N-acetylcysteine reduces respiratory burst but augments neutrophil phagocytosis in intensive care unit patients

Objective: The antioxidant N-acetylcysteine (NAC) has been shown to attenuate septic tissue injury. To evaluate whether NAG affects host defense mechanisms in critically ill patients, thus predisposing to increased risk of infection, the current study focuses on neutrophil phagocytotic and burst activity after treatment with NAG. Design: Prospective, randomized, clinical trial. Setting: Twelve-bed operative intensive care unit in a university hospital. Patients: Thirty patients diagnosed with sepsis/systemic inflammatory response syndrome, or multiple trauma. Interventions: Patients were randomly assigned to receive either MAG (n = 15) for 4 days in increasing dosages (day 1: 6 g; day 2: 12 g; days 3 and 4: 18 g) or a mucolytic basis dosage of NAG (3 x 300 mg/day [control]; n = 15), respectively. Measurements and Main Results: Blood samples were taken before NAC high-dose infusion (day 1), after increasing doses of MAG (days 3 and 5) and 4 days after the last high-dose treatment (day 8),. Neutrophil oxidative burst activity after stimulation with Escherichia coli and polymorphonuclear phagocytosis were determined in a flow cytometric assay. Baseline values of polymorphonuclear functions were comparable in both groups, NAC high-dose treatment resulted in a significantly improved phagocytosis activity compared with control patients. In contrast to this, polymorphonuclear burst activity was significantly reduced in the NAG high-dose treated group on day 3, Conclusion: These findings suggest that infusion of NAG in high doses affects granulocyte functions in critically ill patients. Antimicrobial host defense requires the effective sequence of cell adhesion, phagocytosis, and bactericidal respiratory burst. The enhanced phagocytotic activity might be a compensatory mechanism in states of impaired respiratory burst to maintain tissue sterility. For certain mechanisms of disease, the effects observed might be favorable (e.g., ischemia/reperfusion, endothelial cell activation), for others (infection) this might be detrimental.