No module Published on Offcanvas position

Hair Cortisol - Stress

Summary

 

 

The primary objective of this investigation is to develop, validate and apply the determination of cortisol, a stress related hormone, in hair as a sensitive, reliable and non-invasive measure of long term stress in caribou. Because cortisol is deposited within the hair shaft while the hair is growing (many weeks to months), hair represents a potentially superior indicator of long-term stress in comparison to other matricies (e.g. blood, urine, saliva and feces) in which cortisol levels represent stress over hours to days. In addition, hair can be collected non-invasively from live captured animals or opportunistically from animals killed during hunting activities. Hair can also be transported and stored at ambient temperature and molecules incorporated into hair may remain detectable for extended periods (from years to centuries).

 

Results

 

 


  • We have developed an enzyme-linked immunoassay-based technique to measure hair cortisol concentration (HCC) in caribou.
  • A minimum sample quantity of 100 mg hair (approximately a 2 cm by 2cm plucked or shaved patch of hair) is required for cortisol analysis.
  • In general, assay performance in Rangifer is in line with our previous work in other wildlife.
  • The high extraction efficiency (102.16 ± 5.20%) and low intra-assay coefficient of variation (CV=6.04%) indicate that the technique is accurate and precise.
  • Inter-assay CV identified in caribou is greater than that observed in our work with other species but is still within acceptable limits.
  • Parallelism between serially-diluted hair extracts and cortisol standards (r2=0.998, P< 0.0001) suggest that the assay is highly specific for cortisol.
  • A low detection limit (0.32 pg cortisol per mg hair) indicates the technique is sensitive across the range of HCC determined in caribou to date (mean= 2.22 pg/mg, range= 0.60-6.90 pg/mg, n= 125).
  • HCC varies among body regions in caribou. Owing to its low intra-region variability, we recommend collecting only shoulder or rump hair for HCC analysis.
  • HCC does not vary with sex class in captive animals.
  • HCC varies with age class in some free-ranging herds.
  • HCC in quiescent hair is not influenced by adrenocorticotropic hormone (ACTH) challenge, a procedure that mimics short-term stress.
  • Hair cortisol concentration is a promising measure of long-term stress in Rangifer.

 

Applications

 

 

 

Through this project, we are essentially developing and validating a new tool - a biomarker for long-term stress - to be used for the conservation of caribou. We anticipate this tool will be used by others to:

  • Provide baseline background data needed to quantify the impact of human land use activities.
  • Provide knowledge that is currently lacking to establish cause and effect between large-scale, human-caused environmental change and wildlife population declines.
  • Provide "early warning" of potential negative impacts on wildlife population dynamics before they occur.
  • Provide data needed to develop predictive models quantifying the response of wildlife populations in altered environments to understand how future problems can best be avoided.
  • Evaluate the efficacy of conservation actions.

 

 

 

Reports

 

 

Final report for CARMA -November 2009. Download (323kb)

 

Contacts

 

 

Marc Cattet
Canadian Cooperative Wildlife Health Centre
Western College of Veterinary Medicine
University of Saskatchewan
52 Campus Drive
Saskatoon, Saskatchewan S7N 5B4
marc.cattet "at" usask.ca
306-966-2162

 

David Janz
Dept. of Veterinary Biomedical Sciences
Western College of Veterinary Medicine
University of Saskatchewan
52 Campus Drive
Saskatoon, Saskatchewan S7N 5B4
david.janz "at" usask.ca
306-966-7434

 

Bryan Macbeth
Dept. of Veterinary Biomedical Sciences
Western College of Veterinary Medicine
University of Saskatchewan
52 Campus Drive
Saskatoon, Saskatchewan S7N 5B4
bjm197 "at" mail.usask.ca
306-966-4147