| Literature DB >> 25466017 |
Gui-Yun Cao1, Wei Xu1, Xiu-Wei Yang2, Frank J Gonzalez3, Fei Li4.
Abstract
Five new 8-O-4' type neolignans, named myrifralignan A-E (1-5), together with five known analogues (6-10), were isolated from the seeds of Myristica fragrans Houtt. Their chemical structures were determined using several spectroscopic methods. Compounds 3-10 exhibited potent inhibitory activity against the production of nitric oxide (NO) in the RAW264.7 cell line stimulated by lipopolysaccaride. Myrislignan (7) and machilin D (10) were the most potent inhibitors of NO production amongst these compounds. The IC50 values of myrislignan and machilin D were 21.2 and 18.5 μM. And, their inhibitory activity was more than L-N(6)-(1-iminoethyl)-lysine, a selective inhibitor of inducible nitric oxide synthase (IC50=27.1 μM). Furthermore, real-time PCR analysis revealed that these neolignans could significantly suppress the expression of inducible nitric oxide synthase mRNA. These results demonstrated that the 8-O-4' type neolignans are promising candidates as anti-inflammatory agents.Entities:
Keywords: Inhibition; Myristica fragrans; Neolignans; Nitric oxide; iNOS mRNA
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Year: 2014 PMID: 25466017 PMCID: PMC6338084 DOI: 10.1016/j.foodchem.2014.09.170
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514