Cardioprotective effects of NOS and PKC under hemin induced ischemia/reperfusion injury in rat hearts / 中国应用生理学杂志
Chinese Journal of Applied Physiology
;
(6): 180-183, 2007.
Article
in Chinese
| WPRIM
| ID: wpr-253452
ABSTRACT
<p><b>AIM</b>Whether hemin, a heme oxygenase 1 (HO-1) inducer, reduces ischemia/reperfusion injury and whether NO synthase (NOS) and PKC are involved in the cardioprotective effects were investigated in the present study.</p><p><b>METHODS</b>The Langendorff model of isolated rat heart was used. The ventricular function, infarct size, LDH and CK during ischemia/reperfusion period were also observed.</p><p><b>RESULTS</b>(1) After intraperitoneal injection of hemin (50 mg/kg) for 24 h, COHb concentration in rat blood enhanced. He-min preconditioning prevented the increase in LVEDP, decrease in LVDP and +/- dP/dt(max) in the isolated ischemia/reperfusion (ischemia for 30 main and subsequent reperfusion for 2 h) rat hearts. The leakage of LDH and CK in the coronary effluent was significantly declined in hemin-treated rat hearts. And the infarct size was als reduced. (2) By using an inhibitor of NOS NG-nitro-L-arginine methyl ester before the administration of hemin could inhibit the protection induced by hemin. (3) Administration of an inhibitor of protein kinase C chelerythrine (1 mg/kg) before hemin preconditioning could also abolish the cardioprotection induced by hemin.</p><p><b>CONCLUSION</b>These data suggest that the involvement of NO synthase and protein kinase C have been implicated in hemin-induced delayed cardioprotection in isolated rat hearts.</p>
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pharmacology
/
Protein Kinase C
/
Myocardial Reperfusion Injury
/
Rats, Sprague-Dawley
/
Nitric Oxide Synthase
/
NG-Nitroarginine Methyl Ester
/
Heme Oxygenase-1
/
Hemin
/
Metabolism
Limits:
Animals
Language:
Chinese
Journal:
Chinese Journal of Applied Physiology
Year:
2007
Type:
Article
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