Sex difference in the sensitivity of cardiac mitochondrial permeability transition pore to calcium load
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26715132
DOI
10.1007/s11010-015-2619-4
PII: 10.1007/s11010-015-2619-4
Knihovny.cz E-zdroje
- Klíčová slova
- Calcium-induced swelling, Heart, Mitochondrial permeability transition pore, Sex difference,
- MeSH
- krysa rodu Rattus MeSH
- přechodový pór mitochondriální permeability MeSH
- sexuální faktory * MeSH
- srdeční mitochondrie metabolismus MeSH
- transportní proteiny mitochondriální membrány metabolismus MeSH
- vápník metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- přechodový pór mitochondriální permeability MeSH
- transportní proteiny mitochondriální membrány MeSH
- vápník MeSH
Most of the experimental studies have revealed that female heart is more tolerant to ischemia/reperfusion (I/R) injury as compared with 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 I/R injury. The aim of the present study was, therefore, to analyze (i) whether calcium-induced swelling of cardiac mitochondria is sex-dependent and related to the degree of cardiac tolerance to I/R injury and (ii) whether changes in MPTP components-cyclophilin D (CypD) and ATP synthase-can be involved in this process. We have observed that in mitochondria isolated from rat male and female hearts the MPTP has different sensitivity to the calcium load. Female mitochondria are more resistant both in the extent and in the rate of the mitochondrial swelling at higher calcium concentration (200 µM). At low calcium concentration (50 µM) no differences were observed. Our data further suggest that sex-dependent specificity of the MPTP is not the result of different amounts of ATP synthase and CypD, or their respective ratio in mitochondria isolated from male and female hearts. Our results indicate that male and female rat hearts contain comparable content of MPTP and its regulatory protein CypD; parallel immunodetection revealed also the same contents of adenine nucleotide translocator or voltage-dependent anion channel. Increased resistance of female heart mitochondria thus cannot be explained by changes in putative components of MPTP, and rather reflects regulation of MPTP function.
Zobrazit více v PubMed
Life Sci. 2005 Apr 22;76(23):2735-49 PubMed
J Biol Chem. 2014 Jun 6;289(23):15980-5 PubMed
Physiol Res. 2009;58 Suppl 2:S1-12 PubMed
Proc Natl Acad Sci U S A. 2010 Jan 12;107(2):726-31 PubMed
Biochem Soc Trans. 2010 Aug;38(4):841-60 PubMed
J Mol Cell Cardiol. 2015 Jan;78:129-41 PubMed
Nat Cell Biol. 2007 May;9(5):550-5 PubMed
Anal Biochem. 2003 Feb 1;313(1):46-52 PubMed
Oncogene. 2015 Mar 19;34(12):1475-86 PubMed
FEBS Lett. 1978 Dec 15;96(2):373-6 PubMed
Biochim Biophys Acta. 2015 Oct;1850(10 ):2041-7 PubMed
Gen Comp Endocrinol. 2015 Jan 15;211:131-46 PubMed
Biochim Biophys Acta. 1999 Jan 6;1453(1):49-62 PubMed
Cell Calcium. 2015 Jul;58(1):18-26 PubMed
Heart Fail Rev. 2007 Dec;12(3-4):293-300 PubMed
Can J Physiol Pharmacol. 2012 Sep;90(9):1151-9 PubMed
J Cell Sci. 2010 Mar 15;123(Pt 6):894-902 PubMed
Nutr Metab Cardiovasc Dis. 2010 Jul;20(6):467-73 PubMed
J Biol Chem. 2002 Sep 20;277(38):34793-9 PubMed
Am J Physiol Heart Circ Physiol. 2011 Dec;301(6):H2191-7 PubMed
Atherosclerosis. 2009 Jun;204(2):334-41 PubMed
Anal Biochem. 1987 Nov 1;166(2):368-79 PubMed
Proc Natl Acad Sci U S A. 2013 Apr 9;110(15):5887-92 PubMed
Mt Sinai J Med. 2003 Oct;70(5):293-305 PubMed
J Biol Chem. 2009 Dec 4;284(49):33982-8 PubMed
N Engl J Med. 2008 Jul 31;359(5):473-81 PubMed
PLoS One. 2012;7(6):e38425 PubMed
Cardiovasc Res. 2007 Jun 1;74(3):456-65 PubMed
J Mol Cell Cardiol. 2015 Jan;78:100-6 PubMed
Cell Cycle. 2013 Feb 15;12(4):674-83 PubMed
Nature. 2004 Jan 29;427(6973):461-5 PubMed
Mitochondrion. 2011 Sep;11(5):722-8 PubMed
J Mol Cell Cardiol. 2015 Jan;78:35-45 PubMed
J Mol Cell Cardiol. 2004 Aug;37(2):507-13 PubMed
Proc Natl Acad Sci U S A. 2014 Jul 22;111(29):10580-5 PubMed
Aging (Albany NY). 2010 Dec;2(12):914-23 PubMed
J Mol Cell Cardiol. 2015 Jan;78:80-9 PubMed
Front Physiol. 2013 May 10;4:95 PubMed
Cardiovasc Res. 2007 Aug 1;75(3):478-86 PubMed
Physiol Bohemoslov. 1984;33(2):129-38 PubMed
Am J Physiol Heart Circ Physiol. 2006 Jun;290(6):H2644-47 PubMed
Nature. 2005 Mar 31;434(7033):658-62 PubMed
Physiol Res. 2012;61 Suppl 1:S165-72 PubMed
Anal Biochem. 1976 May 7;72:248-54 PubMed
J Biol Chem. 2011 Nov 18;286(46):40184-92 PubMed
Mol Cell Biochem. 2010 Feb;335(1-2):147-53 PubMed
Br J Pharmacol. 2014 Feb;171(3):541-54 PubMed
Arch Biochem Biophys. 2009 Nov;491(1-2):39-45 PubMed
Mol Cell Biochem. 1997 Sep;174(1-2):167-72 PubMed
J Bioenerg Biomembr. 2012 Jun;44(3):309-15 PubMed
PLoS One. 2015 Jan 23;10(1):e0117047 PubMed
J Mol Cell Cardiol. 1993 Dec;25(12):1461-9 PubMed
Arch Biochem Biophys. 1998 Jun 1;354(1):151-7 PubMed
Sex Differences in Cardiac Tolerance to Oxygen Deprivation - 40 Years of Cardiovascular Research
Sixty Years of Heart Research in the Institute of Physiology of the Czech Academy of Sciences
Short term methylphenidate treatment does not increase myocardial injury in the ischemic rat heart