Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/114809
DC FieldValueLanguage
dc.contributor.authorSilva, Jorge Miguel Alves-
dc.contributor.authorGonçalves, Maria José-
dc.contributor.authorSilva, Ana-
dc.contributor.authorCavaleiro, Carlos-
dc.contributor.authorCruz, M. Teresa-
dc.contributor.authorSalgueiro, Lígia-
dc.date.accessioned2024-04-12T10:35:57Z-
dc.date.available2024-04-12T10:35:57Z-
dc.date.issued2023-01-15-
dc.identifier.issn2079-6382pt
dc.identifier.urihttps://hdl.handle.net/10316/114809-
dc.description.abstractFungal infections and the accompanying inflammatory responses are associated with great morbidity and mortality due to the frequent relapses triggered by an increased resistance to antifungal agents. Furthermore, this inflammatory state can be exacerbated during inflammaging and cellular senescence. Essential oils (EO) are receiving increasing interest in the field of drug discovery due to their lipophilic nature and complex composition, making them suitable candidates in the development of new antifungal drugs and modulators of numerous molecular targets. This work chemically characterized the EO from Santolina rosmarinifolia L., collected in Setúbal (Portugal), and assessed its antifungal potential by determining its minimum inhibitory (MIC) and minimum lethal (MLC) concentration in accordance with the Clinical Laboratory Standard Guidelines (CLSI) guidelines, as well as its effect on several Candida albicans virulence factors. The anti-inflammatory effect was unveiled using lipopolysaccharide (LPS)-stimulated macrophages by assessing several pro-inflammatory mediators. The wound healing and anti-senescence potential of the EO was also disclosed. The EO was mainly characterized by β-pinene (29.6%), borneol (16.9%), myrcene (15.4%) and limonene (5.7%). It showed a strong antifungal effect against yeasts and filamentous fungi (MIC = 0.07-0.29 mg/mL). Furthermore, it inhibited dimorphic transition (MIC/16), decreased biofilm formation with a preeminent effect after 24 h (MIC/2) and disrupted preformed biofilms in C. albicans. Additionally, the EO decreased nitric oxide (NO) release (IC50 = 0.52 mg/mL) and pro-IL-1β and inducible nitric oxide synthase (iNOS) expression in LPS-stimulated macrophages, promoted wound healing (91% vs. 81% closed wound) and reduced cellular senescence (53% vs. 73% β-galactosidase-positive cells). Overall, this study highlights the relevant pharmacological properties of S. rosmarinifolia, opening new avenues for its industrial exploitation.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationUIDB/04539/2020pt
dc.relationUIDP/04539/2020pt
dc.relationLA/P/0058/2020pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectanti-inflammatorypt
dc.subjectantifungalpt
dc.subjectAsteraceaept
dc.subjectdimorphic transitionpt
dc.subjectbiofilmpt
dc.subjectsenescencept
dc.subjectwound healingpt
dc.titleChemical Profile, Anti-Microbial and Anti-Inflammaging Activities of Santolina rosmarinifolia L. Essential Oil from Portugalpt
dc.typearticle-
degois.publication.firstPage179pt
degois.publication.issue1pt
degois.publication.titleAntibioticspt
dc.peerreviewedyespt
dc.identifier.doi10.3390/antibiotics12010179pt
degois.publication.volume12pt
dc.date.embargo2023-01-15*
uc.date.periodoEmbargo0pt
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
crisitem.author.researchunitICBR Coimbra Institute for Clinical and Biomedical Research-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCIEPQPF – Chemical Process Engineering and Forest Products Research Centre-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.parentresearchunitFaculty of Medicine-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-5270-3993-
crisitem.author.orcid0000-0002-4041-0376-
crisitem.author.orcid0000-0002-5937-1127-
crisitem.author.orcid0000-0001-9846-6754-
crisitem.author.orcid0000-0003-0948-821X-
Appears in Collections:FCTUC Eng.Química - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
FMUC Medicina - Artigos em Revistas Internacionais
I&D CIEPQPF - Artigos em Revistas Internacionais
I&D ICBR - Artigos em Revistas Internacionais
FFUC- Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons