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New Drug Targets and Preclinical Modelling Recommendations for Treating Acute Myocardial Infarction.
Cao, Yuanzhao; Redd, Meredith A; Fang, Chen; Mizikovsky, Dalia; Li, Xichun; Macdonald, Peter S; King, Glenn F; Palpant, Nathan J.
Afiliação
  • Cao Y; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia.
  • Redd MA; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia.
  • Fang C; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia.
  • Mizikovsky D; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia.
  • Li X; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia.
  • Macdonald PS; Cardiopulmonary Transplant Unit, St Vincent's Hospital, Sydney, NSW, Australia.
  • King GF; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia; Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science, The University of Queensland, Brisbane, Qld, Australia.
  • Palpant NJ; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Qld, Australia. Electronic address: n.palpant@uq.edu.au.
Heart Lung Circ ; 32(7): 852-869, 2023 Jul.
Article em En | MEDLINE | ID: mdl-37230806
Acute myocardial infarction (AMI) is the leading cause of morbidity and mortality worldwide and the primary underlying risk factor for heart failure. Despite decades of research and clinical trials, there are no drugs currently available to prevent organ damage from acute ischaemic injuries of the heart. In order to address the increasing global burden of heart failure, drug, gene, and cell-based regeneration technologies are advancing into clinical testing. In this review we highlight the burden of disease associated with AMI and the therapeutic landscape based on market analyses. New studies revealing the role of acid-sensitive cardiac ion channels and other proton-gated ion channels in cardiac ischaemia are providing renewed interest in pre- and post-conditioning agents with novel mechanisms of action that may also have implications for gene- and cell-based therapeutics. Furthermore, we present guidelines that couple new cell technologies and data resources with traditional animal modelling pipelines to help de-risk drug candidates aimed at treating AMI. We propose that improved preclinical pipelines and increased investment in drug target identification for AMI is critical to stem the increasing global health burden of heart failure.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão Miocárdica / Insuficiência Cardíaca / Infarto do Miocárdio Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão Miocárdica / Insuficiência Cardíaca / Infarto do Miocárdio Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article