages by activating Toll-like receptors (TLRs), nuclear factor-kappa B (NF-κB), and mitogen-activated protein kinase (MAPK) pathways. Eckmaxol exhibited anti-inflammatory properties by suppressing the activation of TLRs, downstream signaling of NF-κB (p50 and p65), and MAPK pathways, including c-Jun N-terminal kinase (JNK) and p38. These findings suggest that eckmaxol may offer substantial therapeutic potential in the treatment of inflammatory diseases.

Keywords: Ecklonia maxima; anti-inflammation; bioactive compound; chronic diseases; eckmaxol; lung macrophage; particulate matter.

MeSH terms

  • Cyclooxygenase 2 / metabolism
  • Humans
  • Inflammation* / chemically induced
  • Inflammation* / drug therapy
  • Lung* / drug effects
  • Lung* / pathology
  • Macrophages* / drug effects
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Particulate Matter* / toxicity
  • Phaeophyceae* / chemistry
  • Pneumonia* / chemically induced
  • Pneumonia* / drug therapy
  • Polyphenols* / chemistry
  • Polyphenols* / pharmacology
  • Polyphenols* / therapeutic use
  • Toll-Like Receptors / metabolism

Substances

  • Cyclooxygenase 2
  • Mitogen-Activated Protein Kinases
  • NF-kappa B
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Particulate Matter
  • Toll-Like Receptors
  • Polyphenols

Grants and funding

This research was supported by the 2022 scientific promotion program funded by Jeju National University.