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The effects of propofol on neutrophil function, lipid peroxidation and inflammatory response during elective coronary
T B Corcoran1, A Engel, H Sakamoto
1Department of Anaesthesia and Intensive Care Medicine, Cork University/Mercy Hospitals and University College Cork, Cork City, Ireland. mascor@bigpond.net.au
Insights
Propofol reduces reperfusion injury and inflammation during coronary artery bypass grafting (CABG) in patients with impaired heart function. This antioxidant effect may protect against oxidative stress and inflammatory responses post-surgery.
Area of Science:
- Cardiology
- Anesthesiology
- Biochemistry
Background:
- Coronary artery bypass grafting (CABG) with cardiopulmonary bypass causes significant reperfusion injury and inflammation, particularly in patients with compromised myocardial function.
- Propofol, an anesthetic agent, possesses antioxidant properties that may mitigate these adverse effects.
Purpose of the Study:
- To investigate the efficacy of propofol in attenuating reperfusion injury and systemic inflammation in patients with impaired left ventricular function undergoing CABG.
- To assess the impact of propofol on oxidative stress markers and inflammatory mediators post-CABG.
Main Methods:
- A randomized controlled trial involving 27 patients with impaired left ventricular function undergoing CABG.
- Patients received either target-controlled infusion propofol or saline from before aortic cross-clamp release until 4 hours post-reperfusion.
- Measurements included Troponin-I, urinary 8-epi PGF-2alpha isoprostane, malondialdehyde (MDA), Interleukin-6 (IL-6), IL-8, IL-10, and leukocyte function.
Main Results:
- Propofol significantly reduced coronary sinus and systemic malondialdehyde (MDA) concentrations post-reperfusion.
- Increases in Interleukin-6 (IL-6) were significantly lower in the propofol group compared to the saline group 4 hours post-reperfusion.
- While Interleukin-10 (IL-10) levels decreased post-reperfusion, they remained higher in the propofol group than the control group.
Conclusions:
- Propofol effectively attenuates free-radical-mediated lipid peroxidation in patients undergoing CABG with impaired myocardial function.
- Propofol demonstrates a systemic anti-inflammatory effect in this patient population, reducing key inflammatory markers post-surgery.
Background:
Coronary artery bypass grafting (CABG) with cardiopulmonary bypass elicits a potent reperfusion injury and inflammatory response, more intense in patients with impaired myocardial function. Propofol has antioxidant properties which may attenuate such a response.
Methods:
In total, 27 patients with impaired left ventricular function undergoing CABG were randomly allocated to receive either target-controlled infusion propofol (P) or saline (S) immediately before aortic cross-clamp release until 4 h after reperfusion. Troponin-I, Urinary 8-epi PGF-2alpha isoprostane, coronary sinus and systemic malondialdehyde concentrations, Interleukin-6 (IL-6), -8 and -10 concentrations and leucocytes function studies (neutrophil respiratory burst, phagocytosis, CD-11b and CD-18 expression) were measured.
Results:
Propofol decreased MDA coronary sinus concentration at 1, 3 and 5 min after reperfusion (P<0.01); 60 min after reperfusion a significant difference between the two groups in systemic MDA concentrations was also seen. IL-6 concentration increases were significantly greater in Group S than Group P, 4 h after reperfusion [1118 (1333) pg ml(-1) vs 228 (105) pg ml(-1), P<0.01]. Serum IL-8 concentrations did not increase significantly in either group. Compared with baseline values IL-10 concentrations decreased after reperfusion but the values were higher in the propofol group than in the control group [22 (16) vs 11 (4) pg ml(-1), P<0.05]. No difference in leucocyte function or urinary isoprostane concentrations was demonstrated.
Conclusion:
Propofol attenuates free-radical-mediated lipid peroxidation and systemic inflammation in patients with impaired myocardial function undergoing CABG.
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