Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive Techniques

Testosterone is the main reproductive hormone in male vertebrates and conventional methods to measure testosterone rely on invasive blood sampling procedures. Here, we aimed to establish a non-invasive alternative by assessing testosterone metabolites (TMs) in fecal and urinary samples in mice. We p...

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Main Authors: Kerstin E. Auer, Marius Kußmaul, Erich Möstl, Katharina Hohlbaum, Thomas Rülicke, Rupert Palme
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Animals
Subjects:
Online Access:https://www.mdpi.com/2076-2615/10/1/165
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author Kerstin E. Auer
Marius Kußmaul
Erich Möstl
Katharina Hohlbaum
Thomas Rülicke
Rupert Palme
author_facet Kerstin E. Auer
Marius Kußmaul
Erich Möstl
Katharina Hohlbaum
Thomas Rülicke
Rupert Palme
author_sort Kerstin E. Auer
collection DOAJ
description Testosterone is the main reproductive hormone in male vertebrates and conventional methods to measure testosterone rely on invasive blood sampling procedures. Here, we aimed to establish a non-invasive alternative by assessing testosterone metabolites (TMs) in fecal and urinary samples in mice. We performed a radiometabolism study to determine the effects of daytime and sex on the metabolism and excretion pattern of radiolabeled TMs. We performed physiological and biological validations of the applied EIA to measure TMs and assessed diurnal fluctuations in TM excretions in male and female mice and across strains. We found that males excreted significantly more radiolabeled TMs via the feces (59%) compared to females (49.5%). TM excretion patterns differed significantly between urinary and fecal samples and were affected by the daytime of &#179;H-testosterone injection. Overall, TM excretion occurred faster in urinary than fecal samples. Peak excretion of fecal TMs occurred after 8 h when animals received the <sup>3</sup>H-testosterone in the morning, or after 4 h when they received the <sup>3</sup>H-testosterone injection in the evening. Daytime had no effect on the formed TMs; however, males and females formed different types of TMs. As expected, males showed higher fecal TM levels than females. Males also showed diurnal fluctuations in their TM levels but we found no differences in the TM levels of C57BL/6J and B6D2F1 hybrid males. Finally, we successfully validated our applied EIA (measuring 17&#946;-hydroxyandrostane) by showing that hCG (human chorionic gonadotropin) administration increased TM levels, whereas castration reduced them. In conclusion, our EIA proved suitable for measuring fecal TMs in mice. Our non-invasive method to assess fecal TMs can be widely used in various research disciplines like animal behavior, reproduction, animal welfare, ecology, conservation, and biomedicine.
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spelling doaj.art-6bcc8028262d4057ae17a7ed76f0314b2022-12-21T23:26:03ZengMDPI AGAnimals2076-26152020-01-0110116510.3390/ani10010165ani10010165Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive TechniquesKerstin E. Auer0Marius Kußmaul1Erich Möstl2Katharina Hohlbaum3Thomas Rülicke4Rupert Palme5Department for Biomedical Sciences, Institute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, AustriaDepartment for Biomedical Sciences, Unit of Physiology, Pathophysiology and Experimental Endocrinology, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, AustriaDepartment for Biomedical Sciences, Unit of Physiology, Pathophysiology and Experimental Endocrinology, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, AustriaDepartment of Veterinary Medicine, Institute of Animal Welfare, Animal Behavior and Laboratory Animal Science, Freie Universität Berlin, Königsweg 67, 14163 Berlin, GermanyDepartment for Biomedical Sciences, Institute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, AustriaDepartment for Biomedical Sciences, Unit of Physiology, Pathophysiology and Experimental Endocrinology, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, AustriaTestosterone is the main reproductive hormone in male vertebrates and conventional methods to measure testosterone rely on invasive blood sampling procedures. Here, we aimed to establish a non-invasive alternative by assessing testosterone metabolites (TMs) in fecal and urinary samples in mice. We performed a radiometabolism study to determine the effects of daytime and sex on the metabolism and excretion pattern of radiolabeled TMs. We performed physiological and biological validations of the applied EIA to measure TMs and assessed diurnal fluctuations in TM excretions in male and female mice and across strains. We found that males excreted significantly more radiolabeled TMs via the feces (59%) compared to females (49.5%). TM excretion patterns differed significantly between urinary and fecal samples and were affected by the daytime of &#179;H-testosterone injection. Overall, TM excretion occurred faster in urinary than fecal samples. Peak excretion of fecal TMs occurred after 8 h when animals received the <sup>3</sup>H-testosterone in the morning, or after 4 h when they received the <sup>3</sup>H-testosterone injection in the evening. Daytime had no effect on the formed TMs; however, males and females formed different types of TMs. As expected, males showed higher fecal TM levels than females. Males also showed diurnal fluctuations in their TM levels but we found no differences in the TM levels of C57BL/6J and B6D2F1 hybrid males. Finally, we successfully validated our applied EIA (measuring 17&#946;-hydroxyandrostane) by showing that hCG (human chorionic gonadotropin) administration increased TM levels, whereas castration reduced them. In conclusion, our EIA proved suitable for measuring fecal TMs in mice. Our non-invasive method to assess fecal TMs can be widely used in various research disciplines like animal behavior, reproduction, animal welfare, ecology, conservation, and biomedicine.https://www.mdpi.com/2076-2615/10/1/165testosteronemiceandrogensnon-invasivefeces
spellingShingle Kerstin E. Auer
Marius Kußmaul
Erich Möstl
Katharina Hohlbaum
Thomas Rülicke
Rupert Palme
Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive Techniques
Animals
testosterone
mice
androgens
non-invasive
feces
title Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive Techniques
title_full Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive Techniques
title_fullStr Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive Techniques
title_full_unstemmed Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive Techniques
title_short Measurement of Fecal Testosterone Metabolites in Mice: Replacement of Invasive Techniques
title_sort measurement of fecal testosterone metabolites in mice replacement of invasive techniques
topic testosterone
mice
androgens
non-invasive
feces
url https://www.mdpi.com/2076-2615/10/1/165
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AT erichmostl measurementoffecaltestosteronemetabolitesinmicereplacementofinvasivetechniques
AT katharinahohlbaum measurementoffecaltestosteronemetabolitesinmicereplacementofinvasivetechniques
AT thomasrulicke measurementoffecaltestosteronemetabolitesinmicereplacementofinvasivetechniques
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