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dc.rights.licenseopenen_US
dc.contributor.authorHALADE, Ganesh V.
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorDORBANE, Anela
dc.contributor.authorINGLE, Kevin A.
dc.contributor.authorKAIN, Vasundhara
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorSCHMITTER, Jean-Marie
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorRHOURRI-FRIH, Boutayna
dc.date.accessioned2020-04-07T09:25:42Z
dc.date.available2020-04-07T09:25:42Z
dc.date.created2017
dc.date.issued2018
dc.identifier.otherhttps://static-content.springer.com/esm/art%3A10.1007%2Fs00216-018-0863-7/MediaObjects/216_2018_863_MOESM1_ESM.pdfen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/4136
dc.description.abstractEnMyocardial infarction (MI) and subsequent progressive heart failure pathology is the major cause of death worldwide; however, the mechanism of this pathology remains unclear. The present work aimed at testing the hypothesis whether the inflammatory response is superimposed with the formation of bioactive lipid resolving molecules at the site of the injured myocardium in acute heart failure pathology post-MI. In this view, we used a robust permanent coronary ligation model to induce MI, leading to decreased contractility index with marked wall thinning and necrosis of the infarcted left ventricle. Then, we applied mass spectrometry imaging (MSI) in positive and negative ionization modes to characterize the spatial distribution of left ventricle lipids in the infarcted myocardium post-MI. After micro-extraction, liquid chromatography coupled to tandem mass spectrometry was used to confirm the structures of the imaged lipids. Statistical tools such as principal component analysis were used to establish a comprehensive visualization of lipid profile changes in MI and no-MI hearts. Resolving bioactive molecules such as resolvin (Rv) D1, RvD5, RvE3, 17-HDHA, LXA4, and 18-HEPE were detected in negative ion mode MSI, whereas phosphatidyl cholines (PC) and oxidized derivatives thereof were detected in positive ion mode. MSI-based analysis demonstrated a significant increase in resolvin bioactive lipids with comprehensive lipid remodeling at the site of infarction. These results clearly indicate that infarcted myocardium is the primary location of inflammation-resolution pathomechanics which is critical for resolution of inflammation and heart failure pathophysiology. Graphical abstract Applied scheme to determine comprehensive lipidomics in failing and non-failing heart.
dc.language.isoENen_US
dc.subject.enMyocardial infarction
dc.subject.enLipids
dc.subject.enIschemic myocardium
dc.subject.enResolution of inflammation
dc.subject.enBioactive lipid molecules
dc.title.enComprehensive targeted and non-targeted lipidomics analyses in failing and non-failing heart
dc.title.alternativeAnal Bioanal Chemen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s00216-018-0863-7en_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalAnalytical and Bioanalytical Chemistryen_US
bordeaux.page1965-1976en_US
bordeaux.volume410en_US
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248
bordeaux.issue7en_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-02534761
hal.version1
hal.date.transferred2020-04-07T09:25:47Z
hal.exporttrue
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