쥐의 국소 허혈 재관류 모델에서 허혈 전후에 투여한 Propofol의 심근 보호 효과The effect of propofol on myocardial protection after regional ischemia-reperfusion injury in an in vivo rat heart model
- Other Titles
- The effect of propofol on myocardial protection after regional ischemia-reperfusion injury in an in vivo rat heart model
- Authors
- 신일우; 임병원; 정영석; 이효민; 손주태; 이헌근; 정영균
- Issue Date
- 2008
- Publisher
- 대한마취통증의학회
- Keywords
- heart; in vivo; ischemia-reperfusion injury; propofol.; heart; in vivo; ischemia-reperfusion injury; propofol.
- Citation
- Korean Journal of Anesthesiology, v.53, no.3, pp 338 - 343
- Pages
- 6
- Indexed
- KCI
- Journal Title
- Korean Journal of Anesthesiology
- Volume
- 53
- Number
- 3
- Start Page
- 338
- End Page
- 343
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/27805
- ISSN
- 2005-6419
2005-7563
- Abstract
- Background: It is known that propofol protects myocardium against a global ischemia-reperfusion injury in the isolated rat heart model. The aim of this study was to investigate whether propofol, at a clinically relevant concentration infused during the peri-ischemic period, also provides a protective effect against a regional myocardial ischemia-reperfusion injury in vivo.
Methods: Rats were subjected to 25 minutes of coronary artery occlusion followed by 24 hours of reperfusion. Propofol or intralipid was administrated during 35 minutes starting 5 minutes before the onset of ischemia until 5 minutes after the onset of reperfusion. A micromanometer catheter was advanced into the left ventricle and the hemodynamic function was evaluated. The infarct size was determined by triphenyltetrazolium staining after 24 hours of reperfusion.
Results: Propofol administration during the peri-ischemic period demonstrated protective effects on hemodynamic function and infarct size reduction. In the control group, the peak rate of the ventricular pressure increase (+dP/dtmax)(P = 0.0001) and the peak rate of the intraventricular pressure decline (−dP/dtmax)(P = 0.0001) were significantly decreased compared to the sham group. In the propofol group, the +dP/dtmax (P = 0.003) and −dP/dtmax (P = 0.002) were significantly improved compared to the control group. The infarct size was 47.6% of the area at risks in the control group, and was reduced markedly by administration of propofol during the peri-ischemic period to 26.2% in the propofol group (P = 0.004).
Conclusions: Propofol, at a clinically relevant concentration infused during the peri-ischemic period, have protective effect after regional myocardial ischemia-reperfusion injury in an in vivo rat heart model
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