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RESEARCH ARTICLE

Faecal 11-ketoetiocholanolone measurement in Iberian red deer (Cervus elaphus hispanicus): validation of methodology using HPLC–MS/MS

C. Azorit A E , J. M. Castro B , R. Carrasco A , S. Tellado A , R. Orpez C and J. Moro D
+ Author Affiliations
- Author Affiliations

A Department of Animal, Vegetal Biology and Ecology, University of Jaén, 23071, Spain.

B Centro-Instrumentación Científico-Técnica, University of Jaén, 23071, Spain.

C Department of Chemical, Environmental and Materials Engineering, University of Jaén, 23071, Spain.

D Ministry of Agriculture, Food and Environment (National Parks), 23071, Spain.

E Corresponding autor. Email: cazorit@ujaen.es

Animal Production Science 52(8) 756-760 https://doi.org/10.1071/AN12022
Submitted: 16 January 2012  Accepted: 22 February 2012   Published: 29 May 2012

Abstract

A cortisol metabolite, 11-ketoetiocholanolone (11-k), is widely used in monitoring stress in several vertebrates, and can be detected by immunoassay. However, these assays have certain limitations with respect to specificity. Also, differences in the excretion of faecal glucocorticoid metabolites (FGM) among species and even between sexes make validation necessary in each case. Therefore, our aims were, first, to develop and validate a high-pressure liquid chromatography–tandem mass spectrometry (HPLC–MS/MS) methodology for monitoring 11-k in faeces of Iberian red deer (Cervus elaphus hispanicus), and second, to investigate the capability of our method to determine variations of this FGM in a longitudinal study. Third, and finally, we assessed the correspondence between faecal 11-k concentrations and plasma cortisol. An adrenocorticotropic hormone (ACTH) test was performed on six red deer stags translocated and kept in captivity for a week and faecal samples were collected twice a day. One single blood and faecal sample from another seven stags was also collected after 2 weeks in captivity. The results of the longitudinal study showed a first peak in 11-k 36 h after the ACTH test and handling, and a second peak at 120 h of being kept indoors. Maximum concentrations of 11-k ranged from 22.71 to 375.68 ng/g. In the second stag group, 11-k concentrations of 25.09 ± 20.53 ng/g had a correlation of r2 = 0.88 with the concentration of plasma cortisol, which was 54.6 ± 55.1 ng/mL. This technique is capable of detecting changes in the concentrations of faecal 11-k. The values determined have a good correlation with the cortisol concentration in blood, and we also detected differences in different individuals’ responses to the same stressors.

Additional keywords: monitoring, stress, faeces, glucocorticoid metabolites.


References

Broom DM, Johnson KG (1993) ‘Stress and animal welfare.’ (Chapman & Hall: London)

Ferre I, Goddard PJ, Macdonald AJ, Littlewood CA, Duff EI (1998) Effect of method of blood sample collection on adrenal activity in farmed red deer and sheep following administration of ACTH. Animal Science 67, 157–164.
Effect of method of blood sample collection on adrenal activity in farmed red deer and sheep following administration of ACTH.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXnvFOjsLs%3D&md5=6e146bba2300975bcbb886202283977cCAS |

Ganswindt A, Palme R, Heistermann M, Borragan S, Hodges JK (2003) Non-invasive assessment of adrenocortical function in the male African elephant and its relation to musth. General and Comparative Endocrinology 134, 156–166.
Non-invasive assessment of adrenocortical function in the male African elephant and its relation to musth.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXnsVWrsb0%3D&md5=d5c65fcd8f89b20ba69e84ebe5d83c3fCAS |

Goymann W, Möstl E, Hof TV, East ML, Hofer H (1999) Noninvasive faecal monitoring of glucocorticoids in spotted hyenas, Crocuta crocuta. General and Comparative Endocrinology 114, 340–348.
Noninvasive faecal monitoring of glucocorticoids in spotted hyenas, Crocuta crocuta.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXjt1aiu74%3D&md5=ecd1f3ff6fed95bbe91a26d4f26595c8CAS |

Hauser B, Deschner T, Boesch C (2008) Development of a liquid chromatography–tandem mass spectrometry method for the determination of 23 endogenous steroids in small quantities of primate urine. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences 862, 100–112.
Development of a liquid chromatography–tandem mass spectrometry method for the determination of 23 endogenous steroids in small quantities of primate urine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhsVOmtbY%3D&md5=590b83c1964f0b6e00856bae7c6c4e22CAS |

