Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone Metabolites

Stress physiology is commonly employed in studies of wildlife ecology and conservation. Accordingly, we need robust and suitable methods to measure stress physiology in the field. Fecal cortisol/corticosterone metabolites (FCMs) are now increasingly being used to non-invasively evaluate adrenocortic...

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Main Authors: Andreas Eleftheriou, Rupert Palme, Rudy Boonstra
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Animals
Subjects:
Online Access:https://www.mdpi.com/2076-2615/10/7/1120
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spelling doaj-4b3771238f5a418380db87835d52a4e22020-11-25T03:16:18ZengMDPI AGAnimals2076-26152020-06-01101120112010.3390/ani10071120Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone MetabolitesAndreas Eleftheriou0Rupert Palme1Rudy Boonstra2Wildlife Biology Program, University of Montana, 32 Campus Drive, FOR 109, Missoula, MT 59812, USADepartment of Biomedical Sciences, University of Veterinary Medicine, A-1210 Vienna, AustriaCentre for the Neurobiology of Stress, University of Toronto Scarborough, 1265 Military Trail, Toronto, ON M1C 1A4, CanadaStress physiology is commonly employed in studies of wildlife ecology and conservation. Accordingly, we need robust and suitable methods to measure stress physiology in the field. Fecal cortisol/corticosterone metabolites (FCMs) are now increasingly being used to non-invasively evaluate adrenocortical activity; a measure of stress physiology. However, immunoassays that measure FCMs must be appropriately validated prior to their use and factors that can influence FCMs, such as trap-induced stress, must be considered. Deermice (Peromyscus maniculatus) are widely used in scientific studies so that developing methods that appropriately measure their adrenocortical activity is critical. In the laboratory, we tested the suitability of two enzyme immunoassays (EIAs; a corticosterone EIA, and a group-specific 5α-pregnane-3β,11β,21-triol-20-one EIA) in deermice by challenging individuals with dexamethasone and adrenocorticotropic hormone (ACTH). We found that dexamethasone suppressed FCM levels within ~10 h post injection whereas ACTH increased FCM levels within ~2 h post injection. In the field, we found that FCM levels generally increased with more time in trap confinement when using both EIAs. Although we acknowledge low sample sizes (N = 4), our results validated the two EIAs for use with FCMs from deermice.https://www.mdpi.com/2076-2615/10/7/1120captivity-induced stressenzyme immunoassayfecal glucocorticoid metabolitesphysiological stress in rodents
collection DOAJ
language English
format Article
sources DOAJ
author Andreas Eleftheriou
Rupert Palme
Rudy Boonstra
spellingShingle Andreas Eleftheriou
Rupert Palme
Rudy Boonstra
Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone Metabolites
Animals
captivity-induced stress
enzyme immunoassay
fecal glucocorticoid metabolites
physiological stress in rodents
author_facet Andreas Eleftheriou
Rupert Palme
Rudy Boonstra
author_sort Andreas Eleftheriou
title Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone Metabolites
title_short Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone Metabolites
title_full Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone Metabolites
title_fullStr Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone Metabolites
title_full_unstemmed Assessment of the Stress Response in North American Deermice: Laboratory and Field Validation of Two Enzyme Immunoassays for Fecal Corticosterone Metabolites
title_sort assessment of the stress response in north american deermice: laboratory and field validation of two enzyme immunoassays for fecal corticosterone metabolites
publisher MDPI AG
series Animals
issn 2076-2615
publishDate 2020-06-01
description Stress physiology is commonly employed in studies of wildlife ecology and conservation. Accordingly, we need robust and suitable methods to measure stress physiology in the field. Fecal cortisol/corticosterone metabolites (FCMs) are now increasingly being used to non-invasively evaluate adrenocortical activity; a measure of stress physiology. However, immunoassays that measure FCMs must be appropriately validated prior to their use and factors that can influence FCMs, such as trap-induced stress, must be considered. Deermice (Peromyscus maniculatus) are widely used in scientific studies so that developing methods that appropriately measure their adrenocortical activity is critical. In the laboratory, we tested the suitability of two enzyme immunoassays (EIAs; a corticosterone EIA, and a group-specific 5α-pregnane-3β,11β,21-triol-20-one EIA) in deermice by challenging individuals with dexamethasone and adrenocorticotropic hormone (ACTH). We found that dexamethasone suppressed FCM levels within ~10 h post injection whereas ACTH increased FCM levels within ~2 h post injection. In the field, we found that FCM levels generally increased with more time in trap confinement when using both EIAs. Although we acknowledge low sample sizes (N = 4), our results validated the two EIAs for use with FCMs from deermice.
topic captivity-induced stress
enzyme immunoassay
fecal glucocorticoid metabolites
physiological stress in rodents
url https://www.mdpi.com/2076-2615/10/7/1120
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AT rupertpalme assessmentofthestressresponseinnorthamericandeermicelaboratoryandfieldvalidationoftwoenzymeimmunoassaysforfecalcorticosteronemetabolites
AT rudyboonstra assessmentofthestressresponseinnorthamericandeermicelaboratoryandfieldvalidationoftwoenzymeimmunoassaysforfecalcorticosteronemetabolites
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