Literature DB >> 16597498

Proteasomal proteolysis in anoxia-reoxygenation, preconditioning and postconditioning of isolated cardiomyocytes.

Victor E Dosenko1, Vasyl S Nagibin, Lesya V Tumanovskaya, Vyacheslav Yu Zagoriy, Alexey A Moibenko, Jarle Vaage.   

Abstract

The role of proteasomal proteolysis in the pathogenesis of ischemia-reperfusion is being actively studied. To evaluate the participation of the proteasome in the preconditioning and postconditioning phenomena we used primary culture of neonatal cardiomyocytes. This culture was undergone 30min of anoxia followed by 60min of reoxygenation. Preconditioning was modeled by three cycles of 3min anoxia followed by 3min reoxygenation. Postconditioning was modeled by three cycles of 1min reoxygenation followed by 1min anoxia, respectively. Clasto-lactacystin beta-lactone, a specific proteasome inhibitor, was added to the culture medium right before the cycles of preconditioning or postconditioning in the dose that does not cause cell death (2.5muM). Percentages of living, necrotic, and apoptotic cells were determined by staining with bisbenzimide and propidium iodide. Autophagy was demonstrated by staining vacuolar structures with monodansyl cadaverine. Proteasomal activity was determined by cleavage intensity of specific fluorogenic substrates. Trypsin-like, chymotrypsin-like and peptidyl-glutamyl peptide-hydrolyzing (PGPH) activities were decreased after anoxia. Reoxygenation has led to the increase in trypsin-like and chymotrypsin-like activities comparing to anoxia, but these parameters have never reached the control levels. PGPH activity has been restored up to the initial level. Preconditioning and postconditioning increased numbers of living cells and decreased that of necrotic, apoptotic and autophagic cells. Paradoxically, it was established that proteasome inhibitors prevented the necrotic and apoptotic cell death of cardiomyocytes in anoxia-reoxygenation, but in the same concentration abolished the effects of preconditioning and postconditioning. Low doses of proteasome inhibitors, particularly the ones used in our experiments, resulted in the abolishing of preconditioning and postconditioning phenomena, but at the same time led to the increase of the population of living cells in anoxia-reoxygenation, and can be considered as potential pharmacological agents of preconditioning and postconditioning.

Entities:  

Year:  2006        PMID: 16597498     DOI: 10.1016/j.pathophys.2006.01.003

Source DB:  PubMed          Journal:  Pathophysiology        ISSN: 0928-4680


  7 in total

1.  Effect of a low dose of proteasome inhibitor on cell death and gene expression in neonatal rat cardiomyocyte cultures exposed to anoxia-reoxygenation.

Authors:  Olga V Surova; Vasyl S Nagibin; Lesya V Tumanovskaya; Victor E Dosenko; Alexey A Moibenko
Journal:  Exp Clin Cardiol       Date:  2009

2.  Does proteasome regulate the level of microRNA-1 in cardiomyocytes? Application to anoxia-reoxygenation.

Authors:  Veronika Gurianova; Dmytro Stroy; Peter Kruzliak; Victoria Kyrichenko; Alex Moibenko; Victor Dosenko
Journal:  Mol Cell Biochem       Date:  2015-02-28       Impact factor: 3.396

Review 3.  Protective and deleterious effects of autophagy in the setting of myocardial ischemia/reperfusion injury: an overview.

Authors:  Behnaz Mokhtari; Reza Badalzadeh
Journal:  Mol Biol Rep       Date:  2022-09-15       Impact factor: 2.742

Review 4.  Protective ischaemia in patients: preconditioning and postconditioning.

Authors:  Asger Granfeldt; David J Lefer; Jakob Vinten-Johansen
Journal:  Cardiovasc Res       Date:  2009-04-27       Impact factor: 10.787

Review 5.  Cardioprotection requires taking out the trash.

Authors:  Roberta A Gottlieb; Kim D Finley; Robert M Mentzer
Journal:  Basic Res Cardiol       Date:  2009-02-26       Impact factor: 17.165

Review 6.  Reperfusion injury salvage kinase signalling: taking a RISK for cardioprotection.

Authors:  Derek J Hausenloy; Derek M Yellon
Journal:  Heart Fail Rev       Date:  2007-12       Impact factor: 4.214

7.  Inhibition of autophagy contributes to ischemic postconditioning-induced neuroprotection against focal cerebral ischemia in rats.

Authors:  Li Gao; Teng Jiang; Jun Guo; Yi Liu; Guiyun Cui; Lize Gu; Lingying Su; Yingdong Zhang
Journal:  PLoS One       Date:  2012-09-28       Impact factor: 3.240

  7 in total

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