Literature DB >> 17433456

The rate of behavioral tolerance development to repeated lipopolysaccharide treatments depends upon the time of injection during the light-dark cycle: a multivariable examination of locomotor activity.

Andrew E Franklin1, Christopher G Engeland, Martin Kavaliers, Klaus-Peter Ossenkopp.   

Abstract

Recent evidence suggests that sickness behaviors following lipopolysaccharide (LPS)-treatment may be modulated by environmental factors such as the light-dark (LD) cycle. The present study characterized LPS-induced hypoactivity and behavioral tolerance development across individual phases of the light-dark cycle and the transitions between phases. On days 1, 4 and 7, male rats were treated with LPS (200microg/kg i.p.) or saline 30min prior to the onset of either the dark period (dark-tested group) or the light period (light-tested group). Following treatment, rats were placed in non-novel automated open-fields where various aspects of locomotor activity were monitored for 16h. On day 1, LPS-treated rats in both the dark and light tested groups showed significant hypoactivity. However, temporal differences in the onset of hypoactivity were observed between the groups. In dark tested animals significant hypoactivity started 60min after LPS treatment and continued until the light period when hypoactivity was diminished. In contrast, the light tested LPS-treated animals did not exhibit a prolonged period of hypoactivity until the transition between the light and dark periods, 750min following LPS injection. On days 4 and 7, light tested animals showed complete tolerance to LPS as evidenced by the absence of significant activity reductions, whereas dark tested animals continued to show significant periods of hypoactivity. These results indicate that there are day-night differences in both the initial LPS-induced hypoactivity response as well as behavioral tolerance development. The rate of tolerance development to LPS may be a critical factor to survival and the prevention of sepsis, as organisms are repeatedly exposed to pathogens across the life cycle.

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Year:  2007        PMID: 17433456     DOI: 10.1016/j.bbr.2007.03.021

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  5 in total

1.  How does immune challenge inhibit ingestion of palatable food? Evidence that systemic lipopolysaccharide treatment modulates key nodal points of feeding neurocircuitry.

Authors:  Su-Mi Park; Ron P A Gaykema; Lisa E Goehler
Journal:  Brain Behav Immun       Date:  2008-06-17       Impact factor: 7.217

2.  Sex-dependent effects of neonatal inflammation on adult inflammatory markers and behavior.

Authors:  A C Kentner; S A McLeod; E F Field; Q J Pittman
Journal:  Endocrinology       Date:  2010-04-14       Impact factor: 4.736

3.  Sex-specific social regulation of inflammatory responses and sickness behaviors.

Authors:  Jason R Yee; Brian J Prendergast
Journal:  Brain Behav Immun       Date:  2010-03-17       Impact factor: 7.217

4.  Impaired leukocyte trafficking and skin inflammatory responses in hamsters lacking a functional circadian system.

Authors:  Brian J Prendergast; Erin J Cable; Priyesh N Patel; Leah M Pyter; Kenneth G Onishi; Tyler J Stevenson; Norman F Ruby; Sean P Bradley
Journal:  Brain Behav Immun       Date:  2013-03-07       Impact factor: 7.217

Review 5.  Sickness behaviour pushed too far--the basis of the syndrome seen in severe protozoal, bacterial and viral diseases and post-trauma.

Authors:  Ian A Clark; Alison C Budd; Lisa M Alleva
Journal:  Malar J       Date:  2008-10-14       Impact factor: 2.979

  5 in total

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