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dc.rights.licenseopenen_US
dc.contributor.authorPRAG, Hiran A
dc.contributor.authorAKSENTIJEVIC, Dunja
dc.contributor.authorDANNHORN, Andreas
dc.contributor.authorGILES, Abigail V
dc.contributor.authorMULVEY, John F
dc.contributor.authorSAUCHANKA, Olga
dc.contributor.authorDU, Luping
dc.contributor.authorBATES, Georgina
dc.contributor.authorREINHOLD, Johannes
dc.contributor.authorKULA-ALWAR, Duvaraka
dc.contributor.authorXU, Zhelong
hal.structure.identifierCentre de résonance magnétique des systèmes biologiques [CRMSB]
dc.contributor.authorPELLERIN, Luc
dc.contributor.authorGOODWIN, Richard J A
dc.contributor.authorMURPHY, Michael P
dc.contributor.authorKRIEG, Thomas
dc.date.accessioned2022-11-22T08:41:43Z
dc.date.available2022-11-22T08:41:43Z
dc.date.issued2022-09-02
dc.identifier.issn1524-4571en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170338
dc.description.abstractEnInhibiting SDH (succinate dehydrogenase), with the competitive inhibitor malonate, has shown promise in ameliorating ischemia/reperfusion injury. However, key for translation to the clinic is understanding the mechanism of malonate entry into cells to enable inhibition of SDH, its mitochondrial target, as malonate itself poorly permeates cellular membranes. The possibility of malonate selectively entering the at-risk heart tissue on reperfusion, however, remains unexplored. C57BL/6J mice, C2C12 and H9c2 myoblasts, and HeLa cells were used to elucidate the mechanism of selective malonate uptake into the ischemic heart upon reperfusion. Cells were treated with malonate while varying pH or together with transport inhibitors. Mouse hearts were either perfused ex vivo (Langendorff) or subjected to in vivo left anterior descending coronary artery ligation as models of ischemia/reperfusion injury. Succinate and malonate levels were assessed by liquid chromatography-tandem mass spectrometry LC-MS/MS, in vivo by mass spectrometry imaging, and infarct size by TTC (2,3,5-triphenyl-2H-tetrazolium chloride) staining. Malonate was robustly protective against cardiac ischemia/reperfusion injury, but only if administered at reperfusion and not when infused before ischemia. The extent of malonate uptake into the heart was proportional to the duration of ischemia. Malonate entry into cardiomyocytes in vivo and in vitro was dramatically increased at the low pH (≈6.5) associated with ischemia. This increased uptake of malonate was blocked by selective inhibition of MCT1 (monocarboxylate transporter 1). Reperfusion of the ischemic heart region with malonate led to selective SDH inhibition in the at-risk region. Acid-formulation greatly enhances the cardioprotective potency of malonate. Cardioprotection by malonate is dependent on its entry into cardiomyocytes. This is facilitated by the local decrease in pH that occurs during ischemia, leading to its selective uptake upon reperfusion into the at-risk tissue, via MCT1. Thus, malonate's preferential uptake in reperfused tissue means it is an at-risk tissue-selective drug that protects against cardiac ischemia/reperfusion injury.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAnimals
dc.subject.enChromatography
dc.subject.enLiquid
dc.subject.enHeLa Cells
dc.subject.enHumans
dc.subject.enIschemia
dc.subject.enMalonates
dc.subject.enMice
dc.subject.enMice
dc.subject.enInbred C57BL
dc.subject.enMyocardial Reperfusion Injury
dc.subject.enMyocytes
dc.subject.enCardiac
dc.subject.enTandem Mass Spectrometry
dc.title.enIschemia-Selective Cardioprotection by Malonate for Ischemia/Reperfusion Injury.
dc.title.alternativeCirc Resen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1161/CIRCRESAHA.121.320717en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed35959683en_US
bordeaux.journalCirculation Researchen_US
bordeaux.page528-541en_US
bordeaux.volume131en_US
bordeaux.hal.laboratoriesCentre de Résonance Magnétique des Systèmes Biologiques (CRMSB) - UMR 5536en_US
bordeaux.issue6en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03864945
hal.version1
hal.date.transferred2022-11-22T08:42:14Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Circulation%20Research&rft.date=2022-09-02&rft.volume=131&rft.issue=6&rft.spage=528-541&rft.epage=528-541&rft.eissn=1524-4571&rft.issn=1524-4571&rft.au=PRAG,%20Hiran%20A&AKSENTIJEVIC,%20Dunja&DANNHORN,%20Andreas&GILES,%20Abigail%20V&MULVEY,%20John%20F&rft.genre=article


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