Cholinergic status modulations in human volunteers under acute inflammation

• Published in: Journal of molecular medicine (Berlin, Germany) Vol. 85; no. 11; pp. 1239 - 1251
• Main Authors: OFEK, Keren, KRABBE, Karen S, EVRON, Tama, DEBECCO, Meir, NIELSEN, Anders R, BRUNNSGAAD, Helle, YIRMIYA, Raz, SOREQ, Hermona, PEDERSEN, Bente K
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.11.2007; Springer Nature B.V
• Subjects: Acetylcholinesterase - genetics; Acetylcholinesterase - metabolism; Acute Disease; Adult; Aged; Attention - drug effects; Biological and medical sciences; Biomarkers - metabolism; Butyrylcholinesterase - metabolism; Choline - metabolism; Endotoxins - pharmacology; General aspects; Humans; Immunity, Innate - drug effects; Inflammation - metabolism; Interleukin-6 - administration & dosage; Interleukin-6 - pharmacology; Male; Medical sciences; Memory - drug effects; Recombinant Proteins - administration & dosage; Recombinant Proteins - pharmacology; Up-Regulation - drug effects; Human; Enzyme; Acute; Volunteer; Cytokine; Esterases; Inflammation; Paraoxonase; Acetylcholinesterase; Carboxylic ester hydrolases; Medicine; Phosphoric triester hydrolases; Acetylcholinesterase . Butyrylcholinesterase; Modulation; Hydrolases; Aryldialkylphosphatase; Human . Cytokines
• ISSN: 0946-2716; 1432-1440
• DOI: 10.1007/s00109-007-0226-x

Cholinergic Status, the total soluble circulation capacity for acetylcholine hydrolysis, was tested for putative involvement in individual variabilities of the recruitment of immune cells in response to endotoxin challenge. Young (average age 26) and elderly (average age 70) volunteers injected with either Escherichia coli endotoxin or saline on two different occasions were first designated Enhancers and Suppressors if they showed increase or decrease, respectively, in plasma acetylcholinesterase (AChE) activity 1.5 h after endotoxin administration compared to saline. Enhancers showed significant co-increases in plasma butyrylcholinesterase (BChE) and paraoxonase (PON1) activities, accompanied by rapid recovery of lymphocyte counts. Young Enhancers alone showed pronounced post-exposure increases in the pro-inflammatory cytokine interleukin-6 (IL-6), and upregulation of the normally rare, stress-induced AChE-R variant, suggesting age-associated exhaustion of the cholinergic effects on recruiting innate immune reactions to endotoxin challenge. Importantly, IL-6 injected to young volunteers or administered in vitro to primary mononuclear blood cells caused upregulation of AChE, but not BChE or PON1, excluding it from being the sole cause for this extended response. Interestingly, Suppressors but not Enhancers showed improved post-exposure working memory performance, indicating that limited cholinergic reactions may be beneficial for cognition. Our findings establish Cholinergic Status modulations as early facilitators and predictors of individual variabilities in the peripheral response to infection.