4.4 Article

Curcumin reduces the expression of interleukin 1 beta and the production of interleukin 6 and tumor necrosis factor alpha by M1 macrophages from patients with Behcet's disease

Journal

IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY
Volume 40, Issue 4, Pages 297-302

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/08923973.2018.1474921

Keywords

Behcet's disease; curcumin; interleukin 1 beta; interleukin 6; M1 macrophage; tumor necrosis factor alpha

Funding

  1. Tehran University of Medical Sciences and health services [94-01-41-28377]

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Objective: Behcet's disease (BD) is an auto-inflammatory disorder. Curcumin as a bio-active agent has anti-inflammatory properties. Effects of curcumin on the pathogenesis of BD are still not clear. In this study, we investigated the effect of curcumin on the inflammatory cytokines expression and production in M1 macrophages from BD patients compared with healthy controls. Methods: Monocytes were collected from 10 healthy controls and 20 active BD patients, differentiated to macrophages by macrophage-colony stimulating factor for 7d. Macrophages were then treated with interferon gamma, lipopolysaccharide, and curcumin (10 or 30 mu g/ml) for 24h. Analysis of tumor necrosis factor-alpha (TNF), interleukin 1 beta (IL-1 beta), and IL-6 mRNA expression and protein production was performed using SYBR Green qPCR and ELISA method. Results: Treatment with 30 mu g/ml curcumin significantly down-regulated mRNA expression of IL-1 beta (p<.05) and protein production of IL-6 (p<.05) in M1 macrophages from BD patients but not in M1 macrophage from controls. Treatment with 30 mu g/ml curcumin also significantly diminishes the protein production of TNF in BD patients (p<.01) and healthy controls (p<.05) M1 macrophages. Conclusions: We demonstrated that curcumin can inhibit the expression and production of inflammatory cytokines in M1 macrophages from BD patients. Our results suggest that curcumin can modulate inflammatory signaling more specifically in macrophages from BD patients than healthy macrophages.

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