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Bioactive Sphingolipids, Complement Cascade, and Free Hemoglobin Levels in Stable Coronary Artery Disease and Acute
T Jadczyk1,2, K Baranski3, M Syzdol1
1Division of Cardiology and Structural Heart Diseases, Medical University of Silesia, Ziołowa 45-47, Katowice, Poland.
Insights
Inflammatory responses in acute myocardial infarction (AMI) and coronary artery bypass graft (CABG) surgery differ. Complement cascade fragments and free hemoglobin levels varied between AMI and CABG patients, impacting bioactive sphingolipid levels.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Biochemistry
Background:
- Acute myocardial infarction (AMI) and coronary artery bypass graft (CABG) surgery trigger sterile inflammation.
- The complement cascade (CC) and bioactive sphingolipids (BS) are implicated in these inflammatory processes.
Purpose of the Study:
- To compare plasma levels of CC cleavage fragments (C3a, C5a, C5b9), sphingosine (SP), sphingosine-1-phosphate (S1P), and free hemoglobin (fHb).
- To evaluate these markers in patients with AMI undergoing primary percutaneous coronary intervention (pPCI) versus stable coronary artery disease (SCAD) patients undergoing CABG.
Main Methods:
- Plasma samples were collected from 22 AMI patients, 7 CABG patients, and 8 healthy controls at multiple time points post-intervention.
- High-performance liquid chromatography (HPLC) measured SP and S1P.
- High-sensitivity ELISA and spectrophotometry quantified CC fragments and fHb, respectively.
Main Results:
- CABG patients exhibited higher plasma levels of C3a and C5b9, but lower SP and S1P compared to AMI patients.
- CC factor levels remained stable in both groups within 48 hours.
- SP and S1P decreased over 48 hours in AMI patients, while remaining stable post-CABG.
- Free hemoglobin levels were significantly higher at 24 and 48 hours post-pPCI compared to CABG.
Conclusions:
- The inflammatory response following AMI and CABG surgery exhibits distinct patterns.
- Differences were observed in the release of sphingolipids, free hemoglobin, and complement cascade fragments between the two procedures.
Background:
Acute myocardial infarction (AMI) and coronary artery bypass graft (CABG) surgery are associated with a pathogen-free inflammatory response (sterile inflammation). Complement cascade (CC) and bioactive sphingolipids (BS) are postulated to be involved in this process.
Aim:
The aim of this study was to evaluate plasma levels of CC cleavage fragments (C3a, C5a, and C5b9), sphingosine (SP), sphingosine-1-phosphate (S1P), and free hemoglobin (fHb) in AMI patients treated with primary percutaneous coronary intervention (pPCI) and stable coronary artery disease (SCAD) undergoing CABG.
Patients And Methods:
The study enrolled 37 subjects (27 male) including 22 AMI patients, 7 CABG patients, and 8 healthy individuals as the control group (CTRL). In the AMI group, blood samples were collected at 5 time points (admission to hospital, 6, 12, 24, and 48 hours post pPCI) and 4 time points in the CABG group (6, 12, 24, and 48 hours post operation). SP and S1P concentrations were measured by high-performance liquid chromatography (HPLC). Analysis of C3a, C5a, and C5b9 levels was carried out using high-sensitivity ELISA and free hemoglobin by spectrophotometry.
Results:
The plasma levels of CC cleavage fragments (C3a and C5b9) were significantly higher, while those of SP and S1P were lower in patients undergoing CABG surgery in comparison to the AMI group. In both groups, levels of CC factors showed no significant changes within 48 hours of follow-up. Conversely, SP and S1P levels gradually decreased throughout 48 hours in the AMI group but remained stable after CABG. Moreover, the fHb concentration was significantly higher after 24 and 48 hours post pPCI compared to the corresponding postoperative time points. Additionally, the fHb concentrations increased between 12 and 48 hours after PCI in patients with AMI.
Conclusions:
Inflammatory response after AMI and CABG differed regarding the release of sphingolipids, free hemoglobin, and complement cascade cleavage fragments.
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