AGE-modified albumin containing infusion solutions boosts septicaemia and inflammation in experimental peritonitis

• Published in: Journal of leukocyte biology Vol. 86; no. 3; pp. 589 - 597
• Main Authors: Humpert, Per M., Lukic, Ivan K., Thorpe, Suzanne R., Hofer, Stefan, Awad, Ezzat M., Andrassy, Martin, Deemer, Elizabeth K., Kasper, Michael, Schleicher, Erwin, Schwaninger, Markus, Weigand, Markus A., Nawroth, Peter P., Bierhaus, Angelika
• Format: Journal Article
• Language: English
• Published: United States Society for Leukocyte Biology 01.09.2009; The Society for Leukocyte Biology
• Subjects: advanced glycation endproducts; Age; Albumin; Animal models; Animals; Aorta - cytology; Cattle; Cells, Cultured; Clinical trials; colloid; Disease Models, Animal; Endothelial Cells - metabolism; Endothelium, Vascular - cytology; fluid resuscitation; Gene expression; Glycation End Products, Advanced - metabolism; Immunoglobulins; Inflammation; Inflammation - etiology; Inflammation - metabolism; Infusions, Intravenous; Lethality; Leukocytes; Mice; Mice, Inbred C57BL; Mice, Knockout; Mortality; NF-B protein; Osmotic pressure; Peritoneum; Peritonitis; Peritonitis - pathology; Post-transcription; Primary Research; RAGE; Sepsis; Sepsis - etiology; Sepsis - genetics; Sepsis - metabolism; Serum Albumin - metabolism; Solutions; Transcription factors; Transfection
• ISSN: 0741-5400; 1938-3673
• DOI: 10.1189/jlb.1008646

Advanced glycation endproducts (AGEs) act as potential contaminants of infusion solutions boosting inflammation in experimental sepsis. HSA preparations for i.v. use are administered in critically ill patients. Although increasing intravascular osmotic pressure seems to be a pathophysiologically orientated treatment, clinical trials do not indicate a benefit for mortality in HSA–treated patients. Instead, there is evidence for inflammatory reactions upon infusion of different HSA batches. A neglected issue concerning the safety and quality of these therapeutics is processing–related post–transcriptional protein modifications, such as AGEs. We therefore tested the hypothesis that commercially available infusion solutions contain AGEs and studied whether these protein modifications influence outcome and inflammation in a murine model of sepsis induced by CLP. Screening of different HSA and Ig preparations in this study revealed an up to approximate tenfold difference in the amount of AGE modifications. Application of clinically relevant concentrations of CML–modified HSA in CLP led to increased inflammation and enhanced mortality in wild–type mice but not in mice lacking the RAGE. Lethality was paralleled by increased activation of the proinflammatory transcription factor NF–κB, NF–κB–dependent gene expression, and infiltration of inflammatory cells in the peritoneal cavity. This study implies that infusion solutions containing a high load of the AGE–modified protein have the potential to activate RAGE/NF–κB–mediated inflammatory reactions, causing increased mortality in experimental peritonitis.