Effect of maturation on the resistance of rat hearts against ischemia. Study of potential molecular mechanisms
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
26674286
DOI
10.33549/physiolres.933222
PII: 933222
Knihovny.cz E-zdroje
- MeSH
- časové faktory MeSH
- fosforylace MeSH
- funkce levé komory srdeční MeSH
- fyziologická adaptace MeSH
- infarkt myokardu metabolismus patologie patofyziologie prevence a kontrola MeSH
- ischemické přivykání metody MeSH
- komorový tlak (srdce) MeSH
- koronární cirkulace MeSH
- modely nemocí na zvířatech MeSH
- myokard metabolismus patologie MeSH
- obnova funkce MeSH
- potkani Wistar MeSH
- preparace izolovaného srdce MeSH
- proteinkinasa C-epsilon metabolismus MeSH
- protoonkogenní proteiny c-akt metabolismus MeSH
- reperfuzní poškození myokardu metabolismus patologie patofyziologie prevence a kontrola MeSH
- signální transdukce MeSH
- srdeční arytmie etiologie patofyziologie prevence a kontrola MeSH
- srdeční frekvence MeSH
- stárnutí metabolismus patologie MeSH
- synthasa oxidu dusnatého, typ III metabolismus MeSH
- věkové faktory MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- Nos3 protein, rat MeSH Prohlížeč
- Prkce protein, rat MeSH Prohlížeč
- proteinkinasa C-epsilon MeSH
- protoonkogenní proteiny c-akt MeSH
- synthasa oxidu dusnatého, typ III MeSH
Reduced tolerance to ischemia/reperfusion (IR) injury has been shown in elder human and animal hearts, however, the onset of this unfavorable phenotype and cellular mechanisms behind remain unknown. Moreover, aging may interfere with the mechanisms of innate cardioprotection (preconditioning, PC) and cause defects in protective cell signaling. We studied the changes in myocardial function and response to ischemia, as well as selected proteins involved in "pro-survival" pathways in the hearts from juvenile (1.5 months), younger adult (3 months) and mature adult (6 months) male Wistar rats. In Langendorff-perfused hearts exposed to 30-min ischemia/2-h reperfusion with or without prior PC (one cycle of 5-min ischemia/5-min reperfusion), we measured occurrence of reperfusion-induced arrhythmias, recovery of contractile function (left ventricular developed pressure, LVDP, in % of pre-ischemic values), and size of infarction (IS, in % of area at risk size, TTC staining and computerized planimetry). In parallel groups, LV tissue was sampled for the detection of protein levels (WB) of Akt kinase (an effector of PI3-kinase), phosphorylated (activated) Akt (p-Akt), its target endothelial NO synthase (eNOS) and protein kinase Cepsilon (PKCepsilon) as components of "pro-survival" cascades. Maturation did not affect heart function, however, it impaired cardiac response to lethal IR injury (increased IS) and promoted arrhythmogenesis. PC reduced the occurrence of malignant arrhythmias, IS and improved LVDP recovery in the younger animals, while its efficacy was attenuated in the mature adults. Loss of PC protection was associated with age-dependent reduced Akt phosphorylation and levels of eNOS and PKCepsilon in the hearts of mature animals compared with the younger ones, as well as with a failure of PC to upregulate these proteins. Aging-related alterations in myocardial response to ischemia may be caused by dysfunction of proteins involved in protective cell signaling that may occur already during the process of maturation.
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