High glucose impairs superoxide production from isolated blood neutrophils

• Published in: Intensive care medicine Vol. 29; no. 4; pp. 642 - 645
• Main Authors: PERNER, A, NIELSEN, S. E, RASK-MADSEN, J
• Format: Journal Article
• Language: English
• Published: Heidelberg Springer 01.04.2003; Berlin Springer Nature B.V
• Subjects: Analysis of Variance; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Biological and medical sciences; Cells, Cultured; Dehydroepiandrosterone - pharmacology; Emergency and intensive care: metabolism and nutrition disorders. Enteral and parenteral nutrition; Glucose - pharmacology; Humans; Intensive care medicine; Medical sciences; Neutrophils - drug effects; Neutrophils - metabolism; Superoxides - metabolism; Human; Glucose-6-phosphate 1-dehydrogenase; Reactive oxygen species; Healthy subject; Enzyme; Neutrophils; Glucose; Antimicrobial agent; Extracellular space; NADPH peroxidase; Cytochrome c; In vivo; Hyperglycemia; Hyperoxides; Peroxidases; Superoxides; Oxidoreductases; Neutrophil; Glucose Glucose- phosphate dehydrogenase; Quantitative analysis; Phagocyte
• ISSN: 0342-4642; 1432-1238
• DOI: 10.1007/s00134-002-1628-4

Superoxide (O(2)(-)), a key antimicrobial agent in phagocytes, is produced by the activity of NADPH oxidase. High glucose concentrations may, however, impair the production of O(2)(-) through inhibition of glucose-6-phosphate dehydrogenase (G6PD), which catalyzes the formation of NADPH. This study measured the acute effects of high glucose or the G6PD inhibitor dehydroepiandrosterone (DHEA) on the production of O(2)(-) from isolated human neutrophils. Laboratory studies of short-term cultures of neutrophil granulocytes. Healthy subjects. Neutrophils were isolated from peripheral blood and incubated for 1 h in Krebs-Ringer buffer containing 5, 10, or 25 mM glucose, 5 mM glucose with 0, 5, or 20 mM mannitol, or 5 mM glucose with 0, 1, 10, or 100 micro M DHEA. O(2)(-) production was induced by N-formyl-methionyl-leucyl-phenylalanine and measured by the cytochrome c reduction assay. Potential scavenging of O(2)(-) by glucose, mannitol, or DHEA was assessed in a cell free system using the pyrogallol assay. Incubation of neutrophils with glucose dose-dependently reduced O(2)(-) production, which was 50% decreased at 25 mM glucose. Also DHEA reduced the production of O(2)(-) dose-dependently, whereas production rates were unaffected by mannitol. Neither glucose, mannitol, nor DHEA scavenged O(2)(-). High extracellular glucose concentrations acutely reduce O(2)(-) production from activated neutrophils possibly through inhibition of G6PD. If this occurs in vivo, microbial killing by neutrophils may be impaired during acute hyperglycemia, as observed after major surgery, trauma, or severe infection.