Abstract

To investigate the effect of acylated ghrelin on the activation of TLR4/NF-κB signaling pathway induced by palmitic acid in human monocyte-derived (THP-1) macrophages, THP-1 macrophages were cultured for 12 h by palmitic acid with various concentrations. The THP-1 macrophages was pretreated by acylated ghrelin at different doses for 4 h before cultivated by palmitic acid (200 μmol/L) for 12 h. We observed the level of TLR4, NF-κB p65 phosphorylation in THP-1 macrophages and TNF-α, IL-1β in culture supernatant. TLR4 mRNA was measured by real-time PCR. TLR4 protein and NF-κB p65 phosphorylation was measured by western blotting. The expression of TNF-α and IL-1β was detected by ELISA. Compared to the THP-1 macrophages without palmitic acid, the level of TLR4 mRNA protein and NF-κB p65 phosphorylation and the expression of TNF-α and IL-1β increased after treatment by palmitic acid in a dose-dependent fashion (P < 0.05). Compared to the THP-1 macrophages with palmitic acid (200 μmol/L), the level of the pervious substances decreased after preadministration by acylated ghrelin in a dose-dependent fashion. So, we make a conclusion that acylated ghrelin can regulate the activation of TLR4/NF-κB signaling pathway and inhibit the release of inflammatory cytokines in THP-1 macrophages which are stimulated by palmitic acid in a dose-dependent fashion.

Highlights

  • Obesity is a chronic disease that is associated with lowgrade inflammation [1,2,3]

  • THP-1 macrophages were incubated with different concentrations of palmitic acid (100 μmol/L, 200 μmol/L, and 500 μmol/L) and 10 ng/mL LPS for 12 hours

  • We chose to incubate THP-1 macrophages with palmitic acid, which is a type of saturated fatty acid

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Summary

Introduction

Obesity can induce changes in metabolism and gene expression in adipocytes, thereby enhancing lipolysis and releasing proinflammatory free fatty acids (FFAs) and cytokines (such as monocyte chemotactic protein-1 (MCP-1) and tumor necrosis factor-alpha (TNFα)), which are able to recruit and activate macrophages to produce high levels of proinflammatory mediators (such as TNF-α, interleukin-1 beta (IL-1β), and resistin). These proinflammatory factors can promote an insulin-resistant state in adipocytes and form a positive feedback loop. Obesity has been shown to be associated with the activation of the innate immunity pathway and inflammatory response, as well as an impaired insulin signaling pathway and insulin resistance [5,6,7,8,9,10]

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