Developmental and sex differences in cardiac tolerance to ischemia-reperfusion injury: the role of mitochondria 1
Age and sex play an essential role in the cardiac tolerance to ischemia-reperfusion injury: cardiac resistance significantly decreases during postnatal maturation and the female heart is more tolerant than the male myocardium. It is widely accepted that mitochondrial dysfunction, and particularly mi...
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Published in | Canadian journal of physiology and pharmacology Vol. 97; no. 9; pp. 808 - 814 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Canada
01.09.2019
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Subjects | |
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Abstract | Age and sex play an essential role in the cardiac tolerance to ischemia-reperfusion injury: cardiac resistance significantly decreases during postnatal maturation and the female heart is more tolerant than the male myocardium. It is widely accepted that mitochondrial dysfunction, and particularly mitochondrial permeability transition pore (MPTP) opening, plays a major role in determining the extent of cardiac ischemia-reperfusion injury. We have observed that the MPTP sensitivity to the calcium load differs in mitochondria isolated from neonatal and adult myocardium, as well as from adult male and female hearts. Neonatal and female mitochondria are more resistant both in the extent and in the rate of mitochondrial swelling induced by high calcium concentration. Our data further suggest that age- and sex-dependent specificity of the MPTP is not the result of different amounts of ATP synthase and cyclophilin D: neonatal and adult hearts, similarly as the male and female hearts, contain comparable amounts of MPTP and its regulatory protein cyclophilin D. We can speculate that the lower sensitivity of MPTP to the calcium-induced swelling may be related to the higher ischemic tolerance of both neonatal and female myocardium. |
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AbstractList | Age and sex play an essential role in the cardiac tolerance to ischemia-reperfusion injury: cardiac resistance significantly decreases during postnatal maturation and the female heart is more tolerant than the male myocardium. It is widely accepted that mitochondrial dysfunction, and particularly mitochondrial permeability transition pore (MPTP) opening, plays a major role in determining the extent of cardiac ischemia-reperfusion injury. We have observed that the MPTP sensitivity to the calcium load differs in mitochondria isolated from neonatal and adult myocardium, as well as from adult male and female hearts. Neonatal and female mitochondria are more resistant both in the extent and in the rate of mitochondrial swelling induced by high calcium concentration. Our data further suggest that age- and sex-dependent specificity of the MPTP is not the result of different amounts of ATP synthase and cyclophilin D: neonatal and adult hearts, similarly as the male and female hearts, contain comparable amounts of MPTP and its regulatory protein cyclophilin D. We can speculate that the lower sensitivity of MPTP to the calcium-induced swelling may be related to the higher ischemic tolerance of both neonatal and female myocardium. |
Author | Drahota, Z Milerova, M Ostadal, B Kolar, F Ostadalova, I Houstek, J Hlavackova, M |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30893574$$D View this record in MEDLINE/PubMed |
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Keywords | calcium-induced swelling cardiac ischemic tolerance cœur femelle ischemia–reperfusion injury neonatal heart gonflement provoqué par le calcium lésions d’ischémie–reperfusion tolérance à l’ischémie cardiaque mitochondrial permeability transition pore cœur néonatal female heart pore de transition de perméabilité mitochondriale |
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SubjectTerms | Animals Calcium - metabolism Heart - physiopathology Humans Mitochondria, Heart - metabolism Mitochondria, Heart - pathology Mitochondrial Membrane Transport Proteins - metabolism Myocardial Reperfusion Injury - metabolism Myocardial Reperfusion Injury - pathology Myocardial Reperfusion Injury - physiopathology Sex Characteristics |
Title | Developmental and sex differences in cardiac tolerance to ischemia-reperfusion injury: the role of mitochondria 1 |
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