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Release of Mitochondrial and Nuclear DNA During On-Pump Heart Surgery: Kinetics and Relation to Extracellular Vesicles.
Baysa, Anton; Fedorov, Anton; Kondratov, Kirill; Ruusalepp, Arno; Minasian, Sarkis; Galagudza, Michael; Popov, Maxim; Kurapeev, Dmitry; Yakovlev, Alexey; Valen, Guro; Kostareva, Anna; Vaage, Jarle; Stensløkken, Kåre-Olav.
Affiliation
  • Baysa A; Division of Physiology, Department of Molecular Medicine, Institute of Basic Medical Science, University of Oslo, Postbox 1103, Blindern, 0317, Oslo, Norway.
  • Fedorov A; Center for Heart Failure Research, University of Oslo, Oslo, Norway.
  • Kondratov K; Almazov National Medical Research Centre, Saint Petersburg, Russia.
  • Ruusalepp A; Department of Cytology and Histology, Saint Petersburg State University, Saint Petersburg, Russia.
  • Minasian S; Almazov National Medical Research Centre, Saint Petersburg, Russia.
  • Galagudza M; Department of Cardiac Surgery, Tartu University Hospital, Tartu, Estonia.
  • Popov M; Almazov National Medical Research Centre, Saint Petersburg, Russia.
  • Kurapeev D; Almazov National Medical Research Centre, Saint Petersburg, Russia.
  • Yakovlev A; Almazov National Medical Research Centre, Saint Petersburg, Russia.
  • Valen G; Almazov National Medical Research Centre, Saint Petersburg, Russia.
  • Kostareva A; Almazov National Medical Research Centre, Saint Petersburg, Russia.
  • Vaage J; Division of Physiology, Department of Molecular Medicine, Institute of Basic Medical Science, University of Oslo, Postbox 1103, Blindern, 0317, Oslo, Norway.
  • Stensløkken KO; Center for Heart Failure Research, University of Oslo, Oslo, Norway.
J Cardiovasc Transl Res ; 12(3): 184-192, 2019 06.
Article in En | MEDLINE | ID: mdl-30542983
During heart surgery with cardiopulmonary bypass (CPB), the release of mitochondrial (mtDNA) and nuclear DNA (nDNA) and their association to extracellular vesicles were investigated. In patients undergoing elective coronary artery bypass grafting (CABG, n = 12), blood was sampled before, during, and after surgery from peripheral artery, pulmonary artery, and the coronary sinus. Plasma was separated in three fractions: microvesicles, exosomes, and supernatant. mtDNA and nDNA were measured by qPCR. mtDNA and nDNA levels increased after start of surgery, but before CPB, and increased further during CPB. mtDNA copy number was about 1000-fold higher than nDNA. mtDNA was predominantly localized to the vesicular fractions in plasma, whereas nDNA was predominantly in the supernatant. The amount of free mtDNA increased after surgery. There was no net release or disappearance of DNAs across the pulmonary, systemic, or coronary circulation. Extracellular DNAs, in particular mtDNA, may be important contributors to the whole-body inflammation during CPB.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Cardiopulmonary Bypass / Coronary Artery Bypass / Exosomes / Cell-Free Nucleic Acids Limits: Humans Language: En Journal: J Cardiovasc Transl Res Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2019 Document type: Article Affiliation country: Norway Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Cardiopulmonary Bypass / Coronary Artery Bypass / Exosomes / Cell-Free Nucleic Acids Limits: Humans Language: En Journal: J Cardiovasc Transl Res Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2019 Document type: Article Affiliation country: Norway Country of publication: United States