<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Fraternale D</submitter><pubmed_abstract>In the present study, &lt;i>Monarda didyma&lt;/i> L. essential oil (isolated from the flowering aerial parts of the plant) was examined to characterize its chemotype and to evaluate, in addition to the quali-quantitative chemical analysis, the associated antioxidant and anti-inflammatory activities. The plants were grown in central Italy, Urbino (PU), Marche region. Different analyses (TLC, GC-FID, GC-MS and &lt;sup>1&lt;/sup>H-NMR) allowed the identification of twenty compounds among which carvacrol, p-cymene and thymol were the most abundant. On this basis, the chemotype examined in the present study was indicated as &lt;i>Monarda didyma&lt;/i> ct. carvacrol. The antioxidant effect was assessed by DPPH assay. Moreover, this chemotype was investigated for the anti-inflammatory effect in an &lt;i>in vitro&lt;/i> setting (&lt;i>i.e&lt;/i>., LPS-stimulated U937 cells). The decreased expression of pro-inflammatory cytokine IL-6 and the increased expression of miR-146a are suggestive of the involvement of the Toll-like receptor-4 signaling pathway. Although further studies are needed to better investigate the action mechanism/s underlying the results observed in the experimental setting, our findings show that &lt;i>M. didyma&lt;/i> essential oil is rich in bioactive compounds (mainly aromatic monoterpenes and phenolic monoterpenes) which are most likely responsible for its beneficial effect.</pubmed_abstract><journal>PeerJ</journal><pagination>e14433</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9686412</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chemical composition, antioxidant and anti-inflammatory properties of &lt;i>Monarda didyma&lt;/i> L. essential oil.</pubmed_title><pmcid>PMC9686412</pmcid><pubmed_authors>Fraternale D</pubmed_authors><pubmed_authors>Melandri D</pubmed_authors><pubmed_authors>Albertini MC</pubmed_authors><pubmed_authors>D'Adderio R</pubmed_authors><pubmed_authors>Dufat H</pubmed_authors><pubmed_authors>Bouzidi C</pubmed_authors><pubmed_authors>Di Giacomo B</pubmed_authors><pubmed_authors>Ramakrishna S</pubmed_authors><pubmed_authors>Colomba M</pubmed_authors><pubmed_authors>Coppari S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemical composition, antioxidant and anti-inflammatory properties of &lt;i>Monarda didyma&lt;/i> L. essential oil.</name><description>In the present study, &lt;i>Monarda didyma&lt;/i> L. essential oil (isolated from the flowering aerial parts of the plant) was examined to characterize its chemotype and to evaluate, in addition to the quali-quantitative chemical analysis, the associated antioxidant and anti-inflammatory activities. The plants were grown in central Italy, Urbino (PU), Marche region. Different analyses (TLC, GC-FID, GC-MS and &lt;sup>1&lt;/sup>H-NMR) allowed the identification of twenty compounds among which carvacrol, p-cymene and thymol were the most abundant. On this basis, the chemotype examined in the present study was indicated as &lt;i>Monarda didyma&lt;/i> ct. carvacrol. The antioxidant effect was assessed by DPPH assay. Moreover, this chemotype was investigated for the anti-inflammatory effect in an &lt;i>in vitro&lt;/i> setting (&lt;i>i.e&lt;/i>., LPS-stimulated U937 cells). The decreased expression of pro-inflammatory cytokine IL-6 and the increased expression of miR-146a are suggestive of the involvement of the Toll-like receptor-4 signaling pathway. Although further studies are needed to better investigate the action mechanism/s underlying the results observed in the experimental setting, our findings show that &lt;i>M. didyma&lt;/i> essential oil is rich in bioactive compounds (mainly aromatic monoterpenes and phenolic monoterpenes) which are most likely responsible for its beneficial effect.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T19:51:12.593Z</modification><creation>2025-04-04T19:51:12.593Z</creation></dates><accession>S-EPMC9686412</accession><cross_references><pubmed>36438580</pubmed><doi>10.7717/peerj.14433</doi></cross_references></HashMap>