Quantitative effects of diet on fecal corticosterone metabolites in two strains of laboratory mice

Otto Kalliokoski, Kirsten Rosenmaj Jacobsen, Anne Charlotte Teilmann, Jann Hau, Klas Abelson

20 Citations (Scopus)

Abstract

The analysis of glucocorticoids excreted in feces is becoming a widespread technique for determining animal wellbeing in a wide variety of settings. In the present study an extraction protocol and an ELISA assay for quantifying fecal corticosterone metabolites (FCM) in BALBIc and C57bl/6 mice were validated. Lower ratios of solvent (ethanoi) to mass of fecal sample were found to be sufficient in extracting FCM compared to what has been reported previously. Feeding mice a high energy diet, high in fat content (60% of calories from fat), significantly lowered the FCM excretion, approximately halving the FCM output. This diet also reduced the fecal mass voided to approximately a third of that of the regular diet. The two reductions were not correlated. A difference in defecation pattern was seen between the two strains, with the BALBIc mice having a more pronounced diurnal rhythm compared to the C57bl/6 mice. Furthermore, throughout the experiment, the C57bl/6 mice excreted significantly higher levels of FCM compared to the BALBIc mice. The mice were also challenged with synthetic adrenocorticotropic hormone (ACTH) and dexamethasone (DEX). The effect of the challenges could readily be detected, but had a considerably lesser impact on data than did the difference in diet. The study demonstrates some problematic consequences of expressing FCM excretion as a measure of fecal dry mass. The study also serves to emphasize the caution that must be exercised when interpreting FCM excretion in conjunction with an uncontrolled or varied diet, or perturbations of gastro-intestinal functioning.

Original languageEnglish
JournalIn Vivo
Volume26
Issue number2
Pages (from-to)213-221
Number of pages9
ISSN0258-851X
Publication statusPublished - Mar 2012

Fingerprint

Dive into the research topics of 'Quantitative effects of diet on fecal corticosterone metabolites in two strains of laboratory mice'. Together they form a unique fingerprint.

Cite this