Abstract
Pretreatment with isoflurane decreased myocardial infarction size in young rats (3-5 months) but not in old rats (20-24 months). To understand the mechanisms underlying the failure to protect the old myocardium, differences in phosphorylation of Akt/GSK-3β and age-associated differences in mitochondrial permeability transition pore (mPTP) opening in the aging heart in vivo were measured. Isoflurane significantly increased Akt and GSK-3β phosphorylation in the young groups. In contrast, levels of p-Akt and p-GSK-3β were highly elevated in the old sham control groups. Isoflurane preconditioning significantly reduced the fall in NAD+ levels induced by ischemia/reperfusion injury in the young animals, reflecting the inhibition of mPTP opening. In the old animals, however, isoflurane failed to prevent the fall in NAD+ levels induced by ischemia/reperfusion injury. Lack of isoflurane-induced cardioprotective effects, seen in the old animals, can be explained by age-related differences in Akt/GSK-3β signaling pathway and the inability to reduce mPTP opening following ischemia/reperfusion injury. © The Author 2010.
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Zhu, J., Rebecchi, M. J., Tan, M., Glass, P. S. A., Brink, P. R., & Liu, L. (2010). Age-associated differences in activation of akt/GSK-3β signaling pathways and inhibition of mitochondrial permeability transition pore opening in the rat heart. Journals of Gerontology - Series A Biological Sciences and Medical Sciences, 65 A(6), 611–619. https://doi.org/10.1093/gerona/glq035
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