Protective role of new nitrogen compounds on ROS/RNS-mediated damage to PC12 cells

dc.contributor.authorSilva, João P.
dc.contributor.authorProença, M. Fernanda R. P.
dc.contributor.authorCoutinho, O. P.
dc.date.accessioned2008-03-10T21:01:31Z
dc.date.available2008-03-10T21:01:31Z
dc.date.issued2008
dc.description.abstractReactive oxygen (ROS) and nitrogen (RNS) species are known to be involved in many degenerative diseases. This study reports four new nitrogen compounds from organic synthesis, identified as FMA4, FMA7, FMA762 and FMA796, which differ mainly by the number of hydroxyl groups within their phenolic unit. Their potential role as antioxidants was evaluated in PC12 cells by assessing their protection against oxidative and nitrosative insults. The four compounds, and particularly FMA762 and FMA796, were able to protect cells against lipid peroxidation and intracellular ROS/RNS formation to a great extent. Their protective effects were likely mediated by their free radicals scavenging ability, as they appeared to be involved neither in the induction of natural antioxidant enzymes like GSH-PX and SOD, nor in the inhibition of NOS. Nevertheless, these results suggest a promising potential for these compounds as ROS/RNS scavengers in pathologies where oxidative/ nitrosative stress are involved.eng
dc.description.sponsorshipFundação para a Ciência e Tecnologia (FCT)por
dc.distributioninternationaleng
dc.identifier.citation"Free Radical Research". ISSN 1071-5762. 42:1 (2008) 57-69.eng
dc.identifier.doi10.1080/10715760701787719por
dc.identifier.issn1071-5762eng
dc.identifier.pmid18324524por
dc.identifier.urihttps://hdl.handle.net/1822/7707
dc.language.isoengeng
dc.peerreviewedyeseng
dc.publisherInforma Healthcareeng
dc.rightsopenAccesseng
dc.subjectlipid peroxidationpor
dc.subjectoxidative stresspor
dc.subjectnitrogen compoundspor
dc.subjectantioxidantspor
dc.subjectnitrosative stresspor
dc.subject.wosScience & Technologypor
dc.titleProtective role of new nitrogen compounds on ROS/RNS-mediated damage to PC12 cellseng
dc.typearticlepor
dspace.entity.typePublicationen
oaire.citationEndPage69por
oaire.citationIssue1por
oaire.citationStartPage57por
oaire.citationVolume42por
sdum.journalFree Radical Researchpor
sdum.number1eng
sdum.pagination57-69eng
sdum.publicationstatuspublishedeng
sdum.volume42eng

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