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Remifentanil은 흰쥐의 국소 허혈-재관류 모델에서 심근 보호 효과가 있는가?Dose remifentanil have a myocardial protective effect against a regional ischemia-reperfusion injury in an in vivo rat heart model?

Other Titles
Dose remifentanil have a myocardial protective effect against a regional ischemia-reperfusion injury in an in vivo rat heart model?
Authors
신일우조만석장인석손주태이헌근정영균
Issue Date
2009
Publisher
대한마취통증의학회
Keywords
Heart; In vivo; Ischemia-reperfusion injury; Remifentanil
Citation
Korean Journal of Anesthesiology, v.57, no.2, pp 190 - 194
Pages
5
Indexed
KCI
Journal Title
Korean Journal of Anesthesiology
Volume
57
Number
2
Start Page
190
End Page
194
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/26787
ISSN
2005-6419
2005-7563
Abstract
Background: It is known that some opioids protect the myocardial tissue from myocardial ischemia-reperfusion (I/R) injury. The aim of this study was to investigate whether remifentanil, at a clinically relevant concentration that’s during the peri-ischemic period, has a protective effect against a regional I/R injury in an in vivo rat heart model. Methods: Rats were subjected to 25 minutes of coronary artery occlusion and this was followed by 24 hours of reperfusion. A microcatheter was advanced into the left ventricle and the hemodynamic function was evaluated after 24 hours of reperfusion. The infarct size was determined by triphenyltetrazolium staining. The serum level of cardiac troponin-I (cTnI) was determined by ELISA (enzyme-linked immunosorbent assay). Results: Remifentanil administration during the peri-ischemic period didn’t show any identifiable protective effects for the hemodynamic function or to reduce the infarct size. In the control group, the peak rate of the ventricular pressure increase (+dP/dtmax) (P < 0.05) and the peak rate of the intraventricular pressure decline (−dP/dtmax P < 0.05) were significantly decreased as compared to those values for the sham group. In the remifentanil group, the +dP/dtmax and −dP/dtmax were not improved compared to those values of the control group. The infarct size was 45.6% of the area at risk in the control group, and the infarct size was reduced by administration of remifentanil to 43.2% in the remifentanil group. The I/R-induced serum level of cTn-I was not reduced by remifentanil infusion during the peri-ischemic period. Conclusions: Remifentanil, at a clinically relevant concentration that’s infused during the peri-ischemic period, has no myocardial protective effect after regional myocardial I/R injury in an in vivo rat heart model.
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