Selective replacement of mitochondrial DNA increases the cardioprotective effect of chronic continuous hypoxia in spontaneously hypertensive rats
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
28292971
DOI
10.1042/cs20170083
PII: CS20170083
Knihovny.cz E-resources
- Keywords
- chronic hypoxia, heart, hypertension, ischaemia–reperfusion injury, mitochondrial genome, mitochondrial permeability transition pore,
- MeSH
- Chronic Disease MeSH
- Genome, Mitochondrial genetics MeSH
- Hypoxia * MeSH
- Myocardial Infarction genetics metabolism pathology MeSH
- Rats MeSH
- DNA, Mitochondrial genetics MeSH
- Mitochondrial Proteins genetics metabolism MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Rats, Inbred BN MeSH
- Rats, Inbred SHR MeSH
- Rats, Transgenic MeSH
- Mitochondrial Permeability Transition Pore MeSH
- Myocardial Reperfusion Injury genetics metabolism physiopathology MeSH
- Electron Transport Complex IV genetics metabolism MeSH
- Mitochondria, Heart genetics metabolism MeSH
- Mitochondrial Membrane Transport Proteins metabolism MeSH
- Blotting, Western MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- DNA, Mitochondrial MeSH
- Mitochondrial Proteins MeSH
- Mitochondrial Permeability Transition Pore MeSH
- Electron Transport Complex IV MeSH
- Mitochondrial Membrane Transport Proteins MeSH
Mitochondria play an essential role in improved cardiac ischaemic tolerance conferred by adaptation to chronic hypoxia. In the present study, we analysed the effects of continuous normobaric hypoxia (CNH) on mitochondrial functions, including the sensitivity of the mitochondrial permeability transition pore (MPTP) to opening, and infarct size (IS) in hearts of spontaneously hypertensive rats (SHR) and the conplastic SHR-mtBN strain, characterized by the selective replacement of the mitochondrial genome of SHR with that of the more ischaemia-resistant brown Norway (BN) strain. Rats were adapted to CNH (10% O2, 3 weeks) or kept at room air as normoxic controls. In the left ventricular mitochondria, respiration and cytochrome c oxidase (COX) activity were measured using an Oxygraph-2k and the sensitivity of MPTP opening was assessed spectrophotometrically as Ca2+-induced swelling. Myocardial infarction was analysed in anaesthetized open-chest rats subjected to 20 min of coronary artery occlusion and 3 h of reperfusion. The IS reached 68±3.0% and 65±5% of the area at risk in normoxic SHR and SHR-mtBN strains, respectively. CNH significantly decreased myocardial infarction to 46±3% in SHR. In hypoxic SHR-mtBN strain, IS reached 33±2% and was significantly smaller compared with hypoxic SHR. Mitochondria isolated from hypoxic hearts of both strains had increased detergent-stimulated COX activity and were less sensitive to MPTP opening. The maximum swelling rate was significantly lower in hypoxic SHR-mtBN strain compared with hypoxic SHR, and positively correlated with myocardial infarction in all experimental groups. In conclusion, the mitochondrial genome of SHR modulates the IS-limiting effect of adaptation to CNH by affecting mitochondrial energetics and MPTP sensitivity to opening.
Deparment of Physiology Faculty of Science Charles University Viničná 7 Prague 12800 Czech Republic
Institute of Physiology Czech Academy of Sciences Vídeňská 1083 Prague 14220 Czech Republic
References provided by Crossref.org
Sixty Years of Heart Research in the Institute of Physiology of the Czech Academy of Sciences
Desmin Knock-Out Cardiomyopathy: A Heart on the Verge of Metabolic Crisis