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The mitochondrial permeability transition pore and cyclophilin D in cardioprotection
Authors:Fabio Di Lisa  Andrea CarpiValentina Giorgio  Paolo Bernardi
Affiliation:
  • a Department of Biomedical Sciences and CNR Institute of Neuroscience, University of Padova, 35121 Padova, Italy
  • b European Institute of Oncology, Via Adamello 16, 20139 Milan, Italy
  • Abstract:Mitochondria play a central role in heart energy metabolism and Ca2+ homeostasis and are involved in the pathogenesis of many forms of heart disease. The body of knowledge on mitochondrial pathophysiology in living cells and organs is increasing, and so is the interest in mitochondria as potential targets for cardioprotection. This critical review will focus on the permeability transition pore (PTP) and its regulation by cyclophilin (CyP) D as effectors of endogenous protective mechanisms and as potential drug targets. The complexity of the regulatory interactions underlying control of mitochondrial function in vivo is beginning to emerge, and although apparently contradictory findings still exist we believe that the network of regulatory protein interactions involving the PTP and CyPs in physiology and pathology will increase our repertoire for therapeutic interventions in heart disease. This article is part of a Special Issue entitled: Mitochondria and Cardioprotection.
    Keywords:ANT, adenine nucleotide translocase   CsA, cyclosporine A   CyP, cyclophilin   Drp1, dynamin-related protein 1   Δψm, mitochondrial membrane potential   ERK, extracellular signal regulated kinase   GSK, glycogen synthase kinase   IMM, inner mitochondrial membrane   IPC, ischemic preconditioning   IPoC, ischemic post-conditioning   mitoKATP, mitochondrial KATP channel   OMM, outer mitochondrial membrane   PKA, cyclic AMP-dependent protein kinase   PKG, cyclic GMP-dependent protein kinase   PPIase, peptidylprolyl cis-trans isomerase   PTP, permeability transition pore   ROS, reactive oxygen species   VDAC, voltage-dependent anion channel
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