Publication | Open Access
Quercetin Suppresses MIP-1α–Induced Adipose Inflammation by Downregulating Its Receptors CCR1/CCR5 and Inhibiting Inflammatory Signaling
37
Citations
25
References
2013
Year
ImmunologyOxidative StressObesity-induced InflammationInflammationMetabolic SyndromeObesityMip-1α ReleaseMetabolic SignalingCell SignalingMip-1α–induced Adipose InflammationMolecular SignalingHealth SciencesAdipose TissueReceptors Ccr1/ccr5Chronic InflammationVascular BiologyPharmacologyCell BiologyInflammatory DiseaseCytokineAnti-inflammatoryPhysiologyMetabolic RegulationMedicineInhibiting Inflammatory
Obesity-induced inflammation is characterized by recruitment of adipose tissue macrophages that release inflammatory cytokines and chemokines. MIP-1α (macrophage inflammatory protein 1α)/CCL3, a CC chemokine, induces monocyte/macrophage infiltration and thus is implicated in obesity-induced adipose inflammation. Quercetin has been shown to modulate obesity-induced inflammation, but the mechanism of its action remains unclear. Here we demonstrate that quercetin decreases MIP-1α release from adipocytes and macrophages and from cocultured adipocytes/macrophages; it also opposes MIP-1α-induced macrophage infiltration and activation. The inhibitory action of quercetin on the MIP-1α-induced inflammatory responses of macrophages is mediated by downregulation of CCR1/CCR5, and inhibition of activation of JNK, p38 mitogen-activated-protein kinase (MAPK), and IKK as well as IκBα degradation. These findings suggest that quercetin may be a useful agent against obesity-induced adipose tissue inflammation.
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