Determining adrenocortical activity as a measure of stress in African buffalo (<em>Syncerus caffer</em>) based on faecal analysis

Article

Determining adrenocortical activity as a measure of stress in African buffalo (Syncerus caffer) based on faecal analysis

Published in: African Zoology
Volume 47 , issue 2 , 2012 , pages: 261–269
DOI: 10.1080/15627020.2012.11407558
Author(s): A. Ganswindt Mammal Research Institute, Department of Zoology and Entomology, South Africa , A.S.W. Tordiffe National Zoological Gardens of South Africa, South Africa , E. Stam Mammal Research Institute, Department of Zoology and Entomology, South Africa , M.J. Howitt National Zoological Gardens of South Africa, South Africa , F. Jori Mammal Research Institute, Department of Zoology and Entomology, South Africa

Abstract

Little is known about the levels of stress experienced by African buffalos affected by injury, disease, or socio-ecological and anthropogenic factors. To be able to start filling this gap, we examined the suitability of two 11-oxoaetiocholanolone enzyme-immunoassays (EIAs) detecting 11,17 dioxoandrostanes (11,17-DOA) as well as faecal glucocorticoid metabolites(FGMs) with a 5β-3α-ol-11-one structure (3α,11oxo-CM), respectively, for monitoring stress-related physiological responses in African buffalo. An adrenocorticotrophic hormone (ACTH) challenge in one male and one female housed at Mokopane Biodiversity Conservation Centre, South Africa, showed a threefold increase in circulating cortisol levels in a sample taken 40 min post-injection. Corresponding 11,17-DOA levels increased tenfold (female) and 15-fold (male) above baseline, and 3α,11oxo-CM concentrations increased ninefold (female) and 12-fold (male) above pre-injection levels, indicating that both EIAs are suitable for measuring FGMs in African buffalo.In addition, 11,17-DOA levels monitored during the adaptation process of individual housing revealed an up to 14-fold elevation in FGMs. Storage of faeces at ambient temperature for up to 16 h post-defecation resulted in an significant increase in 11,17-DOA levels 2 h after defecation. Finally, higher individual baseline 11,17-DOA concentrations were found in samples defecated overnight, indicating a possible diurnal effect in excretion of FGMs in African buffalo.

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