Effects of activation of μ-, κ1-, δ1-, δ2-, and ORL1-receptors on heart resistance to the pathogenic action of delayed ischemia and reperfusion-Reference-Cited by-同舟云学术

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Effects of activation of μ-, κ1-, δ1-, δ2-, and ORL1-receptors on heart resistance to the pathogenic action of delayed ischemia and reperfusion

Published:2009-07-10 Issue:4 Volume:36 Page:354-362
ISSN:1062-3590
Container-title:Biology Bulletin
language:en
Short-container-title:Biol Bull Russ Acad Sci

Author:

Lishmanov Yu. B.,Maslov L. N.,Barzakh E. I.,Krylatov A. V.,Oltgen P. R.,Browne S. A.,Govindashvami M.

Publisher

Pleiades Publishing Ltd

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

Link

http://link.springer.com/content/pdf/10.1134/S1062359009040062.pdf

Reference58 articles.

1. Aitchison, K.A., Baxter, G.F., Awan, M.M., et al., Opposing Effects on Infarction of Delta and Kappa Opioid Receptor Activation in the Isolated Rat Heart: Implications for Ischemic Preconditioning, Basic Res. Cardiol., 2000, vol. 95, no. 1, pp. 1–10.

2. Birch, P.J., Rogers, H., Hayes, A.G., et al., Neuroprotective Actions of GR89696, a Highly Potent and Selective-Opioid Receptor Agonist, Br. J. Pharmacol., 1991, vol. 103, pp. 1819–1823.

3. Cadet, P., Bilfinger, T.V., Fimiani, C., et al., Human Vascular and Cardiac Endothelia Express Mu Opiate Receptor Transcripts, Endothelium, 2000, vol. 7, pp. 185–191.

4. Cao, Z., Liu, L., and Van Winkle, D.M., Activation of δ- and κ-Opioid Receptors by Opioid Peptides Protects Cardiomyocytes via KATP Channels, Am. J. Physiol. Heart Circ. Physiol., 2003, vol. 285, no. 3, pp. H1032–H1039.

5. Chen, M., Zhou, J.J., Kam, K.W., et al., Roles of KATP Channels in Delayed Cardioprotection and Intracellular Ca2+ in the Rat Heart As Revealed by κ-Opioid Receptor Stimulation with U50488H, Br. J. Pharmacol., 2003, vol. 140, no. 4, pp. 750–758.

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1. Ischemia, reperfusion and preconditioning: traditional and new approaches for treatment of myocardial infarction;Reviews on Clinical Pharmacology and Drug Therapy;2016-09-15

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