Huber S, Palme R, Arnold W (2003a) Effects of season, sex and sample collection on concentrations of faecal cortisol metabolites in red deer (Cervus elaphus). General and Comparative Endocrinology 130, 48–54.
Effects of season, sex and sample collection on concentrations of faecal cortisol metabolites in red deer (Cervus elaphus).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjtFClug%3D%3D&md5=e28eb2734f062a40cdc1a49b05f2cc97CAS |

Huber S, Palme R, Zenker W, Mostl E (2003b) Non-invasive monitoring of the adrenocortical response in red deer. The Journal of Wildlife Management 67, 258–266.
Non-invasive monitoring of the adrenocortical response in red deer.Crossref | GoogleScholarGoogle Scholar |

Ingram JR, Matthews LR, Carragher JF, Schaare PR (1997) Plasma cortisol responses to remote adrenocorticotropic hormone (ACTH) infusion in free-ranging red deer (Cervus elaphus). Domestic Animal Endocrinology 14, 63–71.
Plasma cortisol responses to remote adrenocorticotropic hormone (ACTH) infusion in free-ranging red deer (Cervus elaphus).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXkvFClug%3D%3D&md5=b875a2b5efd24bef886621092ce03e23CAS |

Keay JM, Singh J, Gaunt MC, Kaur T (2006) Faecal glucocorticoids and their metabolites as indicators of stress in various mammalian species: a literature review. Journal of Zoo and Wildlife Medicine 37, 234–244.
Faecal glucocorticoids and their metabolites as indicators of stress in various mammalian species: a literature review.Crossref | GoogleScholarGoogle Scholar |

Mikšik I, Mikulíková K, Pácha J, Kučka M, Deyl Z (2004) Application of liquid chromatography–electrospray ionization mass spectrometry for study of steroid-converting enzymes. Journal of Chromatography B 800, 145–153.
Application of liquid chromatography–electrospray ionization mass spectrometry for study of steroid-converting enzymes.Crossref | GoogleScholarGoogle Scholar |

Millspaugh JJ, Washburn BE (2004) Use of faecal glucocorticoid metabolite measures in conservation biology research: considerations for application and interpretation. General and Comparative Endocrinology 138, 189–199.
Use of faecal glucocorticoid metabolite measures in conservation biology research: considerations for application and interpretation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXnsFSjtr8%3D&md5=293e90942f75d34526ce1d281b06ee0fCAS |

Möstl E, Palme R (2002) Hormones as indicators of stress. Domestic Animal Endocrinology 23, 67–74.
Hormones as indicators of stress.Crossref | GoogleScholarGoogle Scholar |

Palme R 2005 Measuring faecal steroids: guidelines for practical application. New York Academy of Sciences 1046 7580

Palme R, Möstl E (1997) Meadurement of cortisol metabolites in faeces of sheep as a parameter of cortisol concentration in blood. International Journal of Mammalian Biology 62, 192–197.

Palme R, Robia CH, Messmann S, Hofer J, Möstl E (1999) Measurement of faecal cortisol metabolites in ruminants: a non-invasive parameter of adrenocortical function. Wiener Tierärztliche Monatsschrift 86, 237–241.

Rauh M (2009) Steroid measurement with LC–MS/MS in pediatric endocrinology. Molecular and Cellular Endocrinology 301, 272–281.
Steroid measurement with LC–MS/MS in pediatric endocrinology.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXit1OgsL0%3D&md5=20e0062894253d0b2c01e21147cf3010CAS |

Shimada K, Mitamura K, Higashi J (2001) Gas cromatography and high-performance liquid-chromatography of natural steroids. Journal of Chromatography 935, 141–172.
Gas cromatography and high-performance liquid-chromatography of natural steroids.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXot1Oiurg%3D&md5=250e7ca969730037f5550ecf2db9f006CAS |

Washburn BE, Millspaugh JJ (2002) Effects of simulated environmental conditions on glucocorticoid metabolite measurement in white-tailed deer faeces. General and Comparative Endocrinology 127, 217–222.
Effects of simulated environmental conditions on glucocorticoid metabolite measurement in white-tailed deer faeces.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XmslaltLY%3D&md5=02b3f9e17ee58a365b0a91fd4596f360CAS |

Young KM, Walker SL, Lanthier C, Waddell WT, Monfort SL, Brown JL (2004) Noninvasive monitoring of adrenocortical activity in carnivores by fecal glucocorticoid analyses. General and Comparative Endocrinology 137, 148–165.
Noninvasive monitoring of adrenocortical activity in carnivores by fecal glucocorticoid analyses.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXkt1ajsr8%3D&md5=6f70a2c25b3dfef11757779818cab221CAS |