| Literature DB >> 25929447 |
Souvik Sarkar1, Asim A Siddiqui1, Somnath Mazumder1, Rudranil De1, Shubhra J Saha1, Chinmoy Banerjee1, Mohd S Iqbal1, Susanta Adhikari2, Athar Alam1, Siddhartha Roy3, Uday Bandyopadhyay1.
Abstract
Ellagic acid (EA), a phenolic lactone, inhibited tautomerase activity of human macrophage migration inhibitory factor (MIF) noncompetitively (Ki = 1.97 ± 0.7 μM). The binding of EA to MIF was determined by following the quenching of tryptophan fluorescence. We synthesized several EA derivatives, and their structure-activity relationship studies indicated that the planar conjugated lactone moiety of EA was essential for MIF inhibition. MIF induces nuclear translocation of NF-κB and chemotaxis of peripheral blood mononuclear cells (PBMCs) to promote inflammation. We were interested in evaluating the effect of EA on nuclear translocation of NF-κB and chemotactic activity in human PBMCs in the presence of MIF. The results showed that EA inhibited MIF-induced NF-κB nuclear translocation in PBMCs, as evident from confocal immunofluorescence microscopic data. EA also inhibited MIF-mediated chemotaxis of PBMCs. Thus, we report MIF-inhibitory activity of EA and inhibition of MIF-mediated proinflammatory responses in PBMCs by EA.Entities:
Keywords: chemotaxis; ellagic acid; gallic acid; inflammation; macrophage migration inhibitory factor; tautomerase activity
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Year: 2015 PMID: 25929447 DOI: 10.1021/acs.jafc.5b00921
Source DB: PubMed Journal: J Agric Food Chem ISSN: 0021-8561 Impact factor: 5.279