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Effects of granulocyte-colony stimulating factor on the polymorphonuclear leukocyte activity and the course of sepsis
Gunay Gurleyik1, Gulderen Yanikkaya, Emin Gurleyik
1Department of Surgery, Haydarpasa Numune Teaching and Research Hospital, Istanbul, Turkey.
Purpose:
Polymorphonuclear leucocytes (PML) play an essential role in the host immune response to severe infections. The effects of granulocyte-colony stimulating factor (G-CSF) on the PML immune functions during serious abdominal infection and course of sepsis, and on the survival in rats with peritonitis are the main subjects of this study.
Methods:
The first phase of the study was carried out on 30 Wistar-albino rats equally divided into three groups; Group 1 (control) sham laparotomy; Group 2 (peritonitis); and Group 3 (peritonitis+G-CSF) with fecal peritonitis created by a cecal puncture. At postoperative hours 3, 12, and 24, 0.5 ml normal saline was injected subcutaneously in groups 1 and 2, and 0.5 ml solution containing 50 microg/kg of G-CSF in group 3. The phagocytic and chemotactic activities of neutrophils and monocytes were evaluated by a flow cytometry analysis. The plasma lactate concentrations were assessed as a marker of tissue perfusion during sepsis. The second phase was a survival analysis, which was observed during 10 days on 20 rats equally divided into two groups; group 1 (peritonitis) and group 2 (peritonitis+G-CSF). 0.5 ml normal saline in group 1 and 50 microg/kg of G-CSF in group 2 was injected subcutaneously at the 3rd hour and twice daily.
Results:
Both the neutrophil- (1.636 vs 2.236) and monocyte-related (1.789 vs 2.465) phagocytic activities significantly (P < 0.001) improved after the G-CSF administration in the rats with peritonitis. In addition, the G-CSF treatment significantly (P < 0.0014) improved the chemotactic activity (1.18 vs 2.75) of neutrophils, and partly supported (P < 0.0952) the chemotactic activity (1.69 vs 2.37) of monocytes. The plasma lactate level (1.86 vs 4.9 mmol/l) was significantly (P < 0.0001) increased after septic changes due to experimental peritonitis. On the other hand, the lactate concentration was significantly (P < 0.001) decreased (4.9 vs 2.63 mmol/l) after the G-CSF administration. The survival was 20% at the 4th day and 0 at the 6th day in peritonitis, and 90% at the 4th day (P = 0.0055) and 80% at the 6th day (P = 0.0007) days in the peritonitis+G-CSF groups.
Conclusion:
G-CSF enhances the immune functions of neutrophils and monocytes. The increased activities of these cells have a beneficial effect on the enhancement of the host immune response during severe infections. The improved immune function of PML due to the G-CSF treatment thus ameliorates the survival and the courses of sepsis, which is also defined by tissue perfusion and the cellular oxygen balance, which is affected by septic changes.
Insights
Granulocyte-colony stimulating factor (G-CSF) significantly boosts immune cell function in rats with peritonitis, improving survival rates. This G-CSF treatment enhances neutrophil and monocyte activities, crucial for combating severe infections.
Area of Science:
- Immunology
- Critical Care Medicine
- Pharmacology
Background:
- Polymorphonuclear leukocytes (PML) are vital for immune response during severe infections.
- Sepsis and peritonitis represent critical conditions where immune function is compromised.
- Granulocyte-colony stimulating factor (G-CSF) is known to influence leukocyte function.
Purpose of the Study:
- To investigate the impact of G-CSF on polymorphonuclear leukocyte (PML) immune functions in rats with experimental peritonitis.
- To evaluate the effect of G-CSF on the course of sepsis and survival rates in a peritonitis model.
- To assess G-CSF's influence on neutrophil and monocyte phagocytic and chemotactic activities.
Main Methods:
- A peritonitis model was induced in Wistar-albino rats via cecal puncture.
- Rats were divided into control, peritonitis, and peritonitis+G-CSF groups.
- Neutrophil and monocyte functions (phagocytosis, chemotaxis) were assessed using flow cytometry; plasma lactate levels were measured; survival analysis was conducted over 10 days.
Main Results:
- G-CSF significantly enhanced neutrophil and monocyte phagocytic activity (P < 0.001) and neutrophil chemotactic activity (P < 0.0014).
- G-CSF partially improved monocyte chemotactic activity (P < 0.0952) and significantly reduced plasma lactate levels (P < 0.001), indicating improved tissue perfusion.
- Survival rates were significantly higher in the G-CSF treated group (80-90%) compared to the peritonitis-only group (0-20%) (P = 0.0007).
Conclusions:
- G-CSF administration enhances the immune functions of neutrophils and monocytes during experimental peritonitis.
- Improved leukocyte function correlates with better host immune response, ameliorating sepsis progression and improving survival.
- G-CSF treatment positively impacts tissue perfusion and cellular oxygen balance, crucial factors in managing sepsis.
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