| Literature DB >> 24316036 |
Jason N Peart1, Salvatore Pepe2, Melissa E Reichelt3, Nikkie Beckett1, Louise See Hoe1, Victoria Ozberk1, Ingrid R Niesman4, Hemal H Patel5, John P Headrick6.
Abstract
Changes in cytoprotective signaling may influence cardiac aging, and underpin sensitization to ischemic insult and desensitization to 'anti-ischemic' therapies. We tested whether age-dependent shifts in ischemia-reperfusion (I-R) tolerance in murine and human myocardium are associated with reduced efficacies and coupling of membrane, cytoplasmic and mitochondrial survival-signaling. Hormesis (exemplified in ischemic preconditioning; IPC) and expression of proteins influencing signaling/stress-resistance were also assessed in mice. Mouse hearts (18 vs. 2-4 mo) and human atrial tissue (75±2 vs. 55±2 yrs) exhibited profound age-dependent reductions in I-R tolerance. In mice aging negated cardioprotection via IPC, G-protein coupled receptor (GPCR) agonism (opioid, A1 and A3 adenosine receptors) and distal protein kinase c (PKC) activation (4 nM phorbol 12-myristate 13-acetate; PMA). In contrast, p38-mitogen activated protein kinase (p38-MAPK) activation (1 μM anisomycin), mitochondrial ATP-sensitive K(+) channel (mKATP) opening (50 μM diazoxide) and permeability transition pore (mPTP) inhibition (0.2 μM cyclosporin A) retained protective efficacies in older hearts (though failed to eliminate I-R tolerance differences). A similar pattern of change in protective efficacies was observed in human tissue. Murine hearts exhibited molecular changes consistent with altered membrane control (reduced caveolin-3, cholesterol and caveolae), kinase signaling (reduced p70 ribosomal s6 kinase; p70s6K) and stress-resistance (increased G-protein receptor kinase 2, GRK2; glycogen synthase kinase 3β, GSK3β; and cytosolic cytochrome c). In summary, myocardial I-R tolerance declines with age in association with dysfunctional hormesis and transduction of survival signals from GPCRs/PKC to mitochondrial effectors. Differential changes in proteins governing caveolar and mitochondrial function may contribute to signal dysfunction and stress-intolerance.Entities:
Keywords: AKT; Aging; CAV-3; Cardioprotection; Caveolae; Cyt c; ERK1/2; G-protein coupled receptor kinase 2; G-protein coupled receptors; GRK2; GSK3β; Hormesis; Ischemia mitochondria; MAPK/ERK kinase; MEK; PI3K; PKC; PKG; PLC; PLD; Protein kinase; RTK; Ras homolog family member A; RhoA; Stress-resistance; caveolin-3; cytochrome c; eNOS; endothelial nitric oxide synthase; extracellular signal-regulated kinase 1/2; glycogen synthase kinase 3β; mK(ATP); mPTP; mTOR; mechanistic target of rapamycin; mitochondrial ATP-gated K(+) channels; mitochondrial permeability transition pore; p38; p38-mitogen activated protein kinase; p70 ribosomal protein S6 kinase; p70s6K; phosphoinositide 3-kinase; phospholipase C; phospholipase D; protein kinase B; protein kinase G; protein kinase c; receptor tyrosine kinase
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Year: 2013 PMID： 24316036 PMCID： PMC4096533 DOI： 10.1016/j.exger.2013.11.015
Source DB: PubMed Journal: Exp Gerontol ISSN： 0531-5565 Impact factor: 4.032