Literature DB >> 20558166

Distribution and time course of corticosterone excretion in faeces and urine of female mice with varying systemic concentrations.

Otto Kalliokoski1, Jann Hau, Kirsten R Jacobsen, Camilla Schumacher-Petersen, Klas S P Abelson.   

Abstract

Quantification of corticosterone metabolites excreted in faeces and urine is increasingly being used for assessment of preceding corticosterone concentrations in the circulation. This is a promising approach to non-invasive stress assessment in laboratory rodents. It is however unknown whether the proportions of corticosterone metabolites excreted in faeces and urine may differ, depending on the concentration of corticosterone in blood. This uncertainty undermines the applicability of urinary and faecal corticosterone metabolite measurements as biomarkers for stress. Therefore, the terminal distribution and time course of corticosterone excretion, after intravenous injection of varying corticosterone concentrations, was investigated in female mice. Female BALB/c mice excreted 60% of all corticosterone in the urine with an approximate delay of 5h from tail vein administration. The remaining 40% were excreted in faeces, with an approximate delay of 9h from administration. The faecal/urinary excretion ratio, as well as time course of excretion, remained unaltered by administration of various doses of corticosterone covering the entire physiological range of serum corticosterone. Although currently untested for other strains of mice and species of animals, these findings add credence to the utility of faecal and urinary corticosterone as non-invasive biomarkers for physiological stress. Copyright (c) 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20558166     DOI: 10.1016/j.ygcen.2010.06.003

Source DB:  PubMed          Journal:  Gen Comp Endocrinol        ISSN: 0016-6480            Impact factor:   2.822


  4 in total

1.  Manual versus automated blood sampling: impact of repeated blood sampling on stress parameters and behavior in male NMRI mice.

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Journal:  Lab Anim       Date:  2014-06-23       Impact factor: 2.471

2.  Forced treadmill exercise can induce stress and increase neuronal damage in a mouse model of global cerebral ischemia.

Authors:  Martina Svensson; Philip Rosvall; Antonio Boza-Serrano; Emelie Andersson; Jan Lexell; Tomas Deierborg
Journal:  Neurobiol Stress       Date:  2016-09-09

3.  Mice do not habituate to metabolism cage housing--a three week study of male BALB/c mice.

Authors:  Otto Kalliokoski; Kirsten R Jacobsen; Huda S Darusman; Trine Henriksen; Allan Weimann; Henrik E Poulsen; Jann Hau; Klas S P Abelson
Journal:  PLoS One       Date:  2013-03-07       Impact factor: 3.240

4.  Nonsurgical embryo transfer device compared with surgery for embryo transfer in mice.

Authors:  Kendra H Steele; James M Hester; Barbara J Stone; Kimberly M Carrico; Brett T Spear; Angelika Fath-Goodin
Journal:  J Am Assoc Lab Anim Sci       Date:  2013-01       Impact factor: 1.706

  4 in total

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