Dose-dependent effects of endotoxin on neurobehavioral functions in humans

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...

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Veröffentlicht in:PloS one 2011-12, Vol.6 (12), p.e28330
Hauptverfasser: Grigoleit, Jan-Sebastian, Kullmann, Jennifer S, Wolf, Oliver T, Hammes, Florian, Wegner, Alexander, Jablonowski, Stephanie, Engler, Harald, Gizewski, Elke, Oberbeck, Reiner, Schedlowski, Manfred
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creator Grigoleit, Jan-Sebastian
Kullmann, Jennifer S
Wolf, Oliver T
Hammes, Florian
Wegner, Alexander
Jablonowski, Stephanie
Engler, Harald
Gizewski, Elke
Oberbeck, Reiner
Schedlowski, Manfred
description 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.
doi_str_mv 10.1371/journal.pone.0028330
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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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22164271</pmid><doi>10.1371/journal.pone.0028330</doi><tpages>e28330</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
ispartof PloS one, 2011-12, Vol.6 (12), p.e28330
issn 1932-6203
1932-6203
language eng
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subjects Adult
Age
Analysis
Animal cognition
Anxiety
Attention
Bacteria
Behavior
Behavior - drug effects
Biology
Blood
Body Mass Index
Body Temperature
Body Weight
Brain
Clinical trials
Cognitive ability
Cognitive tasks
Cortisol
Cross-Over Studies
Cytokines
Depression (Mood disorder)
Dosage
Dosage and administration
Dose-Response Relationship, Drug
Double-Blind Method
Drug dosages
Emotions
Endotoxins - metabolism
Endotoxins - pharmacology
Gender differences
Glucocorticoids
Heart Rate
Hormones
Humans
Inflammation
Inhibition (psychology)
Interleukin 1
Interleukin 1 receptor antagonist
Interleukin 1 Receptor Antagonist Protein - metabolism
Interleukin 10
Interleukin-10 - blood
Interleukin-6 - blood
Lipopolysaccharides
Lipopolysaccharides - metabolism
Long term memory
Male
Medical research
Medicine
Memory
Mental depression
Mitogens
Models, Neurological
Mood
Neurosciences
Norepinephrine
Physiological aspects
Pictures
Placebos
Psychology
Reaction time
Reaction time task
Rodents
Short term memory
Social research
Surgery
Tumor Necrosis Factor-alpha - metabolism
Tumor necrosis factor-TNF
Tumor necrosis factor-α
title Dose-dependent effects of endotoxin on neurobehavioral functions in humans
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