| Literature DB >> 34227156 |
Lei Dong1, Ling Fang2, Xinxiang Dai3, Jia Zhang1, Jia Wang1, Pei Xu1.
Abstract
Periodontitis is a serious global concern. Therefore, in the present study, we intend to synthesize novel valproic-acid pyrazole conjugates as a novel agent against periodontitis. The molecules were developed in a facile synthetic route and obtained in excellent yields. The entire set of molecules were screened for antibacterial activity against a battery of micro-organisms responsible for periodontitis such as P. gingivalis, P. intermedia, F. nucleatum, and E. coli, where they exhibit considerable inhibitory activity. The most potent compound among the tested series, compound 7c showed bactericidal activity in the time-kill curve against E. coli. Compound 7c also showed inhibition of NF-ĸB transcriptional activity in LPS-stimulated RAW264.7 cells with IC50 of 19.23 μM. The effect of compound 7c was also investigated in experimentally induced periodontitis in rats on various indices of oxidative stress (MDA, SOD, and GSH), inflammation (TNF-α, IL-1β, and IL-6), and apoptosis. It has been found that compound 7c significantly inhibits oxidative stress, inflammation, and apoptosis in a dose-dependent manner. Compound 7c also inhibits the expression of COX-2 and iNOS as shown by western blot analysis.Entities:
Keywords: COX-2; RAW264.7 cells; hybrid compounds; synthesis
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Year: 2021 PMID: 34227156 DOI: 10.1002/ddr.21851
Source DB: PubMed Journal: Drug Dev Res ISSN: 0272-4391 Impact factor: 4.360