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Naunyn Schmiedebergs Arch Pharmacol. 2020 Apr;393(4):629-638. doi: 10.1007/s00210-019-01761-9. Epub 2019 Nov 27.

Isoespintanol, a monoterpene isolated from oxandra cf xylopioides, ameliorates the myocardial ischemia-reperfusion injury by AKT/PKCε/eNOS-dependent pathways.

Author information

1
Centro de Investigaciones Cardiovasculares ¨Dr Horacio E. Cingolani¨, CCT-CONICET, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, 60 y 120, 1900, La Plata, Argentina.
2
Laboratorio de Ciencias de los Alimentos, Facultad de Ciencias, Universidad Nacional de Colombia (sede Medellín), Bogotá, Colombia.
3
Facultad de Ciencias Médicas, Universidad Nacional de La Plata CIC-PBA, La Plata, Argentina.
4
Centro de Investigaciones Cardiovasculares ¨Dr Horacio E. Cingolani¨, CCT-CONICET, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, 60 y 120, 1900, La Plata, Argentina. smosca@med.unlp.edu.ar.

Abstract

PURPOSE:

To determine the actions of isoespintanol (Isoesp) on post-ischemic myocardial and mitochondrial alterations.

METHODS:

Hearts removed from Wistar rats were perfused by 20 min. After this period, the coronary flow was interrupted by half an hour and re-established during 1 h. In the treated group, Isoesp was administered at the beginning of reperfusion. To assess the participation of ε isoform of protein kinase C (PKCε), protein kinase B (PKB/Akt), and nitric oxide synthase (NOS), hearts were treated with Isoesp plus the respective inhibitors (chelerythrine, wortmannin, and N-nitro-L-arginine methyl ester). Cell death was determined by triphenyl tetrazolium chloride staining technique. Post-ischemic recovery of contractility, oxidative stress, and content of phosphorylated forms of PKCε, Akt, and eNOS were also examined. Mitochondrial state was assessed through the measurement of calcium-mediated response, calcium retention capacity, and mitochondrial potential.

RESULTS:

Isoesp limited cell death, decreased post-ischemic dysfunction and oxidative stress, improved mitochondrial state, and increased the expression of PKCε, Akt, and eNOS phosphorylated. All these beneficial effects achieved by Isoesp were annulled by the inhibitors.

CONCLUSION:

These findings suggest that activation of Akt/eNOS and PKCε signaling pathways are involved in the development of Isoesp-induced cardiac and mitochondria tolerance to ischemia-reperfusion.

KEYWORDS:

Akt; Infarct size; Ischemia-reperfusion; Isoespintanol; PKCε; eNOS

PMID:
31776590
DOI:
10.1007/s00210-019-01761-9

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