Abstract |
We studied the effects of μ- opioid receptor activation in vivo and in vitro on the tolerance of isolated perfused rat heart to global ischemia (45 min) and reperfusion (30 min). Stimulation of μ-receptors in vivo by intraperitoneal administration of μ- opioid receptor agonist DAMGO (0.1 mg/kg) reduced reperfusion release of creatinine phosphokinase and promoted aggravation of postischemic systolic and diastolic dysfunction of the isolated heart. Activation of μ- opioid receptors in vitro by addition of selective agonist DAMGO in a concentration of 170 nM to perfusion solution had no effect on necrotic death of cardiomyocytes and aggravated reperfusion stunning of the heart.
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Authors | T V Lasukova, L N Maslov, A S Gorbunov |
Journal | Bulletin of experimental biology and medicine
(Bull Exp Biol Med)
Vol. 159
Issue 6
Pg. 722-5
(Oct 2015)
ISSN: 1573-8221 [Electronic] United States |
PMID | 26519265
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Receptors, Opioid, mu
- Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
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Topics |
- Animals
- Cell Death
(drug effects)
- Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
(pharmacology, therapeutic use)
- Heart
(drug effects, physiology)
- Male
- Myocardial Contraction
(drug effects)
- Myocardial Ischemia
(pathology, physiopathology)
- Myocardial Reperfusion Injury
(pathology, physiopathology)
- Myocardium
(pathology)
- Myocytes, Cardiac
(drug effects, pathology)
- Necrosis
- Organ Culture Techniques
- Rats
- Rats, Wistar
- Receptors, Opioid, mu
(agonists)
- Reperfusion
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