Development and translation of thiometallate sulfide donors using a porcine model of coronary occlusion and reperfusion.

Gasotransmitter Ischaemia Mitochondria Reactive oxygen species Reperfusion injury Selenoprotein Tetrathiomolybdate

Journal

Redox biology
ISSN: 2213-2317
Titre abrégé: Redox Biol
Pays: Netherlands
ID NLM: 101605639

Informations de publication

Date de publication:
25 Apr 2024
Historique:
received: 15 02 2024
revised: 12 04 2024
accepted: 22 04 2024
medline: 1 5 2024
pubmed: 1 5 2024
entrez: 30 4 2024
Statut: aheadofprint

Résumé

Sulfide-releasing compounds reduce reperfusion injury by decreasing mitochondria-derived reactive oxygen species production. We previously characterised ammonium tetrathiomolybdate (ATTM), a clinically used copper chelator, as a sulfide donor in rodents. Here we assessed translation to large mammals prior to clinical testing. In healthy pigs an intravenous ATTM dose escalation revealed a reproducible pharmacokinetic/pharmacodynamic (PK/PD) relationship with minimal adverse clinical or biochemical events. In a myocardial infarction (1-h occlusion of the left anterior descending coronary artery)-reperfusion model, intravenous ATTM or saline was commenced just prior to reperfusion. ATTM protected the heart (24-h histological examination) in a drug-exposure-dependent manner (r

Identifiants

pubmed: 38688060
pii: S2213-2317(24)00143-5
doi: 10.1016/j.redox.2024.103167
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103167

Informations de copyright

Crown Copyright © 2024. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: AD and MS are developing thiometallates for the treatment of reperfusion injury. JM, MS and AD hold patents on therapeutic uses of ammonium tetrathiomolybdate.

Auteurs

Thomas W Johnson (TW)

Translational Biomedical Research Centre (TBRC), Faculty of Health Science, University of Bristol, UK.

James Holt (J)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK.

Anna Kleyman (A)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK.

Shengyu Zhou (S)

Institute of Pharmaceutical Science, King's College London, London, UK; Centre for Pharmaceutical Medicine Research, King's College London, London, UK.

Eva Sammut (E)

Translational Biomedical Research Centre (TBRC), Faculty of Health Science, University of Bristol, UK.

Vito Domenico Bruno (VD)

Translational Biomedical Research Centre (TBRC), Faculty of Health Science, University of Bristol, UK.

Charlotte Gaupp (C)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK.

Giacomo Stanzani (G)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK.

John Martin (J)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK.

Pietro Arina (P)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK.

Julia Deutsch (J)

Translational Biomedical Research Centre (TBRC), Faculty of Health Science, University of Bristol, UK.

Raimondo Ascione (R)

Translational Biomedical Research Centre (TBRC), Faculty of Health Science, University of Bristol, UK.

Mervyn Singer (M)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK. Electronic address: m.singer@ucl.ac.uk.

Alex Dyson (A)

Bloomsbury Institute of Intensive Care Medicine, Division of Medicine, University College London, London, UK; Institute of Pharmaceutical Science, King's College London, London, UK; Centre for Pharmaceutical Medicine Research, King's College London, London, UK. Electronic address: alex.dyson@kcl.ac.uk.

Classifications MeSH