Delta-opioid receptor mediates the cardioprotective effect of ischemic postconditioning / 中国应用生理学杂志
Chinese Journal of Applied Physiology
; (6): 184-189, 2008.
Article
en Zh
| WPRIM
| ID: wpr-310771
Biblioteca responsable:
WPRO
ABSTRACT
<p><b>AIM</b>To investigate the effect of 8-opioid receptors in the cardioprotection elicited by ischemic postconditioning and the underlying mechanism.</p><p><b>METHODS</b>The isolated perfused hearts of male Sprague-Dawley rats were subjected to 30 min of global ischemia followed by 120 min of reperfusion. Formazan content of myocardium was measured spectrophotometrically, and the activity of lactate dehydrogenase (LDH) in the coronary effluent was measured. In isolated ventricular myocytes hypoxic postconditioning was achieved by 3 cycles of 5 min reoxygenation/5 min hypoxia starting at the beginning of reoxygenation, and cell viability was measured.</p><p><b>RESULTS</b>In the Langendorff perfused rat heart model, ischemic postconditioning (6 cycles of 10 s reperfusion/10 s global ischemia starting at the beginning of reperfusion) increased formazan content, reduced LDH release, improved the recovery of the left ventricular developed pressure, maximal rise/fall rate of left ventricular pressure and rate pressure product (left ventricular developed pressure multiplied by heart rate), attenuated the decrease of coronary flow during reperfusion and increased the isolated cell viability. Pretreatment with naltrindole, an antagonist of delta-opioid receptors and calcium-activated potassium channel (KCa) blocker paxilline attenuated the effect of ischemic/hypoxic postconditioning.</p><p><b>CONCLUSION</b>The findings indicate that ischemic postconditioning protects myocardium against ischemia/reperfusion injury via activating delta-opioid receptors and opening KCa.</p>
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Técnicas In Vitro
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Supervivencia Celular
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Ratas Sprague-Dawley
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Receptores Opioides delta
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Biología Celular
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Canales de Potasio Calcio-Activados
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Miocitos Cardíacos
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Poscondicionamiento Isquémico
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Metabolismo
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Miocardio
Tipo de estudio:
Prognostic_studies
Límite:
Animals
Idioma:
Zh
Revista:
Chinese Journal of Applied Physiology
Año:
2008
Tipo del documento:
Article