Document Detail


Hypoxia-induced sickness behaviour.
MedLine Citation:
PMID:  17242471     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Sickness behaviour (SB) consists of the set of adaptive responses of the host to severe infections and inflammation. It includes, among others, the thermoregulatory responses such as regulated increase (fever) and/or decrease (anapyrexia) of body temperature (T(b)), decrease of motor activity (lethargy), and loss of appetite (hypophagia) resulting in a transient loss of body weight. It is thought that SB is partially induced by the immune-derived mediators such as cytokines and prostaglandins acting on the central nervous system. It has repeatedly been shown, on the other hand, that severe infections (pneumonia, tissue septicemia) can impair processes of the gases exchange both in the lungs and in distal tissues including brain, which may lead to hypoxia of the affected organs. Therefore, we have tested the hypothesis that hypoxia may also provoke SB. The study was conducted on freely moving biotelemetered mice kept at 28 degrees C ambient and 12/12 h light/dark cycle. We demonstrate that mice exposed for 7 days to hypoxia (11%O(2)) displayed all symptoms of SB. Interleukin-6 deficient mice (IL-6 KO) revealed reduced SB symptoms under hypoxic conditions. Recovery of the hypoxia-exposed mice to a normal rhythm in T(b), motor activity and feeding was unaffected by mepacrine, a phospholipase A(2) blocker. The recovery, however, was significantly impaired by indomethacin, a cyclooxygenase inhibitor. Exposure to hypoxemia resulted in significant elevation of plasma IL-6 in both untreated and treated with lipopolysaccharide (LPS) mice. It inhibited, however, a generation of blood prostaglandins (PGE(2)) in mice. Based on these data we conclude that IL-6 and accumulation of free arachidonic acid in biomembranes contribute to hypoxemia- induced SB.
Authors:
W Kozak; S Wrotek; K Walentynowicz
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of physiology and pharmacology : an official journal of the Polish Physiological Society     Volume:  57 Suppl 8     ISSN:  1899-1505     ISO Abbreviation:  J. Physiol. Pharmacol.     Publication Date:  2006 Nov 
Date Detail:
Created Date:  2007-01-23     Completed Date:  2007-12-06     Revised Date:  2008-05-19    
Medline Journal Info:
Nlm Unique ID:  9114501     Medline TA:  J Physiol Pharmacol     Country:  Poland    
Other Details:
Languages:  eng     Pagination:  35-50     Citation Subset:  IM    
Affiliation:
Department of Immunology, Institute of General and Molecular Biology, Nicolaus Copernicus University, Toruń, Poland. wkozak@biol.uni.torun.pl
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MeSH Terms
Descriptor/Qualifier:
Animals
Anoxia / blood,  enzymology,  physiopathology*
Behavior, Animal / physiology*
Body Temperature / physiology
Body Weight / physiology
Dinoprostone / blood,  physiology*
Eating / physiology
Fever / blood,  enzymology,  physiopathology
Indomethacin / pharmacology
Interleukin-6 / blood,  deficiency,  physiology*
Lipopolysaccharides / pharmacology
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Motor Activity / physiology
Phospholipases A2 / metabolism
Prostaglandin-Endoperoxide Synthases / metabolism
Sick Role*
Specific Pathogen-Free Organisms
Chemical
Reg. No./Substance:
0/Interleukin-6; 0/Lipopolysaccharides; 363-24-6/Dinoprostone; 53-86-1/Indomethacin; EC 1.14.99.1/Prostaglandin-Endoperoxide Synthases; EC 3.1.1.4/Phospholipases A2

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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