Abstract

Catechin, a flavonol belonging to the flavonoid group of polyphenols is present in many plant foods. The present study was done to evaluate the effect of catechin on various inflammatory mediators using lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. The effect of catechin on total cyclooxygenase (COX) activity, 5-lipoxygenase (5-LOX), myeloperoxidase, nitrite and inducible nitric oxide synthase (iNOS) level, secretion of tumor necrosis factor-α (TNF-α) and interleukin-10 (IL-10) were assessed in LPS-stimulated RAW 264.7 cells. The expression of COX-2, iNOS, TNF-α, nuclear factor-ĸB (NF-κB) and p38 mitogen-activated protein kinase (MAPK) genes were also investigated. The effect was further analyzed using human PBMCs by assessing the level of TNF-α and IL-10. The study demonstrated that the inflammatory mediators such as COX, 5-LOX, nitrite, iNOS, and TNF-α were significantly inhibited by catechin in a concentration-dependent manner whereas IL-10 production was up-regulated in RAW 264.7 cells. Moreover, catechin down-regulated the mRNA level expression of COX-2, iNOS, TNF-α, NF-κB and p38 MAPK. The current study ratifies the beneficial effect of catechin as a dietary component in plant foods to provide protection against inflammatory diseases.

Highlights

  • Inflammation is an invasive phenomenon that functions during severe changes of homeostasis, for instance, injury, infection, and contaminant exposure (Ashley et al, 2012)

  • The study demonstrated that the inflammatory mediators such as COX, 5-LOX, nitrite, inducible nitric oxide synthase (iNOS), and tumour necrosis factor-α (TNF-α) were significantly inhibited by catechin in a dose-dependent manner whereas IL-10 production was up-regulated in RAW 264.7 cells

  • We have examined the effect of catechin on various inflammatory mediators such as COX, 5-LOX, nitrite, iNOS, myeloperoxidase (MPO), TNF-α and IL-10 in LPS-stimulated RAW 264.7 macrophages and on the production of TNF-α and IL-10 in human peripheral blood mononuclear cells (PBMCs)

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Summary

Introduction

Inflammation is an invasive phenomenon that functions during severe changes of homeostasis, for instance, injury, infection, and contaminant exposure (Ashley et al, 2012). Catechin was described as a histidine decarboxylase inhibitor, preventing the histidine to histamine conversion in stress ulcer condition (Reimann et al, 1977) This phytochemical inhibits monoamine oxidase B (MAO-B) activity and was found to be against oxidative neurodegeneration occurring in Alzheimer’s and Parkinson’s diseases (Hou et al, 2005). We have examined the effect of catechin on various inflammatory mediators such as COX, 5-LOX, nitrite, iNOS, myeloperoxidase (MPO), TNF-α and IL-10 in LPS-stimulated RAW 264.7 macrophages and on the production of TNF-α and IL-10 in human peripheral blood mononuclear cells (PBMCs)

Cell culture
Drug treatment
Preparation of cell lysate for assays
Effect of catechin on cell viability
Effect of catechin on myeloperoxidase activity
Effect of catechin on nitrite level
2.2.10. Effect of catechin on cytokine secretion
Effect of catechin on cytokine secretion
Statistical analysis
Results
Effect of catechin on 5-LOX activity
Effect of catechin on the viability of human PBMCs
3.10. Effect of catechin on cytokine secretion by human PBMCs
Discussion
Conclusion
Full Text
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