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Dose-dependent effects of endotoxin on neurobehavioral functions in humans
Authors:Grigoleit Jan-Sebastian  Kullmann Jennifer S  Wolf Oliver T  Hammes Florian  Wegner Alexander  Jablonowski Stephanie  Engler Harald  Gizewski Elke  Oberbeck Reiner  Schedlowski Manfred
Affiliation:1Institute of Medical Psychology and Behavioral Immunobiology, University of Duisburg-Essen, Essen, Germany;2Department of Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, Essen, Germany;3Department of Cognitive Psychology, Ruhr-University Bochum, Bochum, Germany;4Department of Trauma Surgery, University Hospital Essen, Essen, Germany;University of North Dakota, United States of America
Abstract:Clinical and experimental evidence document that inflammation and increased peripheral cytokine levels are associated with depression-like symptoms and neuropsychological disturbances in humans. However, it remains unclear whether and to what extent cognitive functions like memory and attention are affected by and related to the dose of the inflammatory stimulus. Thus, in a cross-over, double-blind, experimental approach, healthy male volunteers were administered with either placebo or bacterial lipopolysaccharide (LPS) at doses of 0.4 (n = 18) or 0.8 ng/kg of body weight (n = 16). Pro- and anti-inflammatory cytokines, norephinephrine and cortisol concentrations were analyzed before and 1, 1.75, 3, 4, 6, and 24 h after injection. In addition, changes in mood and anxiety levels were determined together with working memory (n-back task) and long term memory performance (recall of emotional and neutral pictures of the International Affective Picture System). Endotoxin administration caused a profound transient physiological response with dose-related elevations in body temperature and heart rate, increases in plasma interleukin (IL)-6, IL-10, tumor necrosis factor (TNF)-α and IL-1 receptor antagonist (IL-1ra), salivary and plasma cortisol, and plasma norepinephrine. These changes were accompanied by dose-related decreased mood and increased anxiety levels. LPS administration did not affect accuracy in working memory performance but improved reaction time in the high-dose LPS condition compared to the control conditon. In contrast, long-term memory performance was impaired selectively for emotional stimuli after administration of the lower but not of the higher dose of LPS. These data suggest the existence of at least two counter-acting mechanisms, one promoting and one inhibiting cognitive performance during acute systemic inflammation.
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